2-Naphthalenemethanol, 3,4,4a,7,8,8a-hexahydro-5-methyl-8-(1-methylethyl)-, (4aS,8S,8aR)-

Details

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Internal ID 340cf673-0492-43dd-b061-4ec61d268fe1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(4aS,8S,8aR)-5-methyl-8-propan-2-yl-3,4,4a,7,8,8a-hexahydronaphthalen-2-yl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10(2)13-6-4-11(3)14-7-5-12(9-16)8-15(13)14/h4,8,10,13-16H,5-7,9H2,1-3H3/t13-,14+,15-/m0/s1
InChI Key DFIKBBWSGFHYMP-ZNMIVQPWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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15-hydroxy-alpha-muurolene
DFIKBBWSGFHYMP-ZNMIVQPWSA-N

2D Structure

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2D Structure of 2-Naphthalenemethanol, 3,4,4a,7,8,8a-hexahydro-5-methyl-8-(1-methylethyl)-, (4aS,8S,8aR)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8673 86.73%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.6333 63.33%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9219 92.19%
OATP1B3 inhibitior + 0.8987 89.87%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9196 91.96%
P-glycoprotein inhibitior - 0.9557 95.57%
P-glycoprotein substrate - 0.8328 83.28%
CYP3A4 substrate - 0.5559 55.59%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.7119 71.19%
CYP3A4 inhibition - 0.8695 86.95%
CYP2C9 inhibition - 0.5715 57.15%
CYP2C19 inhibition - 0.6061 60.61%
CYP2D6 inhibition - 0.8485 84.85%
CYP1A2 inhibition - 0.6844 68.44%
CYP2C8 inhibition - 0.9113 91.13%
CYP inhibitory promiscuity - 0.5572 55.72%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6765 67.65%
Eye corrosion - 0.9254 92.54%
Eye irritation - 0.5881 58.81%
Skin irritation - 0.7001 70.01%
Skin corrosion - 0.9270 92.70%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3614 36.14%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.7890 78.90%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7938 79.38%
Acute Oral Toxicity (c) III 0.5985 59.85%
Estrogen receptor binding - 0.8535 85.35%
Androgen receptor binding - 0.5888 58.88%
Thyroid receptor binding - 0.6970 69.70%
Glucocorticoid receptor binding - 0.5971 59.71%
Aromatase binding - 0.8231 82.31%
PPAR gamma - 0.7891 78.91%
Honey bee toxicity - 0.9680 96.80%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9848 98.48%

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 94.70% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.47% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.46% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 91.14% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.55% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.08% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.75% 93.99%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.42% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.14% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.42% 93.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.42% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.63% 100.00%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 80.10% 97.23%

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.
Juniperus oxycedrus

Cross-Links

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PubChem 14845385
LOTUS LTS0156270
wikiData Q104977879