Plant List having: β-Sitosterol

Sl. No. Plant Name
1 Aegle marmelos
2 Artocarpus heterophyllus
3 Azadirachta indica
4 Barleria cristata
5 Bauhinia purpurea
6 Bauhinia vahlii
7 Bidens pilosa
8 C. serratum
9 Callicarpa arborea
10 Callicarpa macrophylla
11 Cassia fistula
12 Cissus adnata
13 Clerodendrum serratum
14 Clerodendrum viscosum
15 Commelina benghalensis
16 Coriandum sativum
17 Debregeasia longifolia
18 Drynaria quercifolia
19 Erythrina variegata
20 Eupatorium adenophorum
21 Eupatorium birmanicum
22 Ficus carica
23 Ficus glomerata
24 Ficus hispida
25 Ficus palmata
26 Gmelina arborea
27 Goniothalamus sesquipedalis
28 Hibiscus rosa-sinensis
29 Inula cappa
30 Ipomoea batatas
31 Jatropha curcas
32 Macaranga denticulata
33 Melastoma malabathricum
34 Melia azedarach
35 Mesua ferrea
36 Musa acuminate
37 Nelumbo nucifera
38 Parkia javanica
39 Phlogacanthus curviflorn
40 Phlogacanthus thyrsiformis
41 Prunus cerasoides
42 Rhus semialata
43 Rubia cordifolia
44 Sapium baccatum
45 Sida acuta
46 Smilax glabra
47 Solanum anguivi
48 Solanum nigrum
49 Stellaria media
50 Stereospermum colais
51 Tinospora cordifolia
52 Trewia nudiflora
53 Verbena officinalis
54 Vitex negundo
55 Zanthoxylum hamiltonianum


Details of : β-Sitosterol

Canonical Smiles : CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C

Inchi Key : KZJWDPNRJALLNS-VJSFXXLFSA-N

IUPAC : (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

Pubchem ID : 222284

Smiles : CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C

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PHYSICOCHEMICAL PROPERTIES

Molecular Weight : 414.39
Volume : 482.068
Density : 0.86
nHA : 1
nHD : 1
nRot : 6
nRing : 4
Max Ring : 17
nHet: 1
fChar : 0
nRig : 20
Flexibility : 0.3
Stereo Centers : 9
TPSA : 20.23
logS : -7.052
logP: 7.663
logD7.4 : 6.329
ABSORPTION

Caco-2 Permeability : -4.756
MDCK Permeability : 0.00000862795
Pgp-inhibitor : 0.341
Pgp-substrate : 0.001
HIA : 0.004
F20% : 0.01
F30% : 0.233
DISTRIBUTION

PPB : 0.98314
VD : 1.963
BBB Penetration : 0.84
Fu : 0.0148474
METABOLISM

CYP 1A2 inhibitor : 0.044
CYP 1A2 substrate : 0.491
CYP 2C19 inhibitor : 0.074
CYP 2C19 substrate : 0.958
CYP 2C9 inhibitor : 0.096
CYP 2C9 substrate : 0.314
CYP 2D6 inhibitor : 0.005
CYP 2D6 substrate : 0.409
CYP 3A4 inhibitor : 0.202
CYP 3A4 substrate : 0.784
MEDICINAL CHEMISTRY

QED : 0.436
SAscore : 4.388
Fsp : 0.931
MCE-18 : 68.464
NPscore : 2.681
Lipinski Rule : Accepted
Pfizer Rule : Rejected
GSK Rule : Rejected
Golden Triangle : Rejected
PAINS : 0
ALARM NMR Rule : 0
BMS Rule : 0
Chelator Rule : 0
TOXICOLOGY

hERG Blockers : 0.049
H-HT : 0.16
DILI : 0.203
AMES Toxicity : 0.026
Rat Oral Acute Toxicity : 0.018
FDAMDD : 0.73
Skin Sensitization : 0.133
Carcinogencity : 0.047
Eye Corrosion : 0.003
Eye Irritation : 0.01
Respiratory Toxicity : 0.536
Bioconcentration Factor : 2.963
IGC50 : 4.984
LC50FM : 5.365
LC50DM : 6.231
NR-AR : 0.002
NR-AR-LBD: 0.003
NR-AhR : 0
NR-Aromatase : 0.015
NR-ER : 0.374
NR-ER-LBD : 0.92
NR-PPAR-gamma : 0.009
SR-ARE : 0.117
SR-ATAD5 : 0.001
SR-HSE : 0.043
SR-MMP : 0.874
SR-p53 : 0.013
Acute/Aquatic Toxicity Rule : 1
Genotoxic Carcinogenicity Rule : 0
Non Genotoxic Carcinogenicity Rule : 0
Skin Sensitization Rule : 0
Non Biodegradable Rule : 0
SureChEMBL Rule : 0
FAF-Drugs4 Rule : 0
EXCRETION

CL : 16.686
t1/2 : 0.013