(2R,4aR,8aR)-8a-methyl-4-methylidene-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalen-2-ol

Details

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Internal ID 58410b74-4786-4afc-adf7-92651072d84d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2R,4aR,8aR)-8a-methyl-4-methylidene-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalen-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10(2)12-5-6-15(4)9-13(16)7-11(3)14(15)8-12/h5,10,13-14,16H,3,6-9H2,1-2,4H3/t13-,14-,15-/m1/s1
InChI Key VOQCANHVRSWHJK-RBSFLKMASA-N
Popularity 0 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 3.00
Atomic LogP (AlogP) 3.70
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 (2R,4aR,8aR)-8a-methyl-4-methylidene-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalen-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 + 0.9963 99.63%
Caco-2 + 0.8166 81.66%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6086 60.86%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.9016 90.16%
OATP1B3 inhibitior + 0.9030 90.30%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9067 90.67%
P-glycoprotein inhibitior - 0.9005 90.05%
P-glycoprotein substrate - 0.7953 79.53%
CYP3A4 substrate + 0.5135 51.35%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.7140 71.40%
CYP2C9 inhibition - 0.7502 75.02%
CYP2C19 inhibition - 0.5342 53.42%
CYP2D6 inhibition - 0.9326 93.26%
CYP1A2 inhibition - 0.8245 82.45%
CYP2C8 inhibition - 0.9396 93.96%
CYP inhibitory promiscuity - 0.8074 80.74%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8008 80.08%
Carcinogenicity (trinary) Non-required 0.6081 60.81%
Eye corrosion - 0.9753 97.53%
Eye irritation + 0.6969 69.69%
Skin irritation + 0.5613 56.13%
Skin corrosion - 0.9365 93.65%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5895 58.95%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5379 53.79%
skin sensitisation + 0.6812 68.12%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.5530 55.30%
Acute Oral Toxicity (c) III 0.8727 87.27%
Estrogen receptor binding - 0.8228 82.28%
Androgen receptor binding - 0.6530 65.30%
Thyroid receptor binding - 0.5966 59.66%
Glucocorticoid receptor binding - 0.6705 67.05%
Aromatase binding - 0.6571 65.71%
PPAR gamma - 0.7962 79.62%
Honey bee toxicity - 0.8672 86.72%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9912 99.12%

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 95.49% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 95.09% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.64% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.22% 93.56%
CHEMBL2581 P07339 Cathepsin D 85.76% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.46% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.38% 97.09%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.83% 85.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.77% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.31% 100.00%

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.
Cussonia bancoensis

Cross-Links

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PubChem 101032024
NPASS NPC259577