[(1aS,4aS,7S,8aR)-3-[(1R,2S,3R)-3-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-2-methyl-2-(2-oxoethyl)cyclopentyl]-4a-methyl-4-oxo-5,6,7,8-tetrahydro-1aH-naphtho[1,8a-b]oxiren-7-yl] acetate

Details

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Internal ID 8a8d3f04-d5c0-418c-84e3-eef059238c69
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids
IUPAC Name [(1aS,4aS,7S,8aR)-3-[(1R,2S,3R)-3-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-2-methyl-2-(2-oxoethyl)cyclopentyl]-4a-methyl-4-oxo-5,6,7,8-tetrahydro-1aH-naphtho[1,8a-b]oxiren-7-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H44O5/c1-18(2)19(3)8-9-20(4)24-10-11-25(28(24,6)14-15-31)23-16-26-30(35-26)17-22(34-21(5)32)12-13-29(30,7)27(23)33/h8-9,15-16,18-20,22,24-26H,10-14,17H2,1-7H3/b9-8+/t19-,20-,22-,24+,25-,26-,28-,29+,30-/m0/s1
InChI Key IGQJOYAWRCPQQD-LGZSDHHZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H44O5
Molecular Weight 484.70 g/mol
Exact Mass 484.31887450 g/mol
Topological Polar Surface Area (TPSA) 73.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.86
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1aS,4aS,7S,8aR)-3-[(1R,2S,3R)-3-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-2-methyl-2-(2-oxoethyl)cyclopentyl]-4a-methyl-4-oxo-5,6,7,8-tetrahydro-1aH-naphtho[1,8a-b]oxiren-7-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 + 0.9920 99.20%
Caco-2 - 0.6434 64.34%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7075 70.75%
OATP2B1 inhibitior - 0.8647 86.47%
OATP1B1 inhibitior + 0.8248 82.48%
OATP1B3 inhibitior + 0.8708 87.08%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9138 91.38%
P-glycoprotein inhibitior + 0.8030 80.30%
P-glycoprotein substrate + 0.5168 51.68%
CYP3A4 substrate + 0.7030 70.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8932 89.32%
CYP3A4 inhibition - 0.7612 76.12%
CYP2C9 inhibition - 0.6695 66.95%
CYP2C19 inhibition - 0.7431 74.31%
CYP2D6 inhibition - 0.9577 95.77%
CYP1A2 inhibition - 0.7454 74.54%
CYP2C8 inhibition + 0.5788 57.88%
CYP inhibitory promiscuity - 0.7255 72.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6530 65.30%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9434 94.34%
Skin irritation - 0.5962 59.62%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3756 37.56%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5821 58.21%
skin sensitisation - 0.7326 73.26%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.5346 53.46%
Acute Oral Toxicity (c) III 0.3681 36.81%
Estrogen receptor binding + 0.8109 81.09%
Androgen receptor binding + 0.7107 71.07%
Thyroid receptor binding + 0.6276 62.76%
Glucocorticoid receptor binding + 0.7277 72.77%
Aromatase binding + 0.5244 52.44%
PPAR gamma + 0.6429 64.29%
Honey bee toxicity - 0.7123 71.23%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.77% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.28% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.40% 97.25%
CHEMBL2581 P07339 Cathepsin D 94.76% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.83% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.42% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.29% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.19% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.68% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.53% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.68% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.16% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.25% 89.00%
CHEMBL5028 O14672 ADAM10 83.08% 97.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.87% 93.56%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.68% 94.23%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.22% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.96% 92.62%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.22% 82.69%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162881320
LOTUS LTS0063224
wikiData Q105112770