alpha-Epoxysitostanol

Details

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Internal ID c2c5732a-60d3-4da8-b0bd-04ce1cf4327c
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Stigmastanes and derivatives
IUPAC Name (1S,2R,5S,7R,9S,11S,12S,15R,16R)-15-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-5-ol
SMILES (Canonical) CCC(CCC(C)C1CCC2C1(CCC3C2CC4C5(C3(CCC(C5)O)C)O4)C)C(C)C
SMILES (Isomeric) CC[C@H](CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C[C@H]4[C@@]5([C@@]3(CC[C@@H](C5)O)C)O4)C)C(C)C
InChI InChI=1S/C29H50O2/c1-7-20(18(2)3)9-8-19(4)23-10-11-24-22-16-26-29(31-26)17-21(30)12-15-28(29,6)25(22)13-14-27(23,24)5/h18-26,30H,7-17H2,1-6H3/t19-,20-,21+,22+,23-,24+,25+,26+,27-,28-,29+/m1/s1
InChI Key ZBNPKSZFWFSSQK-RUEXPLNMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H50O2
Molecular Weight 430.70 g/mol
Exact Mass 430.381080833 g/mol
Topological Polar Surface Area (TPSA) 32.80 Ų
XlogP 8.80
Atomic LogP (AlogP) 7.24
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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CHEMBL585513
5alpha,6alpha-epoxystigmastan-3beta-ol

2D Structure

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2D Structure of alpha-Epoxysitostanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.5133 51.33%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.4989 49.89%
OATP2B1 inhibitior - 0.5771 57.71%
OATP1B1 inhibitior + 0.8482 84.82%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6705 67.05%
P-glycoprotein inhibitior - 0.6087 60.87%
P-glycoprotein substrate + 0.5610 56.10%
CYP3A4 substrate + 0.7315 73.15%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.6904 69.04%
CYP3A4 inhibition - 0.8355 83.55%
CYP2C9 inhibition - 0.6038 60.38%
CYP2C19 inhibition - 0.6343 63.43%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.6590 65.90%
CYP2C8 inhibition + 0.4638 46.38%
CYP inhibitory promiscuity - 0.8686 86.86%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6592 65.92%
Eye corrosion - 0.9798 97.98%
Eye irritation - 0.9165 91.65%
Skin irritation - 0.6663 66.63%
Skin corrosion - 0.9234 92.34%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4335 43.35%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.6047 60.47%
skin sensitisation - 0.6124 61.24%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8747 87.47%
Acute Oral Toxicity (c) III 0.5080 50.80%
Estrogen receptor binding + 0.7611 76.11%
Androgen receptor binding + 0.8168 81.68%
Thyroid receptor binding + 0.6159 61.59%
Glucocorticoid receptor binding + 0.7676 76.76%
Aromatase binding + 0.6194 61.94%
PPAR gamma - 0.4924 49.24%
Honey bee toxicity - 0.6683 66.83%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9217 92.17%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.60% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.29% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.91% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.02% 97.09%
CHEMBL240 Q12809 HERG 90.04% 89.76%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.34% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.33% 91.11%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 88.32% 89.05%
CHEMBL2581 P07339 Cathepsin D 87.68% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.60% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 87.43% 95.93%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.92% 96.38%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.44% 96.61%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.86% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 84.31% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.28% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.25% 90.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.17% 97.14%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.14% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 84.05% 97.79%
CHEMBL1871 P10275 Androgen Receptor 83.40% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.33% 95.89%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 82.49% 97.31%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.73% 92.62%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.71% 97.28%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.32% 89.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Dolichandrone atrovirens
Rhododendron formosanum
Saussurea superba

Cross-Links

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PubChem 11258969
NPASS NPC94112
LOTUS LTS0080465
wikiData Q105370739