(2S,4aR,5S,8S)-2,5-dimethyl-8-propan-2-yl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-ol

Details

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Internal ID d9adacbb-1395-4177-9c44-a094f6175f9b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2S,4aR,5S,8S)-2,5-dimethyl-8-propan-2-yl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-ol
SMILES (Canonical) CC1CCC(C2=CC(CCC12)(C)O)C(C)C
SMILES (Isomeric) C[C@H]1CC[C@H](C2=C[C@@](CC[C@H]12)(C)O)C(C)C
InChI InChI=1S/C15H26O/c1-10(2)12-6-5-11(3)13-7-8-15(4,16)9-14(12)13/h9-13,16H,5-8H2,1-4H3/t11-,12-,13+,15-/m0/s1
InChI Key IHEUASSNMSDWFX-XPCVCDNBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
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 (2S,4aR,5S,8S)-2,5-dimethyl-8-propan-2-yl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-ol

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 + 0.8936 89.36%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4790 47.90%
OATP2B1 inhibitior - 0.8469 84.69%
OATP1B1 inhibitior + 0.9406 94.06%
OATP1B3 inhibitior + 0.9721 97.21%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9557 95.57%
P-glycoprotein inhibitior - 0.9552 95.52%
P-glycoprotein substrate - 0.7110 71.10%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.8725 87.25%
CYP2C9 inhibition - 0.7978 79.78%
CYP2C19 inhibition - 0.7999 79.99%
CYP2D6 inhibition - 0.9302 93.02%
CYP1A2 inhibition - 0.8900 89.00%
CYP2C8 inhibition - 0.8827 88.27%
CYP inhibitory promiscuity - 0.8734 87.34%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5635 56.35%
Eye corrosion - 0.9786 97.86%
Eye irritation + 0.6466 64.66%
Skin irritation + 0.5935 59.35%
Skin corrosion - 0.9562 95.62%
Ames mutagenesis - 0.5770 57.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6578 65.78%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6973 69.73%
skin sensitisation + 0.7156 71.56%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7795 77.95%
Acute Oral Toxicity (c) III 0.7153 71.53%
Estrogen receptor binding - 0.8502 85.02%
Androgen receptor binding - 0.6792 67.92%
Thyroid receptor binding + 0.5188 51.88%
Glucocorticoid receptor binding - 0.5633 56.33%
Aromatase binding - 0.8540 85.40%
PPAR gamma - 0.8360 83.60%
Honey bee toxicity - 0.9461 94.61%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9735 97.35%

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 95.23% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.26% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.18% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.21% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.60% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.27% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.54% 100.00%
CHEMBL2581 P07339 Cathepsin D 83.19% 98.95%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.68% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.21% 97.09%

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.
Chamaecyparis obtusa

Cross-Links

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PubChem 10977056
LOTUS LTS0107209
wikiData Q105112971