(1S,8aR)-1-methyl-6-methylidene-4-propan-2-yl-5,7,8,8a-tetrahydro-2H-naphthalene-1,4a-diol

Details

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Internal ID 64f01f93-38e9-42b7-9476-91baba1acf04
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,8aR)-1-methyl-6-methylidene-4-propan-2-yl-5,7,8,8a-tetrahydro-2H-naphthalene-1,4a-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-10(2)12-7-8-14(4,16)13-6-5-11(3)9-15(12,13)17/h7,10,13,16-17H,3,5-6,8-9H2,1-2,4H3/t13-,14+,15?/m1/s1
InChI Key USTNWHUHFGWSGY-GNXJLENFSA-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) 40.50 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,8aR)-1-methyl-6-methylidene-4-propan-2-yl-5,7,8,8a-tetrahydro-2H-naphthalene-1,4a-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.6318 63.18%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5277 52.77%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.9439 94.39%
OATP1B3 inhibitior + 0.8322 83.22%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7197 71.97%
P-glycoprotein inhibitior - 0.9267 92.67%
P-glycoprotein substrate - 0.8726 87.26%
CYP3A4 substrate + 0.5475 54.75%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.7930 79.30%
CYP2C9 inhibition - 0.7950 79.50%
CYP2C19 inhibition - 0.6312 63.12%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition - 0.7734 77.34%
CYP2C8 inhibition - 0.8466 84.66%
CYP inhibitory promiscuity - 0.7568 75.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5876 58.76%
Eye corrosion - 0.9862 98.62%
Eye irritation + 0.7169 71.69%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9383 93.83%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5677 56.77%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.5053 50.53%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6816 68.16%
Acute Oral Toxicity (c) I 0.7240 72.40%
Estrogen receptor binding - 0.6391 63.91%
Androgen receptor binding - 0.6522 65.22%
Thyroid receptor binding + 0.6455 64.55%
Glucocorticoid receptor binding - 0.6098 60.98%
Aromatase binding - 0.5678 56.78%
PPAR gamma - 0.7317 73.17%
Honey bee toxicity - 0.9272 92.72%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9883 98.83%

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 97.03% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.87% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 87.37% 94.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.86% 93.56%
CHEMBL2581 P07339 Cathepsin D 85.62% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.45% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.39% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.29% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.28% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.25% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 80.30% 90.17%

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.
Acorus calamus

Cross-Links

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PubChem 5315610
NPASS NPC127993