Research Article

Study on the Potential Mechanism of Fructus Tribuli in the Treatment of Hypertensive Vascular Remodeling Based on Network Pharmacology and Molecular Docking

Table 1

Detailed information on 17 active compounds from FT.

NumberMolecule IDMolecule nameMolecule weightOB (%)DL

FT1MOL000354Isorhamnetin316.2849.600.31
FT2MOL000359Sitosterol414.7936.910.75
FT3MOL000422Kaempferol286.2541.880.24
FT4MOL000483(Z)-3-(4-hydroxy-3-methoxy-phenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide313.38118.350.26
FT5MOL008559(2aR,2’R,4R,6aR,6bS,8aS,8bR,11aS,12aR,12bR)-4-((S)-2-(2,6-dimethylphenyl)propoxy)-5’,5’,6a,8a-tetramethyl-8-methylenedocosahydro-1H-spiro[pentaleno[2,1-a]phenanthrene-10,2’-pyran]573.0059.490.28
FT6MOL008563(3R,8S,9S,10R,13R,14R,17S)-17-((2S,5R)-5-ethyl-6-methylheptan-2-yl)-3-hydroxy-10,13-dimethyl-3,4,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-7(2H)-one428.7740.930.79
FT7MOL008567(3R,7R,8S,9S,10S,13R,14S,17R)-17-((2R,5S)-5-ethyl-6-methylheptan-2-yl)-3,10-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-7-ol414.7934.210.76
FT8MOL008568(Z)-3-(3,4-dihydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide299.35113.250.24
FT9MOL008569β-sitosterol-β-D-glucopyranoside398.7932.410.71
FT10MOL008588Terrestriamide327.36114.090.29
FT11MOL008590(2aR,2’S,4R,4’R,5’S,6aS,6bS,8aS,8bR,9S,11aR,12aR,12bR)-4,4’-dihydroxy-5’,6a,8a,9-tetramethylicosahydro-1H-spiro[pentaleno[2,1-a]phenanthrene-10,2’-pyran]-8(2H)-one444.7258.740.76
FT12MOL008593(2aR,5S,6aS,6bS,8aS,8bS,11aS,12aR,12bR)-10-isopentyl-6a,8a,9-trimethyl-2,2a,3,4,5,6,6a,6b,7,8,8a,8b,11a,12,12a,12b-hexadecahydro-1H-naphtho[2',1':4,5]indeno[2,1-b]furan-5-ol400.7139.210.84
FT13MOL007291Hecogenin430.6915.860.79
FT14MOL008581Tigogenin416.7113.830.81
FT1578177919Terrestrosin D1049.16
FT16122169314Terrestrosin K1079.18
FT17Terrestroside B1312.63