Ethnobotany, Phytochemistry, Biological Activities, and Health-Promoting Effects of the Genus Bulbophyllum

Abstract

The genus Bulbophyllum is of scientific interest due to the phytochemical components and diverse biological activities found across species of the genus. Most Bulbophyllum species are epiphytic and located in habitats that range from subtropical dry forests to wet montane cloud forests. In many cultures, the genus Bulbophyllum has a religious, protective, ornamenting, cosmetic, and medicinal role. Detailed investigations into the molecular pharmacological mechanisms and numerous biological effects of Bulbophyllum spp. remain ambiguous. The review focuses on an in-depth discussion of studies containing data on phytochemistry and preclinical pharmacology. Thus, the purpose of this review was to summarize the therapeutic potential of Bulbophyllum spp. biocompounds. Data were collected from several scientific databases such as PubMed and ScienceDirect, other professional websites, and traditional medicine books to obtain the necessary information. Evidence from pharmacological studies has shown that various phytoconstituents in some Bulbophyllum species have different biological health-promoting activities such as antimicrobial, antifungal, antioxidant, anti-inflammatory, anticancer, and neuroprotective. No toxicological effects have been reported to date. Future clinical trials are needed for the clinical confirmation of biological activities proven in preclinical studies. Although orchid species are cultivated for ornamental purposes and have a wide traditional use, the novelty of this review is a summary of biological actions from preclinical studies, thus supporting ethnopharmacological data.

1. Introduction

Orchids are the largest group of angiosperms consisting of nearly 28,000 species with over 736 genera [1]. Although orchids are found in natural habitats in several parts of the world, their presence is decreasing due to great demand by the population [2]. Due to habitat destruction and indiscriminate collection, Orchid species are at a steady loss [3]. One of the most represented genera is Bulbophyllum Thouars (Orchidaceae: subfamily Epidendroideae, subtribe Bulbophyllinae) with ca. 2,200 species distributed in Africa and Asia (China, Nepal, India, Thailand, Laos, and Vietnam) [4]. The taxonomic history of Bulbophyllum has been complex since its establishment [5]. The great dimension and indefinite infrageneric systematics of this genus bring significant difficulties, reducing evolution, ecology, and morphology research [6]. Taxonomists have reported at least 24 closely related genera, classified based on floral morphology [7]. Only recently, molecular biology techniques have allowed recognizing this genus as monophyletic, i.e., belonging to a common ancestor [8].

Most Bulbophyllum species are epiphytic and located in habitats that range from subtropical dry forests to wet montane cloud forests [9, 10]. They exclusively obtain water and nutrients from air, rain, and debris and thus must be able to overcome difficult environmental conditions by storing water in the pseudobulbs [11]. In addition to the economic importance attributable to ornamental uses, herbal medicinal properties of phytochemical substances of biological interest (such as flavonoids, sterols-terpenoids, and phenolic acids) in Bulbophyllum species have also been reported [12, 13]. Several studies report both the phytochemical compounds and the molecules' biological effects extracted from Bulbophyllum leaf, pseudobulb, and root, for traditional medicine treatments [14].

In a continuous effort by researchers to discover the biological activities of Bulbophyllum species, we describe and summarize recent research in ethnobotanical knowledge, phytochemistry, and pharmacological properties, along with the limitations of the research in our article.

2. Methodology

To conduct this review, data were collected from research in several scientific databases, such as PubMed and ScienceDirect, using the following MeSH terms: “Orchidaceae/chemistry∗,” “Plant Extracts/chemistry,” “Drugs, Herbal/chemistry,” “Molecular Structure,” “Anti-Inflammatory Agents/chemistry,” “Antineoplastic Agents/chemistry.” The study included documents written in English language that discussed ethnopharmacology, phytochemistry, and biological activities of these species. The taxonomy of the species has been validated according to the Plant List [15, 16].

3. Botany, Species, and Distribution

3.1. Botanical Aspects

Plants of the genus Bulbophyllum are epilithic herbs, sympodial with roots creeping over the surface of the substrate or aerial, and filamentous to fibrous [17]. Orchid plants, such as Australian Bulbophyllum minutissimum, differ in size and weight from a gram to a few millimetres (1–1.5 mm across) [18]. The stems differentiate into rhizome and pseudobulb, and the leaves may be ovate, lanceolate, or orbiculate and variable in size on an individual plant [19]. Leaves are terminal on the pseudobulb (one or several per shoots) and conduplicate to the substrate. Recently, Piazza et al. [20] studied the vegetative anatomy of 13 species of Bulbophyllum belonging to sections Didactyle and Xiphizusa to elucidate the anatomical characters between and among the sections. The results revealed the anatomical differences among the species of both lipophilic secretion sections in young leaf trichomes and the presence of xeromorphic characters. Adaptations of both species to different environmental conditions were among the main differences described by the authors [20].

The inflorescence is racemose and presents many lateral flowers emerging from the rhizome, often at the base of the pseudobulb [19]. Some orchid species in the genus Bulbophyllum show an elaborated floral architecture, in addition to their characteristic floral odours that attract and bring specific pollinators [21]. The dorsal sepal is free, similar, or smaller than the lateral sepals. The latter are united basally to each other and a column foot forms a mentum, free or fused further [19]. The lateral petals are free and smaller than the dorsal sepals, and the lip of the flowers is trilobed with a large callus. In some species, the lip flaps with the wind, to simulate a fly shaking its wings to attract insects [9]. The labellum is hinged to the tip of the column foot; the lamina is either not lobed, obscurely 3-lobed, unornamented, or with 2 longitudinal keels. The column lacks the free filament and style; the column wings are fused to the column and reduced to teeth that project beside the anther [9]. The ovary, composed of three fused carpels and the mature seed pod, opens down the middle between the lines of juncture. The ovules are arranged along the ridges inside the ovary and do not develop until sometime after the flower [9]. Orchid flowers attract specific insect species by deceiving males with an imitation signal of female odour and mimetic appearance [22]. For example, the ginger orchid (Bulbophyllum patens King) flower releases a ginger essence called zingerone that attracts fruit flies sensitive to methyl eugenol and raspberry ketone [22, 23]. Also, the flowers of Bulbophyllum apertum Schltr. release the volatile compound raspberry ketone with the function of attracting raspberry ketone-sensitive Bactrocera species [23].

The seeds of Bulbophyllum species consist of a dry, outer coat enclosing a small mass of undifferentiated cells that form a proembryo [17]. They are fusiform, spindle, and narrowly ellipsoidal shaped and less than 1 mm in length without endosperm [24]. This extremely small and light unit can easily be carried in through air currents and may travel long distances before coming to rest [17]. Seed volume is related to seed size and Bulbophyllum species, and the higher seed volume is a result of greater width rather than testa length [24]. In natural conditions, the seeds have specific germination requirements provided by mycorrhizal fungi. For instance, seeds infected by a specific fungus can either germinate or be destroyed [25]. There are different seed morphologies among the plants of the genus Bulbophyllum. For example, Bulbophyllum mysorense seeds are transparent, short, and spindle to oblong with blunt ends, and the testa cells have marginal clavate ridges, smooth on the outer face with longitudinally oriented cells resembling a twisted rope [26].

3.2. Bulbophyllum Species and Cultivation

Every year, some new Bulbophyllum species are described, making this genus grow steadily [27]. Due to the extraordinary diversity, a general description would be too extensive [1, 27]. Over 50 generic names have been proposed, in addition to Bulbophyllum [19].

In 2005, the Federal Ministry of Agriculture, Forestry, Environment, and Water Management as the CITES Management Authority of Austria elaborated three lists (names, accepted names, and the checklist) for the Bulbophyllum genus, produced by the Botanical Garden of Vienna [28]. The list is an approach to handle the vast number of species of this genus [28]. Recently, Bulbophyllum is into a single genus [7, 19]. In 2019, the World Checklist of Selected Plant Families [29] published an updated and exhaustive list that comprises over 2000 epiphytic Bulbophyllum species. There have been many efforts to split off segregate genera based on morphological characteristics. As reported by the American Orchid Society [30], some of the common Bulbophyllum species are as follows: Bulbophyllum dearei, Bulbophyllum echinolabium, Bulbophyllum falcatum, Bulbophyllum fascinator, Bulbophyllum flabellum-veneris, Bulbophyllum guttulatum, Bulbophyllum lasiochilum, Bulbophyllum lobbii, Bulbophyllum longissimum, Bulbophyllum makoyanum, Bulbophyllum medusae, and Bulbophyllum putidum. Two hybrids, Bulbophyllum Daisy Chain and Bulbophyllum Elizabeth discovered recently, are particularly attractive [30]. Among this ecological group, new taxa were also discovered: Bulbophyllum cariniflorum Reichenbach var. orlovii Aver., Bulbophyllum sonii Aver. and N. V. Duy, Bulbophyllum ustulata Aver., Bulbophyllum cariniflorum, Bulbophyllum flavescens Lindley, Bulbophyllum ovatum Seidenfaden, Bulbophyllum physocoryphum Seidenfaden, and Bulbophyllum wendlandianum Dammer.

Regarding the environmental conditions of cultivation, the warm temperature is suitable for Bulbophyllum plants that grow with a minimum of 22°C in winter, though species from temperate regions are grown 5–10 degrees cooler [30]. Light can be moderate to bright (2000 to 3500 candle feet): a higher light, which does not damage the leaves, seems to produce a better and more frequent flowering [30]. Bulbophyllum species tend to prefer a minimum of repotting using fern or cork slabs, baskets, and well-draining pots and the recommended impregnation media are sphagnum moss, coconut (flakes or coconut fibres), and tree fern both horizontally and vertically, whereas the relative humidity should be around 90% inside a greenhouse [31]. High relative humidity with a high air movement rate and constant fresh air are decisive parameters for the health and successful cultivation of the plants [31]. During the growth cycle, plants need adequate nutrition using standard fertilizers at 1/4 of the concentration given for houseplants [30]. The plants are usually rapid growers, reporting no major problems with pests. Propagation is through the division of the bulbs or via seeds of excellent germination rates [31]. Manual pollination of Bulbophyllum phalaenopsis, Bulbophyllum spies, and Bulbophyllum strontium has so far not been successful [31].

3.3. Geographical Distribution

The taxa of the genus Bulbophyllum are pantropical, spreading across Africa, Australia, India, Madagascar, Southeast Asia, and tropical South and Central America [32] (Figure 1).

Figure 1.

Geographical distribution of Bulbophyllum species.

The orchids, as epiphytes, are believed to be less adaptable to anthropogenic environmental variations than other plants [33]. The availability of the specificity host tree plays a central role in influencing the distribution and abundance of epiphytic orchids, often causing their unequal geographical distribution, even within a single tree [11].

Most of the Bulbophyllum species is epiphytes and is present in the virgin pantropical forest in the lower Montane forest at 1000 m above sea level [32]. However, a major number of species arise in the Indo-Malayan region [34]. Of 1000 species from India, 62 species are in the Northeastern region, 14 species in South India, and the remaining from other parts of India [35]. Madagascar is the hub of Bulbophyllum diversity (over 210 spp.), found mainly as epiphytes in a wide range of rainforest environments [36].

Madagascan Bulbophyllum molecular studies evidenced the existence of a monophyletic group of Late Miocene age with two major lineages: a species-rich core clade, mainly distributed in eastern rainforest of mid-to-high elevation (c. 800–1300 m), and a species-poor clade that is ecogeographically wide-ranging [37].

According to research, about 105 species of Bulbophyllum are present in China [38, 39]. Bulbophyllum Thouars is one of the largest genera among the orchid family, with around 2000 species in the tropical and subtropical zone of the world [40].

Up to date, Vietnam has documented 122 species of the genus Bulbophyllum [41]. Recent studies have allowed identifying four new species of Bulbophyllum in Vietnam, namely Bulbophyllum flavescens (sect. Aphanobulbon), Bulbophyllum ovatum (sect. Desmosanthes), Bulbophyllum physocoryphum (sect. Macrocaulia), and Bulbophyllum wendlandianum (sect. Cirrhopetalum) [40]. These species are endemic of the Indochinese Peninsula, except for Bulbophyllum flavescens, which is widely distributed in western Malesia [40]. The “vinaceous orchid” (Bulbophyllum vinaceum Ames and C. Schweinf) is a rare epiphytic plant endemic to the highlands of Borneo Island, such as the Crocker Range and Mt. Kinabalu of Sabah [21].

4. Ethnopharmacology

The usage of orchids in Ayurvedic or folklore treatment is common in many parts of the world, which raised immense attention to explore their pharmacological properties and bioactive constituents in-depth. The genus Bulbophyllum has an important role in many cultures acting as a religious, protective, ornamenting, cosmetic, and medicinal means. Leaves, pseudobulbs, and flowers of Bulbophyllum sp. have ethnobotanical importance and are used for various ailments, for both external and internal applications and administrations by tribal peoples. B. neilgherrense is an epiphytic plant used by the South Indian tribes to treat heart disease, leukoderma, skin allergy, and rheumatism; its pseudobulb is the most used part for traditional remedies.

The uses of B. scaberulum in South African traditional medicine were observed for pain-related ailments, recommending further studies to explore the chemical profile and interactions between different classes of compounds and biological/pharmacological activities.

In Cameroon, Bulbophyllum falcatum and Bulbophyllum lupulinum are used against sorcery [2]. At the same time, leaves of Bulbophyllum falcatum are used for predictions, and the whole plant of Bulbophyllum simonii is used as a luck potion [2]. Bulbophyllumshanicum is offered in many religious ceremonies and used by Kayaladies for ornamenting their hair [42]. Bulbophyllum simonii and Bulbophyllum lilacinum are mixed in body lotion to keep the body fresh and cool [2, 12].

Fluids from cleaned pseudobulbs of Bulbophyllum lilacinum are extracted by the press, kept in a sealed jar overnight, and then mixed with water and taken as a cool drink [12]. Powder of Bulbophyllum melinostachyum is recommended as anti-poisons [2].

In Zimbabwe, bark from species of the Bulbophyllum genus is tied around a fracture as a supporting pad [43]. Also, in different countries, many species of the Bulbophyllum genus are used as traditional herbal medicines (Table 1).

Table 1.

Traditional and folk medical usage of the Bulbophyllum species.

Bulbophyllum species	Country	Usage	References
Bulbophyllum albidum	India	Strengthening of a weak uterus for conception	[44]
Bulbophyllum barbigerum	Cameroon	Side pain (whole plant), ear pain (leaves)	[2]
Bulbophyllum calyptratum	Cameroon	Skin diseases (measles, poxes abscesses, rashes) (leaves), wounds, burns (whole plant)	[2]
Bulbophyllum careyanum	Nepal	Burns (pseudobulb), abortion, and recovery during childbirth (leaves)	[3]
	India	Burns (pseudobulb), abortion, and recovery during childbirth (leaves)	[45]
Bulbophyllum cariniflorum	Not specified	Induce abortion (root)	[10]
Bulbophyllum intertextum	Cameroon	Side pain (whole plant)	[2]
Bulbophyllum kaitesse	India	Cancer, inflammatory, bacterial infection (pseudobulb)	[46]
Bulbophyllum kwangtungense	China	Pulmonary tuberculosis, bleeding, fever (tuber)	[47]
	Japan	Pulmonary tuberculosis, bleeding, fever (tuber)	[47]
Bulbophyllum leopardinum	Nepal	Burns	[48]
	India	Burns	[45]
Bulbophyllum lilacinum	Bangladesh	Tiredness, anxiety, aphrodisiac, inflammation, rheumatism, hypertension, diabetes, anemia, tuberculosis, cough, asthma, jaundice, heavy menstruation, leucorrhoea, eye disease, wound (pseudobulb, whole plant)	[10, 49, 50]
Bulbophyllum modestum	Thailand	Ear infection (stem)	[51]
Bulbophyllum mutabile	Malaysia	Fever (leaves)	[52]
Bulbophyllum neilgherrense	India	Heart diseases, rheumatism, leukoderma (pseudobulb), weakness (juice), tuberculosis, chronic inflammation, fractures, scabies (whole plant)	[53–55]
	Bangladesh	Tonic	[50]
Bulbophyllum odoratissimum	Bhutan	Tuberculosis, chronic inflammation, fracture (whole plant)	[47]
	Burma	Tuberculosis, chronic inflammation, fracture (whole plant)	[47]
	China	Cough, toothache, tuberculosis, chronic inflammation, fracture (whole plant)	[47], 15]
	India	Tuberculosis, chronic inflammation, fracture (whole plant)	[45, 47]
	Laos	Tuberculosis, chronic inflammation, fracture (whole plant)	[47]
	Nepal	Tuberculosis, chronic inflammation, fracture (whole plant)	[47, 48]
	Thailand	Tuberculosis, chronic inflammation, fracture (whole plant)	[47]
	Vietnam	Tuberculosis, chronic inflammation, fracture (whole plant)	[47]
Bulbophyllum pumilum	Cameroon	Epilepsy (whole plant)	[2]
Bulbophyllum sterile	India	Rheumatism, swellings (pseudobulb)	[45]

5. Phytochemistry

The spectroscopic analyses carried out by several investigations highlighted the phytochemicals of plants belonging to the genus Bulbophyllum. Although these studies are rare, their identification results have revealed a remarkable richness in the chemical composition of the genus Bulbophyllum. The identified compounds are shown in Table 2, and the molecular chemical structures (majority compounds) are schematized by ChemDraw and are shown in Figure 2. Note in Table 2, the 17 species belong to the genus Bulbophyllum (B. odoratissimum, B. kaitense, B. weddellii, B. involutum, B. ipanemense, B. retusiusculum, B. neilgherrens, B. variegatum, B. vaginatum, B. protractum, B. reptans, B. cheiri, B. retusiusculum, B. kwangtungense, B. taeniophyllum, B. ambrosia, and B. echinolabium).

Table 2.

Phytochemistry of Bulbophyllum species.

Bulbophyllum species	Chemical classes	Compounds	References
Bulbophyllum Odoratissimum	Phenanthrene	3,7-Dihydroxy-2,4,6-trimethoxyphenanthrene	[56]
		Moscatin, 7-hydroxy-2,3,4-trimethoxy-9,10-dihydrophenanthrene, coelonin, densiflorol B, gigantol, batatasin III, tristin, vanillic acid, syringaldehyde	[57]
	Phenanthraquinone	Bulbophyllanthrone	[58]
	Biphenanthrenes	Bulbophythrin A and bulbophythrin B	[59]
	Dihydrostilbenes	5-(2-Benzo[1,3]dioxole-5-ylethyl)-6-methoxy benzo[1,3]dioxole-4-ol (1) and 5-(2-benzo[1,3]dioxole-5-ylethyl)benzo[1,3]dioxole-4,7-diol	[60]
Bulbophyllum kaitense	Ether compound	Propane, 1,1-diethoxy	[61]
	Hydrocarbon	Cyclopentane, (2-methylbutyl)
	Plasticizer compound	1,2-Benzenedicarboxylic acid, butyl 2-methylpropyl ester
	Ketone compound	2-Nonanone, 9-hydroxy
	Aromatic alcoholic compound	2,4-Dimethylcyclopentanol
	Alcoholic compound	3-Buten-2-ol
	Iodo compound	Nonane, 1-iodo
	Plasticizer compound	Didodecyl phthalate
	Alcoholic compound	3,4-Hexanediol, 2,5-dimethyl
	Ketone compound	Fluorenone, 2,3,4,7-tetramethoxy
	Triterpene	Squalene
	Bromo compound	Methyl 3-bromo-1-adamantaneacetate
	Aromatic compound	1,3-bis(Trimethylsilyl)benzene
Bulbophyllum weddellii		Furfural, 2-furanomethanol, 5-methyl-2(3H)-furanone, 2,3-dihydro-4-hydroxy-2,5-dimethyl-3-furanone, 2-methoxy-phenol, maltol, 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyrene-4-one, 1,2-benzenediol, 2,3,5,6-tetramethylphenol, 2,6-dimethoxyphenol, 4-hydroxy methyl benzoate, 4-hydroxy-3-methoxy methyl benzoate, 2,6-dimethyl-3-methoxymethyl-p-benzoquinone, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid	[62]
Bulbophyllum involutum		Furfural, 2-furanomethanol, 5-methyl-furfural, 2,3-dihydro-4-hydroxy-2,5-dimethyl-3-furanone, 2-methoxy-phenol, 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyrene-4-one, 1,2-benzenediol, 5-hydroxymethyl-2-furan-carboxyaldehyde, tetradecanoic acid, pentadecanoic acid, 14-methyl methyl pentadecanoate, 9-hexadecenoic acid, hexadecanoic acid	[62]
Bulbophyllum ipanemense		Hexanal, 2-furanomethanol, 2-pentyl-furan, 1,2-benzenediol, 2,4-decadienal-(E,Z), 2,3,5,6-tetramethylphenol, 4-decadienal-(E,E), 2,6-dimethoxyphenol, tridecanone, tridecanol, methyl tetradecanoate, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, ethyl hexadecanoate	[62]
Bulbophyllum retusiusculum	Phenylpropanoids	Retusiusine A, retusiusine B, (±)-retusiusine C, dihydroconiferyl dihydro-p-coumarate, methyl 3-(4-hydroxyphenyl) propionate, 3-(4-hydroxyphenyl)-propanoic acid, dihydroferulic acid, methyl 3-(4-methoxyphenyl) propionate, 3-(3,4-dimethoxyphenyl)-2-propenal, trans-p-coumaric acid, dihydroconiferyl alcohol	[63]
	Bibenzyl	Bulbotetusine	[64]
	Flavone C-glycoside	Apigenin 6-C-α-arabinofuranosyl 8-C-α-arabinopyranoside
Bulbophyllum neilgherrens	Alkaloids	+	[65]
	Saponin glycosides	+
	Tannins	+
	Phenols	+
	Flavonoids	+
	Steroids	+
	Reducing sugar	+
Bulbophyllum variegatum	Alcohols	2-Ethylhexanol, 2-nonanol	[66]
	Aldehydes	Nonanal, decanal
	Ketones	2-Heptanone, 2-nonanone
	Acids	Acetic acid, propanoic acid
	Sesquiterpene hydrocarbons	Beta-elemene, (E)-caryophyllene, alpha-humulene
	Nitrogenous compounds	Trimethylamine, methoxyphenyloxime, indole
	Sulphur compounds	Methyl thioacetate, benzothiazole
	Aromatic compounds	Toluene, p-cresol, p-cresyl acetate
Bulbophyllum vaginatum		Biphenanthrene, phenanthro[4,3-b]furan derivative	[67]
	Phenanthrenes	4,9-Dimethoxyphenanthrene-2,5-diol and 4,6 dimethoxyphenanthrene-2,3,7-triol, 3,4,6-trimethenanthrene-2,7-diol, 3,4-dimethoxyphenanthrene-2,7-diol (nudol), 2,4-dimethoxyphenanthrene-3,7-diol, 3,5-dimeth-oxyphenanthrene-2,7-diol, 4-methoxyphenanthrene-2,3,5-triol (fimbriol B), 4-methoxyphenan-threne-2,7-diol (flavanthrinin)	[68]
	Dihydrophenanthrenes	4-Methoxy-9,10-dihydrophenanthrene-2,3,7-triol and 4,6-dimethoxy-9,10-dihydrophenanthrene-2,3,7-trio, 9,10-dihydrophenanthrenes 3,4,6-trimethoxy-9,10-dihydrophenanthrene-2,7-diol, 4-methoxy-9,10-dihydrophenanthrene-2,7-diol (coelonin), 3,5-di-methoxy-9,10-dihydrophenanthrene-2,7-diol (6-methoxycoelonin), 3,4-dimethoxy-9,10-dihydrophenanthrene-2,7-diol (erianthridin)
	Triterpenoid	Friedelin
	Bibenzyls	3,4′-Dihydroxy-5,5′-dimethoxybibenzyl and 3,3′-dihydroxy-5-methoxybibenzyl (batatasin III)
Bulbophyllum protractum		Bulbophyllin, bulbophyllidin, batatasin III (3,3′-dihydroxy-5-methoxy bibenzyl), 3,3′,5-trimethoxybibenzyl, aloifol-I (3′,4-dihydroxy-3,5-dimethoxybibenzyl), 3,3′-dimethoxy-4,5-methylenedioxybibenzyl, flavidin (2,7-dihydroxy-9,10-dihydro-5H-phenanthro[4,5-bcd]pyran), dihydroconiferyl alcohol, stigmasterol, and sitosterol	[69]
Bulbophyllum reptans	Dimeric phenanthrenes	Reptanthrin and isoreptanthrin	[70]
	Stilbenoids	Gymnopusin, confusarin, 2,7 dihydroxy-3,4,6-trimethoxyphenanthrene, flavanthrinin, cirrhopetalanthrin
Bulbophyllum cheiri	Phenylpropanoids	Eugenol, methyl eugenol, cis-methyl isoeugenol, trans-methyl isoeugenol, 2-allyl-4,5-dimethoxyphenol, 5-allyl-1,2,4-trimethoxybenzene (euasarone), trans-3,4-dimethoxycinnamyl acetate	[71]
Bulbophyllum retusiusculum	Phenylpropanoid esters	Bobulretulate A, bobulretulate B	[72]
Bulbophyllum kwangtungense	Dihydrodibenzoxepins	7,8-Dihydro-5-hydroxy-12,13-methylenedioxy-11-methoxyldibenz[ B,F]oxepin, 7,8-dihydro-4-hydroxy-12,13-methylenedioxy-11-methoxyldibenz[ B,F]oxepin, 7,8-dihydro-3-hydroxy-12,13-methylenedioxy-11-methoxyldibenz[ B,F]oxepin, cumulatin, densiflorol A, and plicatol B	[73]
Bulbophyllum taeniophyllum	Bibenzyls	Batatasin III and cirrhopetalidin	[74]
Bulbophyllum ambrosia		Moscatin,3,7-dihydroxy-2,4-dimethoxyphenanthrene, 2,7-dihydroxy-3,4-dimethoxy-phenanthrene, 2,5-dihydroxy-4-methoxy-9,10-dihydrophenanthrene,ephemeranthol-A, 3,7-dihydroxy-2,4-dimethoxy-9,10-dihydrophenanthrene, 2,4-dihydroxy-7-methoxy-9,10-dihydrophenanthrene, coelonin, rotundatin,4′,5-dihydroxyl-3,3′-dimethoxybibenzyl, moscatilin, batatasin III, and tristin	[75]
Bulbophyllum echinolabium	Diptera attractants	Cholest-5-en-3-ol, glycerol 1-palmitate, hexadecane, tridecane, decanal, nonanal, undecane, beta-linalool, limonene, 2-hexenal	[76]
	Amino acids	L-Phenylalanine, serine, norleucine, L-threonine
	Saccharides	Alpha-D-glucopyranoside, D-turanose, sucrose, D-glucose, hydroquinone-beta-d-glucopyranoside, D-galactose, glucopyranose, 2,3,4-trihydroxybutyric acid, glycoside, alpha-methyl, ribonic acid, D-xylopyranose, D-(−)-tagatofuranose, inositol, D-ribofuranose, erythritol, D-(+)-xylose, myo-inositol, fructose
	Lipids	Stigmasterol, campesterol, cholesterol, 1-monopalmitin
	Others	Cyanuric acid, malic acid, 1-cyclohexene-1-carboxylic acid, 3,4,5-hydroxy, citric acid, alpha-hydroxyglutaric acid, mannonic acid, 1,4-lactone, benzoic acid, 3-methoxy, beta-hydroxy-beta-methylglutaric acid, p-hydroxybenzoic acid, pantothenic acid, alpha-aminoadipic acid

Figure 2.

Phytochemical compounds identified in different Bulbophyllum species schematized by ChemDraw.

Numerous chemical compounds in B. odoratissimum belong to different chemical families, in particular phenanthrene and phenanthraquinone. Chen et al. [56] identified 3,7-dihydroxy-2,4,6-trimethoxyphenanthrene, while the same author identified, 7-hydroxy-2,3,4-trimethoxy-9,10-dihydrophenanthrene, coelonin, densiflorol B, gigantol, batatasin III, tristin, vanillic acid, and syringaldehyde as major compounds in 2008 Moscatin [56]. Additionally, Xu et al. [59] identified bulbophythrin A and bulbophythrin B. B. odoratissimum was also reported to contain 5-(2-benzo[1,3]dioxole-5-ylethyl)-6-methoxy benzo[1,3]dioxole-4-ol (1) and 5-(2-benzo[1,3]dioxole-5-ylethyl)benzo[1,3]dioxole-4,7-diol [60].

The chemical compounds of Bulbophyllum weddellii, Bulbophyllum involutum, and Bulbophyllum ipanemense were characterized by Da Silva et al. [62]. In this study, several chemical compounds were identified including furfural, 2-furanomethanol, 5-methyl-2(3H)-furanone, 2,3-dihydro-4-hydroxy-2,5-dimethyl-3-furanone, 2-methoxy-phenol, maltol, 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyrene-4-one, 1,2-benzenediol, 2,3,5,6-tetramethylphenol, 2,6-dimethoxyphenol, 4-hydroxy methyl benzoate, 4-hydroxy-3-methoxy methyl benzoate, 2,6-dimethyl-3-methoxymethyl-p-benzoquinone, tetradecanoic acid, pentadecanoic acid, and hexadecanoic acid [62].

The chemical compounds of the plant B. kaitense were reported by Kalaiarasan et al. [61]. The authors observed that this plant contained numerous compounds belonging to different classes such as ether compound (propane, 1,1-diethoxy), hydrocarbon (cyclopentane, 2-methylbutyl), plasticizer compound (1,2-benzenedicarboxylic acid, butyl 2-methylpropyl ester), ketone compound (2-nonanone, 9-hydroxy), aromatic alcoholic compound (2,4-dimethylcyclopentanol), alcoholic compound (3-buten-2-ol), iodo compound (nonane, 1-iodo), plasticizer compound (didodecyl phthalate), alcoholic compound (3,4-hexanediol, 2,5-dimethyl), ketone compound (fluorenone, 2,3,4,7-tetramethoxy), triterpene (squalene), bromo compound (methyl 3-bromo-1-adamantaneacetate), and aromatic compound (1,3-bis(trimethylsilyl)benzene) [77].

The identification of chemical compounds of B. vaginatum begun in 1997 by the study of Yuan-Wah Leong et al. [68]. This work revealed the presence of different chemical compounds belonging to several chemical family such as phenanthrenes (4,9-dimethoxyphenanthrene-2,5-diol and 4,6 dimethoxyphenanthrene-2,3,7-triol,3,4,6-trimethenanthrene-2,7-diol, 3,4-dimethoxyphenanthrene-2,7-diol (nudol), 2,4 dimethoxyphenanthrene-3,7-diol, 3,5-dimeth-oxyphenanthrene-2,7-diol, 4 methoxyphenanthrene-2,3,5-triol (fimbriol B),4-methoxyphenan-threne-2,7-diol (flavanthrinin)), less bibenzyls (3,4′-dihydroxy-5,5′-dimethoxybibenzyl and 3,3′-dihydroxy-5-methoxybibenzyl) (batatasin III), and triterpenoid friedelin [68].

In the same year, B. protractum was found to contain numerous bioactive compounds including bulbophyllin, bulbophyllidin, batatasin III (3,3′-dihydroxy-5-methoxy bibenzyl), 3,3′,5-trimethoxybibenzyl, aloifol-I (3′,4-dihydroxy-3,5-dimethoxybibenzyl), 3,3′-dimethoxy-4,5-methylenedioxybibenzyl, flavidin (2,7-dihydroxy-9,10-dihydro-5H-phenanthro[4,5-bcd]pyran), dihydroconiferyl alcohol, stigmasterol, and sitosterol [69]. In addition, B. reptans was found to be rich in dimeric phenanthrenes (reptanthrin and isoreptanthrin) and stilbenoids (gymnopusin, confusarin, 2,7 dihydroxy-3,4,6-trimethoxyphenanthrene, flavanthrinin, cirrhopetalanthrin) [70].

Furthermore, B. cheiri contains several phenylpropanoids (eugenol, methyl eugenol, cis-methyl isoeugenol, trans-methyl isoeugenol, 2-allyl-4,5-dimethoxyphenol, 5-allyl-1,2,4-trimethoxybenzene (euasarone), and trans-3,4-dimethoxycinnamyl acetate) [71], while only two phenylpropanoid (bobulretulate A, bobulretulate B) esters were identified in B. retusiusculum (extracts) [72]. In contrast, six dihydrodibenzoxepins (7,8-dihydro-5-hydroxy-12,13-methylenedioxy-11-methoxyldibenz[B,F]oxepin, 7,8-dihydro-4-hydroxy-12,13-methylenedioxy-11-methoxyldibenz[B,F]oxepin, 7,8-dihydro-3-hydroxy-12,13-methylenedioxy-11-methoxyldibenz[B,F]oxepin, cumulatin, densiflorol A, and plicatol B) were identified from B. kwangtungense [73].

The extracts of B. retusiusculum contain several phytochemical compounds belonging to phenylpropanoids such as retusiusine A, retusiusine B, (±)-retusiusine C, dihydroconiferyl dihydro-p-coumarate, methyl 3-(4-hydroxyphenyl) propionate, 3-(4-hydroxyphenyl)-propionic acid, dihydroferulic acid, methyl 3-(4-methoxyphenyl) propionate, 3-(3,4-dimethoxyphenyl)-2-propenal, trans-p-coumaric acid, and dihydroconiferyl alcohol [63]. In addition, bibenzyl (bulbotetusine) and flavone C-glycoside (apigenin 6-C-α-arabinofuranosyl 8-C-α-arabinopyranoside) have also been identified in this plant [64].

The phytochemical compounds of Bulbophyllum variegatum were also identified [66]. The finding revealed the presence of several chemical families in this plant such as alcohols (2-ethylhexanol, 2-nonanol), aldehydes (nonanal and decanal), ketones (2-heptanone, 2-nonanone), acids (acetic acid, propanoic acid), sesquiterpene hydrocarbons (beta-elemene, (E)-caryophyllene, alpha-humulene), nitrogenous compounds (trimethylamine, methoxyphenyloxime, indole), sulphur compounds (methyl thioacetate, benzothiazole), and aromatic compounds (toluene, p-cresol, p-cresyl acetate) [66]. B. neilgherrens is another medicinal species of the genus Bulbophyllum. Only qualitative analysis of the chemical contents of this species was carried out by Kumari et al. [65]. The results showed the presence of different chemical classes in this plant such as alkaloids, saponin glycosides, tannins, phenols, flavonoids, and steroids [65].

Both the quantitative and qualitative differences in chemical composition across species of the genus Bulbophyllum are due to the physiology and genetics of the species. However, other factors such as climate, soil, parts used, and phenological stages of the plants can also affect the secondary metabolite synthesis in these species.

Recent studies show that chemical composition can vary within the same species, in different environments, and in extraction systems.

6. Biological Activities

6.1. Antimicrobial and Antifungal Activities

Phytochemical screening of different solvent extracts (petroleum ether, chloroform, ethanol, and water) collected from stems of terrestrial orchid B. kaitense in Kolli Hills, India, confirms the presence of terpenoids, flavonoids, reducing sugars, phenols, catechins, saponins, tannins, anthraquinone, quinine, coumarin, glycosides, and carbohydrates. Ethanol and chloroform extracts show greater antifungal activity than petroleum ether and aqueous extracts, whereas the antibacterial activity in petroleum ether extract showed less effect than that reported in chloroform, ethanol, and aqueous extracts [61].

There are many orchids with different medicinal properties and antibacterial activity. B. neilgherrense was tested for antibacterial activity against five bacterial species (Escherichia coli, Staphylococcus aureus, Bacillus pumilus, Pseudomonas aeruginosa, and Pseudomonas putida). Ethanolic, chloroform, and aqueous extracts (concentration of 5.50 w/v) from leaves and pseudobulbs were prepared for the disk diffusion method of antimicrobial sensitivity testing. The ethanolic extract of both leaves and pseudobulbs was more effective. The bacterial species P. aeruginosa and P. putida showed greater sensitivity to the pseudobulb ethanolic extract, while the ethanolic extract from leaves was effective against E. coli, S. aureus, and P. aeruginosa. However, all extracts were less effective than standard antibiotic streptomycin, when tested with the disk diffusion method in vitro [78].

In another study, Fang et al. [63] identified new phenylpropanoids in tubers of B. retusiusculum, which were then tested for their antimicrobial activities. The antimicrobial tests were performed against E. coli, B. subtilis, and Candida albicans, where kanamycin (4 μg/mL) and nystatin (4 μg/mL) were positive controls for measuring antibacterial and antifungal activity potencies, respectively. Retusiusine B exhibited potent antifungal activity against C. albicans (16 μg/mL), and (±)-retusiusine C enantiomers showed moderate antibacterial activity against B. subtilis (64 μg/mL) [63].

B. affine has moderate bactericidal activity against Staphylococcus aureus (a common cause of skin infections) but none against Bacillus subtilis, Klebsiella pneumonia, Escherichia coli, or Vibrio cholera [79].

The orchid species B. careyanum and B. leopardinum are commonly used in burn treatments [80] although antimicrobial testing has not been reported for these species. In a similar study, B. neilgherrense exhibited moderate antibacterial activity against five infectious bacterial species [78], while promising antifungal activity against ten pathogenic fungal strains was reported from the same orchid species [81].

Phenylpropanoids isolated from Bulbophyllum retusiusculum exhibited moderate antibacterial activity against Bacillus subtilis (64 μg/mL) and potent antifungal activity against Candida albicans (16 μg/mL) [63]. Bulbophyllum kaitense stem extract was also effective against 10 different bacterial strains with greater sensitivity to fungal strains [61].

In the light of these results, the antibacterial activity of orchids is a good alternative for preventing/treating infections instead of using antibiotics, which have many side effects.

6.2. Antioxidant Activity

Natural plant products have been used as poultices and/or anti-inflammatory drugs and antioxidants for many years [82, 83].

Chinsamy et al. [84] reported antioxidant activity of Bulbophyllum scaberulum higher than other South African orchid species. The overall average antioxidant activity (%ANT) of B. scaberulum pseudobulb and root extracts was higher than 90%, which might validate the use of species to treat certain inflammatory disorders.

The antioxidant effects and inhibition of acetylcholinesterase (AchE) enzyme from several indigenous orchid species (including B. Scaberulum) were evaluated. In their studies, the methanolic extracts of leaves, pseudobulbs, and roots of B. Scaberulum (similar to other orchids the extracts) showed high antioxidant potential with 100% average antioxidant activity (ANT) as compared to the standard BHT drug (95.88%), when tested with β-carotene bleaching assay. They also found that the ethanol root extract at 5 and 0.5 mg/m exhibited significant mutagenic effects comparable to the 4NQO drug. Similarly, the dichloromethane extract of roots significantly inhibit AchE with the lowest IC₅₀ value of 0.02 mg/ml, while the ethanol extract showed less activity against AchE.

Recently, Sun et al. [85] purified several compounds from B. retusiusculum whole plants. New phenanthrene, bobulretin, and two bibenzyls were evaluated against α-glucosidase activity in vitro. All three compounds showed less than 20% inhibition when tested at the final concentration of 4.37 × 10⁻⁴ mol/L.

Similarly, Bulbophyllum sp. exhibited higher antioxidant activity when compared to four other epiphytic orchids [86]. Plants of B. kaitense also presented good antioxidant activity and are considered a source of plant-derived antioxidants [87].

Polyphenols such as chrysin and pinobanksin found in orchid species of the genus Bulbophyllum have antioxidant effects [65, 88, 89], thus supporting their use in various heart diseases by the folklore traditions.

6.3. Anti-Inflammatory Activity

Nair et al. [54] used the pseudobulb powder of B. neilgherrense to examine analgesic and anti-inflammatory activities using different rat models. The pseudobulb powder mixed with honey and water revealed central analgesic activity against radiant heat-induced pain, moderate anti-inflammatory activity against carrageenan-induced acute inflammation, and mild or negligible activity against formalin-induced subacute inflammation and pain in rats. Pseudobulb contains flavonoids (chrysin and quercetin), glycosides, tannin, phenolic compounds, and calcium and may play a fundamental role in observed analgesic and anti-inflammatory activities [54].

A study run by Kumari et al. [65] reported that the pseudobulb of B. neilgherrense contains alkaloids, tannis, phenols, flavonoids, steroids, saponin glycosides, and reducing sugar (almost the same compounds as found earlier by Nair and his coworkers). The amounts of tannins, sugars, and alkaloids were 0.828%, 8.96%, and 0.3%, respectively (w/w). Of these, chrysin (a flavonoid) inhibited COX-2 expression and IL-6 signalling, indicating that B. neilgherrense pseudobulbs have anti-inflammatory potential [65].

B. kaitense was examined in vitro for its anti-inflammatory activity using the human red blood cell (HRBC) method [77]. While petroleum ether, chloroform, and aqueous extracts exhibited various anti-inflammatory activities, the ethanolic extract of B. kaitense pseudobulbs showed potent anti-inflammatory activity. As south Indian orchids, some South African medicinal orchids also demonstrated notable anti-inflammatory effects, suggesting their potential in treating inflammation and related disorders.

A study conducted by Chinsamy et al. [84] reported that the dichloromethane, ethanol, and aqueous root extract of B. scaberulum had selective and significant COX-2 inhibition effects. Inhibition was 100.00, 93.31, and 58.09%, respectively, and dichloromethane and ethanol extract IC₅₀ values against COX-2 were 1.43 and 0.44 mg/ml, respectively. Surprisingly, the dichloromethane root extracts showed a greater inhibition performance than the commercial drug galantamine for COX-2. In contrast, water extracts from leaves and pseudobulbs exhibited moderate effects on COX-2, but no effect on COX-1. The COX-2 inhibition effects of B. scaberulum suggested that it was due to condensed tannins present in the stems and/or roots [84].

Gowlis of Karnataka use a paste of pseudobulbs of Bulbophyllum neilgherrense Wight. for arthritis [90]. A study validated this trait and concluded that the pseudobulb powder had central analgesic activity against radiant heat-induced pain and moderate anti-inflammatory activity against carrageenan-induced acute inflammation [54]. The authors suggest that the potential mode of action of B. neilgherrense Wight. pseudobulb was due to the presence of flavonoids (chrysin and quercetin) in the plants [65] as several flavonoids such as hesperidin, luteolin, and quercetin have anti-inflammatory and analgesic effects [91]. Similarly, chrysin and quercetin have significant analgesic and anti-inflammatory activities [92]. However, a 50% ethanolic extract of B. gymnopus Hook f. failed to show antimicrobial or anti-inflammatory activity and did not affect either respiration, cardiovascular system, or central nervous system, in experimental animals [93].

Aqueous pseudobulb extracts of B. scaberulum showed poor or no COX-1 and COX-2 inhibition [84]. Interestingly, the organic extracts (petroleum ether, dichloromethane, and ethanol) of B. scaberulum showed higher activity in the same study.

Bulbophyllum kaitense has been used in indigenous medicine by local healers of the Kolli hills. Its anti-inflammatory validation has been reported using human red blood cell (HRBC) membrane stabilization method [46]. The HRBC membrane stabilization assay uses the HRBC method as analogous to lysosomal membrane components, and thus, the inhibition of hypotonicity or heat-induced red blood cell membrane lysis may be taken as a measure of the anti-inflammatory activity mechanism of extracts.

6.4. Anticancer Activity

Numerous studies report that Bulbophyllum species have in vitro cytotoxicity activity. The phenanthrenes isolated from Bulbophyllum odoratissimum and Bulbophyllum inconspicuum showed significant cytotoxicity against various cancer lines such as the human leukaemia cell lines K562, HL-60, and SMMC-7721 [59, 94]. Similarly, dihydrodibenzoxepins isolated from Bulbophyllum kwangtungense also exhibited antitumour activities against HeLa and K562 human tumour cell lines [73]. Chen et al. [56] isolated and studied various phenolic compounds from Bulbophyllum odoratissimum as their inhibitory ability against the growth of human leukaemia cell lines K562 and HL-60, human lung adenocarcinoma A549, human hepatoma BEL-7402, and human stomach cancer SGC-7901. The results indicated a high activity against selective cell lines, i.e., in three compounds where densiflorol was the most active compound, followed by syringaldehyde and tristin [57]. The other compounds evaluated were weak or either inactive.

Biswas et al. [95] reported that Bulbophyllum sterile petroleum ether fraction induces apoptosis in vitro and ameliorates tumour progression in vivo, suggesting that the active fractions of bulbs and roots have anticancer activity likely by inducing apoptosis through the phospho-p53-dependent pathway [95].

The extract of B. kwantungense also exhibited antitumour activity in vitro against cultivated human cervical carcinoma cells (HeLa) [96]. Chen et al. [56] isolated phenanthrene derivative 3,7-dihydroxy-2,4,6-trimethoxyphenanthrene from B. odoratissimum, and its structure was elucidated by extensive chemical transformations and nuclear magnetic resonance (NMR) spectroscopy spectrum studies. The isolated compound showed significant cytotoxicity against the growth of human leukaemia cell lines HL-60 and K562, human stomach cancer cell line SGC-7901, human hepatoma BEL-7402, and human lung adenocarcinoma A549 with IC₅₀ values of 10.02, 14.23, 1.13, 15.36, and 3.42 mg/ml, respectively.

In an investigation to evaluate the cytotoxicity of B. kwangtungense, Wu et al. [73] purified three new compounds, dihydrodibenzoxepins 7,8-dihydro-5-hydroxy-12,13-methylenedioxy-11-methoxydibenz[bf]oxepin (D5MO), 7,8-dihydro-4-hydroxy-12,13-methylenedioxy-11-methoxydibenz[bf]oxepin (D4MO), and 7,8-dihydro-3-hydroxy-12,13-methylenedioxy-11-methoxyldibenz[bf]oxepin (D3MO), along with compounds cumulatin, densiflorol A, and plicatol B. Within the compounds tested for antitumour properties, D4MO and D3MO exhibited the highest activity against HeLa cells with the IC₅₀ values of 78.3 and 61.2 μM, respectively, while activities against K562 tumour cells, D3MO, and densiflorol A showed the highest activity values with the IC₅₀ of 64.7 and 67.6 μM, respectively. In another study, two dihydrostillbenes, 3-(2-(7-methoxybenzo[d][1,3]dioxol-5-yl)ethyl)phenol (3MDP) and 6-(3-hydroxyphenethyl)benzo[d][1,3]dioxol-4-ol (6HBD), previously purified from B. odoratissimum, were synthesized via the Wittig–Horner reaction and used for developing nine synthetic analogues by Zhang et al. [97]. 3MDP and 6HBD together with their two analogues bearing an amino acid moiety in place of the phenolic OH of 3MDP and 6HBD were found to have significant anti-proliferative activity selective to two cancer cell lines, SGC-7901 and KB, with IC₅₀ value of <10.0 μM, while the other analogues showed a markedly reduced cytotoxicity towards all tumour cell lines, SGC-7901, KB, and HT-1080.

Chen et al. [57] purified nine phenolic compounds, including moscatin, 7-hydroxy-2,3,4-trimethoxy-9,10-dihydrophenanthrene, coelonin, densiflorol B, gigantol, batatasin III, tristin, vanillic acid, and syringaldehyde, from the ethyl acetate extract of B. odoratissimum whole plant and investigated the cell growth inhibition effects on different tumour cell lines such as human leukaemia cell lines K562 and HL-60, human lung adenocarcinoma A549, human hepatoma BEL-7402, and human stomach cancer SGC-7901. Except for three compounds such as densiflorol B, tristin, and syringaldehyde, all other compounds showed weak or no activity on tumour cells. Densiflorol B was the most active compound against all tumour cells showing the IC₅₀ values ranging from 0.08 to 3.52 μg/ml. Tristin displayed selective cytotoxicity against SGC-7901, with an IC₅₀ value of 2.08 μg/ml, whereas syringaldehyde exerted a strong activity against BEL-7402 cells with an IC₅₀ value of 1.54 μg/ml.

Two new dimeric phenanthrenes, bulbophythrins A and B, were then purified from B. odoratissimum, and their inhibitory ability against the growth of the same tumour cell lines was evaluated, as previously tested by Chen and his coworkers [57], with both compounds exerting significant cytotoxicity against all tumour cell lines [59]. However, bulbophythrin A exhibited some selective cytotoxicity against HL-60 and BEL-7402 with IC₅₀ values of 1.27 × 10⁻³ and 1.22 × 10⁻³ μM, respectively, whereas bulbophythrin A appeared to be most active against A549 with an IC₅₀ value of 1.18 × 10⁻³ μM, suggesting their potential use as a novel class of antitumour candidate in tumour disease.

Petroleum fraction, compared with the alcoholic extracts, from bulbs (PFB) and roots (PFR) of B. sterile, was found to be the most active in three different cancer cell lines, HCT-116, MDA-MB-231, and A549, by [95]. However, there was significant cytotoxicity in HCT-116 cells with IC₅₀ values of 94.2 and 75.7 μg/ml for PFB and PFR, respectively, likely attributed to the effects on the cell cycle G2/M phase with 32.6% and 49.4% arrest. In addition, PFB and PFR treatments showed 48% and 38% apoptosis, respectively, when tested with acridine orange/ethidium bromide (AO/EB) staining assay. Their apoptosis induction was carried out through phospho-p53-dependent pathway. Both fractions lowered tumour volume and increased life span and hepatic antioxidant level in Ehrlich ascites carcinoma (EAC) bearing mice, resulting in lower EAC-induced mortality.

In a different report by Yang et al. [64], two compounds, a flavone C-glycoside and bibenzyl purified from B. retusiusculum tubers, did not show evident cytotoxicity on six cancer cell lines, including HL-60, SMMC-7721, A549, MCF-7, and SW-480. Their IC₅₀ value was greater than 40 μM, and their noncytotoxic effects were previously thought to be attributed to their structural differences to other bibenzyl compounds previously reported to have cytotoxic effects.

6.5. Neuroprotective Effect

Alzheimer's disease (AD) is a progressive neurodegenerative disorder associated with memory impairment and cognitive deficit [98]. Various mechanisms, such as AChE inhibition, modification of monoamine levels, anti-amyloid aggregation, and antioxidant activities, are the strategies that have been employed for the amelioration of AD symptoms [99, 100]. Of these, one of the major approaches has involved addressing the levels of acetylcholine in the AD-depressed brain using AChE inhibitors [101]. Most of the currently available drugs are AchEi, and some are related to natural products with an important therapeutic strategy for the treatment of AD. Many research groups have focused their studies on naturally occurring compounds from plants as potential sources of either new or more effective AChEi. Due to the presence of flavonoids and tannins, orchid extracts that display significant effects in anti-inflammatory, antioxidant, and AChE inhibitory assays could be potential natural plant products in the inflammatory treatment of neurodegenerative disorders.

Chinsamy et al. [84] reported anticholinesterase activity (EC₅₀) for different extraction solvents as 0.02 ± 0.00 and 0.26 ± 0.007 mg/ml, respectively, in dichloromethane and ethanol root extracts of B. scaberulum. The authors also found that B. scaberulum root extract effectively inhibited AChE as compared to the commercial product galantamine.

6.6. Other Activities

Myanmar women prepare a hair tonic and shampoo by mixing ground pseudobulbs of various species of Bulbophyllum with pulverized bark, seeds, and fruit (species not identified) when washing their hair. This mixture is claimed to cure dandruff, promote hair growth, and improve hair colour [102].

Imbricatin, a stilbenoid isolated previously from Bulbophyllum and other orchid genera, was one of three isolated stilbenoids recommended for use as skin photoprotectants based on their antioxidant, anti-inflammatory, and immunomodulatory effects [103].

A summarized scheme of the most representative biological activities is summarized in Figure 3.

Figure 3.

Illustrative scheme with the most important biological activities of Bulbophyllum species and correlations with their bioactive compounds. Abbreviations and symbols: ↑, increase, ↓, decrease, COX-2, cyclooxygenase 2, IL-6, interleukin-6, and AchE, acetylcholinesterase.

7. Safety Data

No reports were found in the literature concerning health safety issues after the consumption of Bulbophyllum. This plant has been used in ethnomedicine and folk medicine by villagers in different conditions for ages; however, the toxicity profile of the Bulbophyllum species is still undiscovered. With the increasing cases of poisoning associated with the use of herbal medicines in many parts of the world in recent times [104], it is essential to ensure safety through toxicity assessment alongside active pharmacovigilance to promote their safe use and protect public health. Therefore, it is necessary to identify the risks associated with the use of such herbal plants, and in this regard, the safety of these products has become an issue of great public health importance and thus a key moment for considering it in pharmacovigilance systems.

8. Limitations and Future Perspective

The data from this review validate the use of certain orchid species in ethnopharmacology for various conditions. More comprehensive studies of the bioactive compounds of several Bulbophyllum species would open a new perspective on the relationships between chemical profiles, interactions between different classes of chemical compounds, biological properties, and correlation with geographical location. Therapeutic limitations of Bulbophyllum species are due to ignorance of long-term adverse effects, toxicity, and mutagenic potential. Future experimental pharmacological research is needed to further investigate the molecular mechanisms and action targets of the bioactive compounds contained in Bulbophyllum species. Another limitation is the lack of clinical trials.

9. Conclusion

In recent years, the genus Bulbophyllum is gaining the attention of plant researchers because of its rich phytochemical profile and variety of biological activities reported across species of the genus. Most Bulbophyllum species are epiphytic and found in habitats that range from subtropical dry forests to wet montane cloud forests. Plants belonging to the genus Bulbophyllum are mostly epilithic herbs and sympodial with roots creeping over the surface of the substrate or aerial, filamentous to fibrous. The genus Bulbophyllum has been utilized for protective, religious, cosmetic, ornamenting, and medicinal applications. Numerous investigations report the phytochemical compounds extracted from Bulbophyllum root, pseudobulb, and leaf, and their biological effect in traditional medicine treatments. Several phytochemical compounds of biological interest such as flavonoids, sterols-terpenoids, and phenolic acids have been reported in Bulbophyllum species. As summarized in the present review, the phytochemical composition of species of the genus Bulbophyllum offers insights into providing information on the antioxidant, anti-inflammatory, cytotoxic, antimicrobial, anticancer, and anticholinesterase activity. Furthermore, investigations are warranted to extract the various health-promoting phytochemicals and to identify their bioactivities, which will help to boost the utilization of Bulbophyllum species.

Data Availability

The data supporting this review are from previously reported studies and datasets, which have been cited. The processed data are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Authors' Contributions

All authors made a significant contribution to the work.