(8a-methyl-3-propan-2-yl-2,4,5,6,7,8-hexahydro-1H-azulen-6-yl)methanol

Details

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Internal ID ae9198de-7d75-4b25-8601-1fd587673ab5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (8a-methyl-3-propan-2-yl-2,4,5,6,7,8-hexahydro-1H-azulen-6-yl)methanol
SMILES (Canonical) CC(C)C1=C2CCC(CCC2(CC1)C)CO
SMILES (Isomeric) CC(C)C1=C2CCC(CCC2(CC1)C)CO
InChI InChI=1S/C15H26O/c1-11(2)13-7-9-15(3)8-6-12(10-16)4-5-14(13)15/h11-12,16H,4-10H2,1-3H3
InChI Key RVCIHQWCEFELJN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.92
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-propan-2-yl-2,4,5,6,7,8-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 + 0.9917 99.17%
Caco-2 + 0.7555 75.55%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.7730 77.30%
OATP2B1 inhibitior - 0.8456 84.56%
OATP1B1 inhibitior + 0.8976 89.76%
OATP1B3 inhibitior + 0.9093 90.93%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8666 86.66%
P-glycoprotein inhibitior - 0.9367 93.67%
P-glycoprotein substrate - 0.8861 88.61%
CYP3A4 substrate - 0.5315 53.15%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.8881 88.81%
CYP2C9 inhibition - 0.5578 55.78%
CYP2C19 inhibition - 0.6934 69.34%
CYP2D6 inhibition - 0.9032 90.32%
CYP1A2 inhibition - 0.7826 78.26%
CYP2C8 inhibition - 0.9451 94.51%
CYP inhibitory promiscuity - 0.7364 73.64%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6135 61.35%
Eye corrosion - 0.9382 93.82%
Eye irritation + 0.7933 79.33%
Skin irritation - 0.6061 60.61%
Skin corrosion - 0.9534 95.34%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5723 57.23%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5367 53.67%
skin sensitisation + 0.6578 65.78%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.5524 55.24%
Acute Oral Toxicity (c) III 0.6442 64.42%
Estrogen receptor binding - 0.8488 84.88%
Androgen receptor binding - 0.6713 67.13%
Thyroid receptor binding - 0.5534 55.34%
Glucocorticoid receptor binding - 0.6543 65.43%
Aromatase binding - 0.7194 71.94%
PPAR gamma - 0.8666 86.66%
Honey bee toxicity - 0.9036 90.36%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9808 98.08%

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 96.76% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.62% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.29% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.06% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 88.63% 95.93%
CHEMBL2581 P07339 Cathepsin D 86.88% 98.95%
CHEMBL237 P41145 Kappa opioid receptor 86.61% 98.10%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.91% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.81% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.77% 93.56%
CHEMBL2094135 Q96BI3 Gamma-secretase 81.67% 98.05%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.13% 92.62%
CHEMBL2996 Q05655 Protein kinase C delta 80.23% 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.
Ferula sinaica

Cross-Links

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PubChem 100957403
LOTUS LTS0131527
wikiData Q105245962