[(3R,5S,8S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate

Details

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Internal ID 5fad7e2d-f750-4ead-935b-006086714200
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Stigmastanes and derivatives
IUPAC Name [(3R,5S,8S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H54O2/c1-9-24(21(2)3)11-10-22(4)27-15-18-32(8)29-13-12-25-20-26(34-23(5)33)14-17-30(25,6)28(29)16-19-31(27,32)7/h16,21-22,24-27,29H,9-15,17-20H2,1-8H3/t22-,24-,25+,26-,27-,29-,30+,31-,32+/m1/s1
InChI Key YFBMUIMQJYESPZ-PSGSVJHXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H54O2
Molecular Weight 470.80 g/mol
Exact Mass 470.412380961 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 10.20
Atomic LogP (AlogP) 8.99
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(3R,5S,8S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5211 52.11%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5662 56.62%
OATP2B1 inhibitior - 0.7131 71.31%
OATP1B1 inhibitior + 0.8548 85.48%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.8962 89.62%
P-glycoprotein inhibitior + 0.6831 68.31%
P-glycoprotein substrate + 0.5281 52.81%
CYP3A4 substrate + 0.6778 67.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8603 86.03%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8703 87.03%
CYP2C19 inhibition + 0.7387 73.87%
CYP2D6 inhibition - 0.9169 91.69%
CYP1A2 inhibition - 0.9248 92.48%
CYP2C8 inhibition + 0.4591 45.91%
CYP inhibitory promiscuity - 0.5066 50.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4961 49.61%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9158 91.58%
Skin irritation - 0.5214 52.14%
Skin corrosion - 0.9823 98.23%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6711 67.11%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5720 57.20%
skin sensitisation + 0.5849 58.49%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7282 72.82%
Acute Oral Toxicity (c) III 0.8186 81.86%
Estrogen receptor binding + 0.8253 82.53%
Androgen receptor binding + 0.7291 72.91%
Thyroid receptor binding + 0.5872 58.72%
Glucocorticoid receptor binding + 0.7730 77.30%
Aromatase binding + 0.6469 64.69%
PPAR gamma + 0.5548 55.48%
Honey bee toxicity - 0.7770 77.70%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5555 55.55%
Fish aquatic toxicity + 1.0000 100.00%

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 98.96% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.91% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.24% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.16% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.85% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.31% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 91.25% 97.79%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.81% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 88.39% 94.08%
CHEMBL340 P08684 Cytochrome P450 3A4 87.87% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.81% 82.69%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 87.72% 94.23%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.12% 95.89%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 84.65% 89.05%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.39% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.98% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.13% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.09% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.62% 92.62%
CHEMBL5028 O14672 ADAM10 81.00% 97.50%

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.
Neolitsea aciculata

Cross-Links

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PubChem 163011667
LOTUS LTS0268185
wikiData Q105347493