2-Methyl-5-(6-methylhepta-2,5-dien-2-yl)cyclohex-2-en-1-ol

Details

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Internal ID c8010c0c-d5b8-4528-aaa7-378422cb54a9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-methyl-5-(6-methylhepta-2,5-dien-2-yl)cyclohex-2-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-11(2)6-5-7-12(3)14-9-8-13(4)15(16)10-14/h6-8,14-16H,5,9-10H2,1-4H3
InChI Key JJTAPKJBNBBXRN-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) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methyl-5-(6-methylhepta-2,5-dien-2-yl)cyclohex-2-en-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 + 0.9949 99.49%
Caco-2 + 0.7947 79.47%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5801 58.01%
OATP2B1 inhibitior - 0.8591 85.91%
OATP1B1 inhibitior + 0.9408 94.08%
OATP1B3 inhibitior + 0.9598 95.98%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8199 81.99%
P-glycoprotein inhibitior - 0.9656 96.56%
P-glycoprotein substrate - 0.8611 86.11%
CYP3A4 substrate - 0.6191 61.91%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.8549 85.49%
CYP2C9 inhibition - 0.8731 87.31%
CYP2C19 inhibition - 0.7337 73.37%
CYP2D6 inhibition - 0.8759 87.59%
CYP1A2 inhibition - 0.8342 83.42%
CYP2C8 inhibition - 0.9261 92.61%
CYP inhibitory promiscuity - 0.6580 65.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6852 68.52%
Carcinogenicity (trinary) Non-required 0.7303 73.03%
Eye corrosion - 0.8181 81.81%
Eye irritation + 0.7078 70.78%
Skin irritation + 0.6722 67.22%
Skin corrosion - 0.7056 70.56%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8394 83.94%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7021 70.21%
Acute Oral Toxicity (c) III 0.7341 73.41%
Estrogen receptor binding - 0.8445 84.45%
Androgen receptor binding - 0.8566 85.66%
Thyroid receptor binding - 0.7177 71.77%
Glucocorticoid receptor binding - 0.5220 52.20%
Aromatase binding - 0.7899 78.99%
PPAR gamma + 0.6752 67.52%
Honey bee toxicity - 0.9314 93.14%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.8863 88.63%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.48% 91.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.33% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.58% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 84.34% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.11% 97.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.06% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.20% 97.25%
CHEMBL2581 P07339 Cathepsin D 80.92% 98.95%

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.
Dumortiera hirsuta

Cross-Links

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PubChem 163035842
LOTUS LTS0173155
wikiData Q105129885