(1R,6S,8aR)-8a-methyl-4-methylidene-6-propan-2-yl-1,2,3,6,7,8-hexahydronaphthalen-1-ol

Details

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Internal ID aa3a44bf-9349-4cd1-b2f5-998877f4e7f3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1R,6S,8aR)-8a-methyl-4-methylidene-6-propan-2-yl-1,2,3,6,7,8-hexahydronaphthalen-1-ol
SMILES (Canonical) CC(C)C1CCC2(C(CCC(=C)C2=C1)O)C
SMILES (Isomeric) CC(C)[C@@H]1CC[C@]2([C@@H](CCC(=C)C2=C1)O)C
InChI InChI=1S/C15H24O/c1-10(2)12-7-8-15(4)13(9-12)11(3)5-6-14(15)16/h9-10,12,14,16H,3,5-8H2,1-2,4H3/t12-,14-,15-/m1/s1
InChI Key SKTNVTDTHGDEEV-BPLDGKMQSA-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 3.50
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 (1R,6S,8aR)-8a-methyl-4-methylidene-6-propan-2-yl-1,2,3,6,7,8-hexahydronaphthalen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.7568 75.68%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.4915 49.15%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9121 91.21%
OATP1B3 inhibitior + 0.8814 88.14%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.7928 79.28%
P-glycoprotein inhibitior - 0.9104 91.04%
P-glycoprotein substrate - 0.8658 86.58%
CYP3A4 substrate + 0.5247 52.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7337 73.37%
CYP3A4 inhibition - 0.8432 84.32%
CYP2C9 inhibition - 0.7704 77.04%
CYP2C19 inhibition - 0.6222 62.22%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.8535 85.35%
CYP2C8 inhibition - 0.8450 84.50%
CYP inhibitory promiscuity - 0.8082 80.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5996 59.96%
Eye corrosion - 0.9841 98.41%
Eye irritation - 0.6850 68.50%
Skin irritation + 0.6324 63.24%
Skin corrosion - 0.9408 94.08%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5568 55.68%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6251 62.51%
skin sensitisation + 0.6109 61.09%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7599 75.99%
Acute Oral Toxicity (c) III 0.8798 87.98%
Estrogen receptor binding - 0.8504 85.04%
Androgen receptor binding - 0.7877 78.77%
Thyroid receptor binding - 0.6243 62.43%
Glucocorticoid receptor binding - 0.6373 63.73%
Aromatase binding - 0.6868 68.68%
PPAR gamma - 0.8217 82.17%
Honey bee toxicity - 0.8873 88.73%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5062 50.62%
Fish aquatic toxicity + 0.9940 99.40%

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 94.54% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.13% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.30% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.92% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.69% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.84% 95.89%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 84.47% 92.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.77% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.14% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.99% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 80.69% 97.79%

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.
Artemisia annua

Cross-Links

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PubChem 21575628
NPASS NPC103390
LOTUS LTS0256879
wikiData Q105255025