Systems Pharmacological Approach to the Effect of Bulsu-san Promoting Parturition

Table 1

65 Potential active compounds of BSS (compound with was present in both herbs).

ID	Active compounds	OB (%)	Caco-2	DL	Herb
C1	()-alpha-Terpineol	46.3	1.28	0.03	DG
C2	()-Aromadendrene	55.74	1.81	0.1	CG
C3	()-Terpinen-4-ol	81.41	1.36	0.03	CG
C4	(+)-alpha-Funebrene	52.87	1.79	0.1	CG
C5	(+)-Ledol	16.96	1.43	0.12	DG
C6	(1R,5R,7S)-4,7-Dimethyl-7-(4-methylpent-3-enyl)bicyclo3.1.1hept-3-ene	16.23	1.86	0.09	CG
C7	(1S,4aR,8aR)-1-Isopropyl-7-methyl-4-methylene-2,3,4a,5,6,8a-hexahydro-1H-naphthalene	19.8	1.86	0.08	DG
C8	(1S,4E,8E,10R)-4,8,11,11-tetramethylbicyclo8.1.0undeca-4,8-diene	21.69	1.86	0.08	CG
C9	(3E)-3-butylidene-7-hydroxy-2-benzofuran-1-one	42.17	1.03	0.08	DG
C10	(L)-alpha-Terpineol	48.8	1.39	0.03	CG
C11	(R)-Linalool	39.8	1.33	0.02	CG
C12	(Z)-Ligustilide	53.72	1.3	0.07	CG
C13	1-Acetyl-beta-carboline	67.12	1.18	0.13	CG
C14	1-beta-Ethylacrylate-7-aldehyde-beta-carboline	28.53	0.45	0.31	CG
C15	1H-Cycloprop(e)azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4aalpha,7beta,7abeta,7balpha))-	82.33	1.37	0.12	CG
C16	1-Terpineol	49.83	1.24	0.03	CG
C17	2,6-Di(phenyl)thiopyran-4-thione	69.13	1.74	0.15	DG
C18	2-[(2S,5S,6S)-6,10-Dimethylspiro4.5dec-9-en-2-yl]propan-2-ol	37.62	1.44	0.09	CG
	3-Butylidene-7-hydroxyphthalide	62.68	1	0.08	CG&DG
C20	4,7-Dihydroxy-3-butylphthalide	106.09	0.69	0.1	CG
C21	49070_FLUKA	85.51	1.29	0.12	CG
C22	4-Hydroxy-3-butylphthalide	70.31	0.9	0.08	CG
C23	58870_FLUKA	49.01	1.82	0.1	CG
	Adenine	62.81		0.03	CG&DG
C25	ADO	15.98		0.18	CG
C26	alpha-Cubebene	16.73	1.83	0.11	CG
C27	alpha-Selinene	31.81	1.82	0.1	CG
C28	Aromadendrene oxide 2	65.1	1.56	0.14	CG
	BdPh	42.44	1.32	0.07	CG&DG
C30	beta-Chamigrene	31.99	1.82	0.08	DG
	beta-Selinene	24.39	1.83	0.08	CG&DG
C32	beta-Cubebene	32.16	1.82	0.11	CG
C33	Cadinene	17.12	1.88	0.08	DG
C34	Caffeic acid	25.76	0.21	0.05	CG
C35	Carotol	149.03	1.46	0.09	CG
C36	Cedrene	51.14	1.82	0.11	CG
C37	Chuanxiongol	22.19	0.94	0.1	CG
C38	cis-Thujopsene	56.43	1.84	0.12	DG
C39	Coniferyl ferulate	4.54	0.71	0.39	DG
C40	Crysophanol	18.64	0.62	0.21	CG
C41	FA	68.96		0.71	CG
C42	Ferulic acid (CIS)	54.97	0.53	0.06	DG
C43	InChI=1/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7,11-13H,5-6,8-9H2,1-4H	55.56	1.79	0.1	DG
C44	L-Bornyl acetate	65.52	1.29	0.08	CG
C45	Methyl palmitate	18.09	1.37	0.12	CG
C46	Myricanone	40.6	0.67	0.51	CG
C47	Nicotinic acid	47.65	0.34	0.02	DG
C48	Oleic acid	33.13	1.17	0.14	CG
	Palmitic acid	19.3	1.09	0.1	CG&DG
C50	Perlolyrine	65.95	0.88	0.27	CG
C51	PLO	14.07	0.69	0.43	CG
C52	Scopoletol	27.77	0.71	0.08	DG
C53	Senkyunolide A	26.56	1.3	0.07	CG
C54	Senkyunolide G	39.52	0.63	0.08	CG
	Senkyunolide-C	46.8	0.87	0.08	CG&DG
	Senkyunolide-D	79.13	0.12	0.1	CG&DG
	Senkyunolide-E	34.4	0.55	0.08	CG&DG
C58	Senkyunolide-K	61.75	0.52	0.08	CG
C59	Sinapic acid	64.15	0.48	0.08	CG
C60	Sphingomyelin	0.31		0.51	DG
C61	Stearic acid	17.83	1.15	0.14	CG
C62	Stigmasterol	43.83	1.44	0.76	DG
C63	Succinic acid	29.62		0.01	DG
C64	Sucrose	7.17		0.23	CG
C65	Wallichilide	42.31	0.82	0.71	CG