4,8a-Dimethyl-1,2,3,4,5,8-hexahydronaphthalen-4a-ol

Details

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Internal ID 7025036c-8406-4b1f-b01e-a1a9b05b23b1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 4,8a-dimethyl-1,2,3,4,5,8-hexahydronaphthalen-4a-ol
SMILES (Canonical) CC1CCCC2(C1(CC=CC2)O)C
SMILES (Isomeric) CC1CCCC2(C1(CC=CC2)O)C
InChI InChI=1S/C12H20O/c1-10-6-5-8-11(2)7-3-4-9-12(10,11)13/h3-4,10,13H,5-9H2,1-2H3
InChI Key COFTVDLZYIBNEL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O
Molecular Weight 180.29 g/mol
Exact Mass 180.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 1
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 4,8a-Dimethyl-1,2,3,4,5,8-hexahydronaphthalen-4a-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.8442 84.42%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.4843 48.43%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9459 94.59%
OATP1B3 inhibitior + 0.9652 96.52%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6099 60.99%
BSEP inhibitior - 0.8370 83.70%
P-glycoprotein inhibitior - 0.9814 98.14%
P-glycoprotein substrate - 0.9116 91.16%
CYP3A4 substrate - 0.5342 53.42%
CYP2C9 substrate - 0.5701 57.01%
CYP2D6 substrate - 0.7812 78.12%
CYP3A4 inhibition - 0.8288 82.88%
CYP2C9 inhibition - 0.8385 83.85%
CYP2C19 inhibition - 0.7142 71.42%
CYP2D6 inhibition - 0.9577 95.77%
CYP1A2 inhibition - 0.5951 59.51%
CYP2C8 inhibition - 0.9020 90.20%
CYP inhibitory promiscuity - 0.9031 90.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5618 56.18%
Eye corrosion - 0.9689 96.89%
Eye irritation + 0.5641 56.41%
Skin irritation + 0.6834 68.34%
Skin corrosion - 0.8851 88.51%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6720 67.20%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5447 54.47%
skin sensitisation + 0.6665 66.65%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.8419 84.19%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6853 68.53%
Acute Oral Toxicity (c) III 0.8267 82.67%
Estrogen receptor binding - 0.9097 90.97%
Androgen receptor binding - 0.6817 68.17%
Thyroid receptor binding - 0.8282 82.82%
Glucocorticoid receptor binding - 0.8862 88.62%
Aromatase binding - 0.7897 78.97%
PPAR gamma - 0.8094 80.94%
Honey bee toxicity - 0.9494 94.94%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9727 97.27%

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 97.95% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.50% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.34% 96.09%
CHEMBL206 P03372 Estrogen receptor alpha 88.01% 97.64%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.83% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.45% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.92% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.88% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 82.21% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.90% 95.89%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.24% 86.00%

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.
Mammillaria sphaerica

Cross-Links

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PubChem 14502825
LOTUS LTS0115698
wikiData Q104966887