TABLE 1.

Chemical constituents in strain H3-2 extracts analyzed by GC-MS.

No.	Predicted compounds	Match	Probability (%)	RT (min)	Area (%)	Chemical formula	Activity	References
1	4,6-dimethyldodecane	774	6.5	16.020	1.93	C14H30	Antimicrobial, antioxidant	Geethalakshmi and Sarada, 2013
2	Cyclohexane, octyl-	879	47.5	19.873	1.63	C14H28	No activity reported
3	Undecane, 3,7-dimethyl-	770	7.2	20.436	0.7	C13H28	No activity reported
4	Phenol, 2,4-bis(1,1-dimethylethyl)-	884	45.1	20.769	6.89	C14H22O	Inhibitor	Kim et al., 2017
5	Benzene, 1,2,3-trimethoxy-5-(2-propenyl)-	740	37.4	21.332	1.08	C12H16O3	Antibacterial	Rossi et al., 2007
6	Hexadecane	843	17.7	22.093	0.73	C16H34	No activity reported
7	Cyclohexane,(4-methylpentyl)-	784	15.5	22.858	1.26	C12H24	No activity reported
8	9-Heptadecanone	801	79.1	25.213	0.94	C17H34O	No activity reported
9	Benzeneprop anoic acid, 3,5-bis(1,1-dimethylethyl)-4- hydroxy-,octadecyl ester	728	93.2	76.351	12.77	C35H62O3	Antimicrobial, Anticancer	Elsayed et al., 2020
10	Nonadecane, 2-methyl-	802	13.2	27.635	4.67	C20H42	Antibiofilm	Adnan, 2015
11	2-methyloctaco sane	780	15.4	29.481	2.52	C29H60	No activity reported
12	Phenol, 2,2′-methylenebis[6-(1,1-dimethylethyl)-4-methyl-	866	95.3	30.268	10.22	C23H32O2	Insecticidal	Sun et al., 2007
13	Hexadecanoic acid, 2-hydroxy-1-(hydroxymethyl)ethyl ester	786	55.9	31.434	4.79	C19H38O4	Antioxidant, anti-inflammatory, anthelmintic	Ali et al., 2015
14	Octadecanoi acid, 2-hydroxy-1-(hydroxymethyl)ethyl ester	761	46.1	34.951	4.96	C21H42O4	No activity reported