(3S)-1,4-epi-3-hydroxyacorenone

Details

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Internal ID 93e6a839-53ac-4617-af17-1225952aadc6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name (1S,2S,4R,5R)-2-hydroxy-1,8-dimethyl-4-propan-2-ylspiro[4.5]dec-7-en-9-one
SMILES (Canonical) CC1C(CC(C12CC=C(C(=O)C2)C)C(C)C)O
SMILES (Isomeric) C[C@@H]1[C@H](C[C@@H]([C@]12CC=C(C(=O)C2)C)C(C)C)O
InChI InChI=1S/C15H24O2/c1-9(2)12-7-13(16)11(4)15(12)6-5-10(3)14(17)8-15/h5,9,11-13,16H,6-8H2,1-4H3/t11-,12-,13+,15+/m1/s1
InChI Key OWUULLGACRJNPQ-CXTNEJHOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S)-1,4-epi-3-hydroxyacorenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8022 80.22%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6692 66.92%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9407 94.07%
OATP1B3 inhibitior + 0.9547 95.47%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7593 75.93%
P-glycoprotein inhibitior - 0.9436 94.36%
P-glycoprotein substrate - 0.7716 77.16%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7735 77.35%
CYP2D6 substrate - 0.8637 86.37%
CYP3A4 inhibition - 0.8923 89.23%
CYP2C9 inhibition - 0.9166 91.66%
CYP2C19 inhibition - 0.7588 75.88%
CYP2D6 inhibition - 0.9507 95.07%
CYP1A2 inhibition - 0.8941 89.41%
CYP2C8 inhibition - 0.9716 97.16%
CYP inhibitory promiscuity - 0.8912 89.12%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8430 84.30%
Carcinogenicity (trinary) Non-required 0.5746 57.46%
Eye corrosion - 0.9734 97.34%
Eye irritation - 0.9210 92.10%
Skin irritation + 0.7497 74.97%
Skin corrosion - 0.9561 95.61%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3615 36.15%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6533 65.33%
skin sensitisation + 0.7158 71.58%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7889 78.89%
Acute Oral Toxicity (c) III 0.6772 67.72%
Estrogen receptor binding - 0.8304 83.04%
Androgen receptor binding - 0.4822 48.22%
Thyroid receptor binding - 0.5931 59.31%
Glucocorticoid receptor binding - 0.8521 85.21%
Aromatase binding - 0.8561 85.61%
PPAR gamma - 0.7597 75.97%
Honey bee toxicity - 0.8076 80.76%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9579 95.79%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.10% 97.25%
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.02% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.43% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.67% 85.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.96% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.65% 91.11%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.90% 93.03%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.88% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.86% 89.00%
CHEMBL2996 Q05655 Protein kinase C delta 83.16% 97.79%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.96% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.29% 93.04%
CHEMBL218 P21554 Cannabinoid CB1 receptor 82.24% 96.61%
CHEMBL1937 Q92769 Histone deacetylase 2 82.03% 94.75%
CHEMBL4208 P20618 Proteasome component C5 81.93% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.36% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.15% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.11% 97.09%

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 132500217
LOTUS LTS0115641
wikiData Q105202308