Plant List having: Phytosterols

Sl. No. Plant Name
1 Albizia lebbeck
2 Allium ascalonicum
3 Aloe vera
4 Anisomeles indica
5 Asparagus racemosus
6 Bauhinia variegata
7 Bergenia ciliate
8 Blumea lacera
9 Bombax ceiba
10 Cajanus cajan
11 Callicarpa macrophylla
12 Calotropis gigantea
13 Clerodendrum viscosum
14 Coccinia grandis
15 Crataeva nurvula
16 Cucumis sativus
17 Cymbopogon flexuosus
18 Cynodon dactylon
19 Datura metel
20 Dioscerea bulbifora
21 Eichhornia crassipes
22 Eupatorium odoratum
23 Euphorbia royleana
24 Ficus racemosus
25 Foeniculum vulgare
26 Garuga pinnata
27 Gloriosa superba
28 Hymenodictyon excelsum
29 Juglans regia
30 Justicia gendarussa
31 Mesua ferrea
32 Mikania cordata
33 Mirabilis jalapa
34 Momordica charantia
35 Nyctanthes arbor-tristis
36 Oroxylum indicum
37 Phyllanthus emblica
38 Phyllanthus reticulatus
39 Physalis minima
40 Picrorhiza kurrooa
41 Polyalthia longifolia
42 Polycarpon prostratum
43 Psidium guajava
44 Santalum album
45 Terminalia bellirica
46 Urtica dioica
47 Valeriana jatamansi
48 Woodfordia fruticosa


Details of : Phytosterols

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