(6S,7aS)-6-hydroxy-4,4,7a-trimethyl-1,5,6,7-tetrahydroinden-2-one

Details

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Internal ID 4df6d49f-de78-4f68-84ed-576f0d3d93f0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name (6S,7aS)-6-hydroxy-4,4,7a-trimethyl-1,5,6,7-tetrahydroinden-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H18O2/c1-11(2)5-9(14)7-12(3)6-8(13)4-10(11)12/h4,9,14H,5-7H2,1-3H3/t9-,12+/m0/s1
InChI Key JWCHFCAHCKUPOX-JOYOIKCWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18O2
Molecular Weight 194.27 g/mol
Exact Mass 194.130679813 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6S,7aS)-6-hydroxy-4,4,7a-trimethyl-1,5,6,7-tetrahydroinden-2-one

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 + 0.9295 92.95%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.5739 57.39%
OATP2B1 inhibitior - 0.8470 84.70%
OATP1B1 inhibitior + 0.9165 91.65%
OATP1B3 inhibitior + 0.9721 97.21%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7839 78.39%
P-glycoprotein inhibitior - 0.9546 95.46%
P-glycoprotein substrate - 0.8770 87.70%
CYP3A4 substrate - 0.5145 51.45%
CYP2C9 substrate - 0.7336 73.36%
CYP2D6 substrate - 0.8347 83.47%
CYP3A4 inhibition - 0.8998 89.98%
CYP2C9 inhibition - 0.8433 84.33%
CYP2C19 inhibition - 0.7503 75.03%
CYP2D6 inhibition - 0.9278 92.78%
CYP1A2 inhibition - 0.8518 85.18%
CYP2C8 inhibition - 0.9418 94.18%
CYP inhibitory promiscuity - 0.8382 83.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8848 88.48%
Carcinogenicity (trinary) Non-required 0.4704 47.04%
Eye corrosion - 0.9701 97.01%
Eye irritation + 0.8471 84.71%
Skin irritation + 0.5886 58.86%
Skin corrosion - 0.9347 93.47%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7942 79.42%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5965 59.65%
skin sensitisation + 0.7120 71.20%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.4518 45.18%
Acute Oral Toxicity (c) III 0.8216 82.16%
Estrogen receptor binding - 0.9337 93.37%
Androgen receptor binding - 0.6094 60.94%
Thyroid receptor binding - 0.8384 83.84%
Glucocorticoid receptor binding - 0.7555 75.55%
Aromatase binding - 0.7555 75.55%
PPAR gamma - 0.7410 74.10%
Honey bee toxicity - 0.9298 92.98%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8675 86.75%

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 94.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.73% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.02% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.59% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.58% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.93% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.76% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.03% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.88% 97.09%
CHEMBL4208 P20618 Proteasome component C5 80.51% 90.00%

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.
Euphorbia helioscopia

Cross-Links

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PubChem 21635123
LOTUS LTS0156153
wikiData Q105136073