(1S,4R,4aS,7S,8aR)-4a-hydroxy-1,4-dimethyl-7-prop-1-en-2-yl-1,3,4,5,6,7,8,8a-octahydronaphthalen-2-one

Details

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Internal ID 66979739-c50c-46a0-ad4c-b987912b0aeb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (1S,4R,4aS,7S,8aR)-4a-hydroxy-1,4-dimethyl-7-prop-1-en-2-yl-1,3,4,5,6,7,8,8a-octahydronaphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-9(2)12-5-6-15(17)10(3)7-14(16)11(4)13(15)8-12/h10-13,17H,1,5-8H2,2-4H3/t10-,11+,12+,13-,15+/m1/s1
InChI Key VSXHIFIYRCPZCR-KDBYPZKRSA-N
Popularity 2 references 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 (1S,4R,4aS,7S,8aR)-4a-hydroxy-1,4-dimethyl-7-prop-1-en-2-yl-1,3,4,5,6,7,8,8a-octahydronaphthalen-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 + 0.6990 69.90%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6378 63.78%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.9296 92.96%
OATP1B3 inhibitior + 0.9240 92.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.8005 80.05%
P-glycoprotein inhibitior - 0.9442 94.42%
P-glycoprotein substrate - 0.7634 76.34%
CYP3A4 substrate + 0.5606 56.06%
CYP2C9 substrate - 0.8245 82.45%
CYP2D6 substrate - 0.7981 79.81%
CYP3A4 inhibition - 0.5768 57.68%
CYP2C9 inhibition - 0.8918 89.18%
CYP2C19 inhibition - 0.8406 84.06%
CYP2D6 inhibition - 0.9535 95.35%
CYP1A2 inhibition - 0.8655 86.55%
CYP2C8 inhibition - 0.9305 93.05%
CYP inhibitory promiscuity - 0.9373 93.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5191 51.91%
Eye corrosion - 0.9908 99.08%
Eye irritation + 0.6050 60.50%
Skin irritation + 0.6091 60.91%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6069 60.69%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5217 52.17%
skin sensitisation + 0.6426 64.26%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.5523 55.23%
Acute Oral Toxicity (c) III 0.6416 64.16%
Estrogen receptor binding - 0.6643 66.43%
Androgen receptor binding - 0.5242 52.42%
Thyroid receptor binding - 0.6894 68.94%
Glucocorticoid receptor binding + 0.5902 59.02%
Aromatase binding - 0.6844 68.44%
PPAR gamma - 0.7289 72.89%
Honey bee toxicity - 0.7965 79.65%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9899 98.99%

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 95.15% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.91% 91.11%
CHEMBL1902 P62942 FK506-binding protein 1A 91.50% 97.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.97% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.01% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.24% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.27% 85.14%
CHEMBL2581 P07339 Cathepsin D 83.68% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.64% 95.56%
CHEMBL217 P14416 Dopamine D2 receptor 82.18% 95.62%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.39% 93.04%

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.
Ocotea corymbosa

Cross-Links

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PubChem 162994634
LOTUS LTS0231775
wikiData Q105292582