(8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulen-6-yl)methanol

Details

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Internal ID 2e41d507-7754-4865-bf5d-c10cb3a5d622
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulen-6-yl)methanol
SMILES (Canonical) CC(=C)C1CCC2(C1CCC(=CC2)CO)C
SMILES (Isomeric) CC(=C)C1CCC2(C1CCC(=CC2)CO)C
InChI InChI=1S/C15H24O/c1-11(2)13-7-9-15(3)8-6-12(10-16)4-5-14(13)15/h6,13-14,16H,1,4-5,7-10H2,2-3H3
InChI Key AUASPLXQOHHJLG-UHFFFAOYSA-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 3.90
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulen-6-yl)methanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.8468 84.68%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.8599 85.99%
OATP2B1 inhibitior - 0.8452 84.52%
OATP1B1 inhibitior + 0.9295 92.95%
OATP1B3 inhibitior + 0.9306 93.06%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8255 82.55%
P-glycoprotein inhibitior - 0.9244 92.44%
P-glycoprotein substrate - 0.7921 79.21%
CYP3A4 substrate + 0.5134 51.34%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.8053 80.53%
CYP2C9 inhibition - 0.6470 64.70%
CYP2C19 inhibition - 0.7298 72.98%
CYP2D6 inhibition - 0.8970 89.70%
CYP1A2 inhibition - 0.7333 73.33%
CYP2C8 inhibition - 0.6583 65.83%
CYP inhibitory promiscuity - 0.8111 81.11%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6203 62.03%
Eye corrosion - 0.9151 91.51%
Eye irritation + 0.7272 72.72%
Skin irritation - 0.7173 71.73%
Skin corrosion - 0.9670 96.70%
Ames mutagenesis - 0.7237 72.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4015 40.15%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5726 57.26%
skin sensitisation + 0.6669 66.69%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7370 73.70%
Acute Oral Toxicity (c) III 0.7353 73.53%
Estrogen receptor binding - 0.7995 79.95%
Androgen receptor binding - 0.5503 55.03%
Thyroid receptor binding - 0.7453 74.53%
Glucocorticoid receptor binding + 0.6536 65.36%
Aromatase binding - 0.6385 63.85%
PPAR gamma - 0.7894 78.94%
Honey bee toxicity - 0.9181 91.81%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9870 98.70%

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 97.93% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.86% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.89% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 91.65% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.01% 100.00%
CHEMBL2581 P07339 Cathepsin D 88.03% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.70% 97.09%
CHEMBL233 P35372 Mu opioid receptor 83.17% 97.93%
CHEMBL1871 P10275 Androgen Receptor 81.63% 96.43%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.54% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.37% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.03% 92.62%

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.
Rosa rugosa

Cross-Links

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PubChem 162843182
LOTUS LTS0168791
wikiData Q104918796