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. 2012 Jul 11;7(7):e39782. doi: 10.1371/journal.pone.0039782

Table 2. List of the new drug-productive species emerged in 1991–2010 together with the list of approved drugs derived from each species since the first drug approval, and the corresponding species families and their exploration status at the time of first drug approval.

New Drug ProductiveSpecies Emergedin 1991–2010 (Yearof FirstDrug Approval) Approved Drugs Derived from the Species(Year of Approval, Target(s), Therapeutic Class,Category of Source) Species Family (Yearof First DrugApproval) Exploration Status of Species Family at the Time of First Drug Approval
Period of 2001–2010
Halichondria okadai (2010) Eribulin (2010, Tubulin, anticancer, ND) Halichondriidae (2010) Newly emerged drug productive family inside existing drug productive cluster
Isaria sinclairii (2010) Fingolimod (2010, Sphingosine-1-phosphate receptor S1PR1, immunosuppression, ND) Cordycipitaceae (2010) Newly emerged drug productive family inside existing drug productive cluster
Emericella rugulosa (2007) Anidulafungin (2007, (1->3)beta-D-glucan synthase, antifungal, ND) Trichocomaceae (1942) Existing drug productive family
Sorangium cellulosum (2007) Ixabepilone (2007, Tubulin, anticancer, ND) Polyangiaceae (2007) Newly emerged drug productive family inside existing drug productive cluster
Clitopilus scyphoides (2007) Retapamulin (2007, Bacterial ribosome,antibacterial, ND) Entolomataceae (2007) Newly emerged drug productive family inside existing drug productive cluster
Ecteinascidia turbinate (2007) Trabectedin (2007, DNA, anticancer, N) Perophoridae (2007) Newly emerged drug productive family inside existing drug productive cluster
Heloderma suspectum (2005) Exenatide (2005, GLP1R, antidiabetic, ND) Helodermatidae (2005) Newly emerged drug productive family inside existing drug productive cluster
Aspergillus fumigates (2005) Fumagillin (2005, METAP2, antiparasitic, N) Trichocomaceae (1942) Existing drug productive family
Conus geographus (2005) Omega-conotoxin MVIIA (2005, Voltage-dependentN-type calcium channel, chronic pain relief, N) Conidae (2005) Newly emerged drug productive family inside existing drug productive cluster
Conus magus (2005) Omega-conotoxin MVIIA (2005, Voltage-dependentN-type calcium channel, chronic pain relief, N) Conidae (2005) Newly emerged drug productive family inside existing drug productive cluster
Streptomyces filamentosus(2003) Daptomycin (2003, Bacterial cell membrane,antibacterial, N) Streptomycetaceae (1946) Existing drug productive family
Galanthus elwesii (2002) Galantamine (2002, Acetylcholinesterase, Alzheimer’s disease, N) Amaryllidaceae (1983) Existing drug productive family
Galanthus nivalis (2002) Galantamine (2002, Acetylcholinesterase, Alzheimer’s disease, N) Amaryllidaceae (1983) Existing drug productive family
Galanthus woronowii (2002) Galantamine (2002, Acetylcholinesterase, Alzheimer’s disease, N) Amaryllidaceae (1983) Existing drug productive family
Leucojum aestivum (2002) Galantamine (2002, Acetylcholinesterase, Alzheimer’s disease, N) Amaryllidaceae (1983) Existing drug productive family
Lycoris radiate (2002) Galantamine (2002, Acetylcholinesterase, Alzheimer’s disease, N) Amaryllidaceae (1983) Existing drug productive family
Lycoris squamigera (2002) Galantamine (2002, Acetylcholinesterase, Alzheimer’s disease, N) Amaryllidaceae (1983) Existing drug productive family
Narcissus pseudonarcissus(2002) Galantamine (2002, Acetylcholinesterase, Alzheimer’s disease, N) Amaryllidaceae (1983) Existing drug productive family
Cocos nucifera (2002) Gefitinib (2002, EGFR, anticancer, S/NM), Erlotinib (2004, EGFR, anticancer, S/NM), Sunitinib (2006, VEGFR, anticancer, S/NM), Lapatinib (2007, EGFR and HER2, anticancer, S/NM), Pazopanib (2009, VEGFR, anticancer, S/NM) Arecaceae (1978) Existing drug productive family
Spinacia oleracea (2002) Gefitinib (2002, EGFR, anticancer, S/NM), Erlotinib(2004, EGFR, anticancer, S/NM), Sunitinib (2006,VEGFR, anticancer, S/NM), Lapatinib (2007, EGFRand HER2, anticancer, S/NM), Pazopanib (2009,VEGFR, anticancer, S/NM) Amaranthaceae (2002) Newly emerged drug productive family outside existing drug productive cluster
Zea mays (2002) Gefitinib (2002, EGFR, anticancer, S/NM), Erlotinib(2004, EGFR, anticancer, S/NM), Sunitinib (2006,VEGFR, anticancer, S/NM), Lapatinib (2007, EGFRand HER2, anticancer, S/NM), Pazopanib (2009,VEGFR, anticancer, S/NM) Poaceae (1984) Existing drug productive family
Coleophoma empetri (2002) Micafungin (2002, Beta-(1,3)-Glucan synthase,antifungal, ND) Coleophoma (2002) Newly emerged drug productive family outside existing drug productive cluster
Brevibacillus laterosporus(2001) Gusperimus (2001, Interleukin-2,immunosuppressant, ND) Paenibacillaceae (1942) Existing drug productive family
Lentzea albida (2001) Imatinib (2001, Abl, anticancer, ND), Nilotinib (2007, Abl, anticancer, ND) Actinosynnemataceae (1971) Existing drug productive family
Period of 1991–2000
Plectranthus barbatus (1999) Colforsin daropate (1999, Adenylate cyclase, cardiotonic, ND) Lamiaceae (1978) Existing drug productive family
Corynebacterium diphtheria (1999) Denileukin diftitox (1999, IL-2R, anticancer, B) Corynebacteriaceae (1999) Newly emerged drug productive family inside existing drug productive cluster
Lendenfeldia chondrodes (1998) Miglitol (1998, Alpha-glucosidase, antidiabetic, ND), Miglustat (2003, Glucosylceramide synthase, anti-gaucher’s disease, ND) Thorectidae (1998) Newly emerged drug productive family inside existing drug productive cluster
Morus alba (1998) Miglitol (1998, Alpha-glucosidase, antidiabetic, ND), Miglustat (2003, Glucosylceramide synthase, anti-gaucher’s disease, ND) Moraceae (1998) Newly emerged drug productive family inside existing drug productive cluster
Streptomyces toxytricini (1998) Orlistat (1998, Lipase, antiobesity, ND) Streptomycetaceae (1946) Existing drug productive family
Citrus bergamia (1997) Hesperetin (1997, Diglyceride acyltransferase, anti-cardiovascular disease, N) Rutaceae (1900) Existing drug productive family
Citrus limon (1997) Hesperetin (1997, Diglyceride acyltransferase, anti-cardiovascular disease, N) Rutaceae (1900) Existing drug productive family
Haementeria officinalis (1997) Lepirudin (1997, Thrombin, antithrombotic, ND), Bivalirudin (2000, Thrombin, anti-cardiovascular disease, ND), Hirulog (2000, Thrombin, anticoagulation, ND), Desirudin (2003, Thrombin, deep vein thrombosis, ND) Glossiphoniidae (1997) Newly emerged drug productive family inside existing drug productive cluster
Hirudo medicinalis (1997) Lepirudin (1997, Thrombin, antithrombotic, ND), Bivalirudin (2000, Thrombin, anti-cardiovascular disease, ND), Hirulog (2000, Thrombin, anticoagulation, ND), Desirudin (2003, Thrombin, deep vein thrombosis, ND) Hirudinidae (1997) Newly emerged drug productive family inside existing drug productive cluster
Artemisia dracunculus (1996) Latanoprost (1996, PGF receptor, antiglaucoma, ND), Bimatoprost (2001, PGF receptor, antiglaucoma, ND), Travoprost (2001, PGF receptor, antiglaucoma, ND) Asteraceae (1975) Existing drug productive family
Mus musculus (1995) Edrecolomab (1995, EpCAM, anticancer, B), Daclizumab (1997, IL-2R, immunosuppressant, B), Palivizumab (1998, Fusion glycoprotein, antiviral, B), Trastuzumab (1998, HER-2, anticancer, B), Alemtuzumab (2001, CD52, anticancer, B), Efalizumab (2003, CD11a subunit of lymphocyte function-associated antigen 1, antipsoriatic, B), Omalizumab (2003, Human immunoglobulin E, antiasthmatic, B), Bevacizumab (2004, VEGF-A, anticancer, B), Natalizumab (2004, Alpha-4 integrin, anti-inflammatory, B), Tocilizumab (2005, IL-6R, immunosuppressant, B), Nimotuzumab (2006, EGFR, anticancer, B), Ranibizumab (2006, VEGF-A, anti-angiogenic, B) Muridae (1994) Newly emerged drug productive family inside existing drug productive cluster
Aspergillus unilateralis (1995) Mycophenolate mofetil (1995, IMPDH2, immunosuppressant, ND), Mycophenolic acid (2003, IMPDH2, immunosuppressant, N) Trichocomaceae (1942) Existing drug productive family
Byssochlamys nivea (1995) Mycophenolate mofetil (1995, IMPDH2, immunosuppressant, ND), Mycophenolic acid (2003, IMPDH2, immunosuppressant, N) Trichocomaceae (1942) Existing drug productive family
Penicillium bialowiezense (1995) Mycophenolate mofetil (1995, IMPDH2, immunosuppressant, ND), Mycophenolic acid (2003, IMPDH2, immunosuppressant, N) Trichocomaceae (1942) Existing drug productive family
Penicillium carneum (1995) Mycophenolate mofetil (1995, IMPDH2, immunosuppressant, ND), Mycophenolic acid (2003, IMPDH2, immunosuppressant, N) Trichocomaceae (1942) Existing drug productive family
Penicillium fagi (1995) Mycophenolate mofetil (1995, IMPDH2, immunosuppressant, ND), Mycophenolic acid (2003, IMPDH2, immunosuppressant, N) Trichocomaceae (1942) Existing drug productive family
Penicillium roqueforti (1995) Mycophenolate mofetil (1995, IMPDH2, immunosuppressant, ND), Mycophenolic acid (2003, IMPDH2, immunosuppressant, N) Trichocomaceae (1942) Existing drug productive family
Streptomyces argenteolus subsp. Toyonakensis (1995) Saquinavir mesylate (1995, HIV-1 protease, anti-virus, S*/NM), Indinavir sulfate (1996, HIV-1 protease, anti-virus, S*/NM), Ritonavir (1996, HIV-1 protease, anti-virus, S*/NM), Neflinavir mesylate (1997, HIV-1 protease, anti-virus, S*/NM), Amprenavir (1999, HIV-1 protease, anti-virus, S*/NM), Lopinavir (2000, HIV-1 protease, anti-virus, S*/NM) Streptomycetaceae (1946) Existing drug productive family
Streptomyces testaceus (1995) Saquinavir mesylate (1995, HIV-1 protease, anti-virus, S*/NM), Indinavir sulfate (1996, HIV-1 protease, anti-virus, S*/NM), Ritonavir (1996, HIV-1 protease, anti-virus, S*/NM), Neflinavir mesylate (1997, HIV-1 protease, anti-virus, S*/NM), Amprenavir (1999, HIV-1 protease, anti-virus, S*/NM), Lopinavir (2000, HIV-1 protease, anti-virus, S*/NM) Streptomycetaceae (1946) Existing drug productive family
Camptotheca acuminate (1994) Irinotecan (1994, DNA topoisomerase I, anticancer, ND), Topotecan (1996, DNA topoisomerase I, anticancer, ND) Cornaceae (1994) Newly emerged drug productive family outside existing drug productive cluster
Mappia foetida (1994) Irinotecan (1994, DNA topoisomerase I, anticancer, ND), Topotecan (1996, DNA topoisomerase I, anticancer, ND), Belotecan (2004, DNA topoisomerase I, anticancer, ND), Sphingosomal topotecan (2007, DNA topoisomerase I, anticancer, ND) Icacinaceae (1994) Newly emerged drug productive family inside existing drug productive cluster
Ophiorrhiza pumila (1994) Irinotecan (1994, DNA topoisomerase I, anticancer, ND), Topotecan (1996, DNA topoisomerase I, anticancer, ND), Belotecan (2004, DNA topoisomerase I, anticancer, ND), Sphingosomal topotecan (2007, DNA topoisomerase I, anticancer, ND) Rubiaceae (1940) Existing drug productive family
Rattus norvegicus (1994) Losartan potassium (1994, AGTR1, antihypertensive, S/NM), Valsartan (1996, AGTR1, antihypertensive, S/NM), Candesartan cilexetil (1997, AGTR2, antihypertensive, S/NM), Eprosartan (1997, AGTR1, antihypertensive, S/NM), Irbesartan (1997, AGTR1, antihypertensive, S/NM), Telmisartan (1999, AGTR1, antihypertensive, S/NM), Olmesartan medoxil (2002, Angiotensin II receptor 1, antihypertensive, S/NM) Muridae (1994) Newly emerged drug productive family inside existing drug productive cluster
Erwinia chrysanthemi (1994) Pegaspargase (1994, L-asparaginase, anticancer, B) Enterobacteriaceae (1969) Existing drug productive family
Streptomyces hygroscopicus (1994) Voglibose (1994, Alpha-glucosidase, antidiabetic, N), Zotarolimus (1996, mTOR, anticancer, ND), Sirolimus (1999, mTOR, immunosuppressive, N), Pimecrolimus (2001, Calcineurin, immunomodulating, ND), Vorinostat (2006, HDAC, anticancer, ND), Temsirolimus (2007, mTOR, anticancer, ND), Everolimus (2009, mTOR, anticancer, ND) Streptomycetaceae (1946) Existing drug productive family
Corylus avellana (1993) Paclitaxel (1993, Tubulin, anticancer, N), Cabazitaxel (2010, Tubulin, anticancer, ND) Betulaceae (1993) Newly emerged drug productive family inside existing drug productive cluster
Seimatoantlerium tepuiense (1993) Paclitaxel (1993, Tubulin, anticancer, N), Cabazitaxel (2010, Tubulin, anticancer, ND) Amphisphaeriaceae (1993) Newly emerged drug productive family outside existing drug productive cluster
Taxus baccata (1993) Paclitaxel (1993, Tubulin, anticancer, N), Docetaxel (1995, Tubulin, anticancer, ND), Cabazitaxel (2010, Tubulin, anticancer, ND) Taxaceae (1993) Newly emerged drug productive family inside existing drug productive cluster
Taxus brevifolia (1993) Paclitaxel (1993, Tubulin, anticancer, N), Docetaxel (1995, Tubulin, anticancer, ND), Cabazitaxel (2010, Tubulin, anticancer, ND) Taxaceae (1993) Newly emerged drug productive family inside existing drug productive cluster
Taxus wallichiana (1993) Paclitaxel (1993, Tubulin, anticancer, N), Docetaxel (1995, Tubulin, anticancer, ND), Cabazitaxel (2010, Tubulin, anticancer, ND) Taxaceae (1993) Newly emerged drug productive family inside existing drug productive cluster
Streptomyces tsukubaensis (1993) Tacrolimus (1993, Calcineurin, immunosuppressant, N) Streptomycetaceae (1946) Existing drug productive family
Larrea tridentate (1992) Masoprocol (1992, 5-LOX, anticancer, N) Zygophyllaceae (1978) Existing drug productive family
Agaricus bisporus (1991) Calcipotriol (1991, Vitamin D receptor, antipsoriatic, ND), Tacalcitol (1993, Vitamin D receptor, antipsoriatic, ND), Paricalcitol (1998, Vitamin D receptor, calcium metabolism, ND), Doxercalciferol (1999, Vitamin D receptor, calcium metabolism, ND) Agaricaceae (1991) Newly emerged drug productive family inside existing drug productive cluster
Leontice leontopetalum (1991) Doxacurium chloride (1991, CHRNA2, muscle relaxant, S*), Mivacurium chloride (1992, CHRNA2, muscle relaxant, S*), Cisatracurium besilate (1995, nAChR, muscle relaxant, S*) Berberidaceae (1978) Existing drug productive family
Callistemon citrinus (1991) Nitisinone (1991, 4HPPD, antityrosinaemia, ND) Myrtaceae (1991) Newly emerged drug productive family inside existing drug productive cluster

The categories of drug source are based on the definition of Newman and Cragg [2]: “B” Biological; usually a large (>45 residues) peptide or protein either isolated from an organism/cell line or produced by biotechnological means in a surrogate host,“N” Natural product, “ND” Derived from a natural product and is usually a semisynthetic modification, “S*” Made by total synthesis, but the pharmacophore is/was from a natural product.“V” Vaccine, “NM” Natural product mimic.