2-Cyclohex-3-en-1-yl-6-methylhept-5-en-2-ol

Details

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Internal ID 610905b8-1b30-44f7-86aa-bae3b01c46bc
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 2-cyclohex-3-en-1-yl-6-methylhept-5-en-2-ol
SMILES (Canonical) CC(=CCCC(C)(C1CCC=CC1)O)C
SMILES (Isomeric) CC(=CCCC(C)(C1CCC=CC1)O)C
InChI InChI=1S/C14H24O/c1-12(2)8-7-11-14(3,15)13-9-5-4-6-10-13/h4-5,8,13,15H,6-7,9-11H2,1-3H3
InChI Key NHPAJUWVDYHROB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H24O
Molecular Weight 208.34 g/mol
Exact Mass 208.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Cyclohex-3-en-1-yl-6-methylhept-5-en-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.8421 84.21%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.4275 42.75%
OATP2B1 inhibitior - 0.8503 85.03%
OATP1B1 inhibitior + 0.9198 91.98%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7076 70.76%
P-glycoprotein inhibitior - 0.9635 96.35%
P-glycoprotein substrate - 0.8898 88.98%
CYP3A4 substrate - 0.5459 54.59%
CYP2C9 substrate - 0.7759 77.59%
CYP2D6 substrate - 0.7764 77.64%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.7372 73.72%
CYP2C19 inhibition - 0.7863 78.63%
CYP2D6 inhibition - 0.9329 93.29%
CYP1A2 inhibition - 0.7807 78.07%
CYP2C8 inhibition - 0.8260 82.60%
CYP inhibitory promiscuity - 0.7213 72.13%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.6310 63.10%
Eye corrosion - 0.9199 91.99%
Eye irritation - 0.5360 53.60%
Skin irritation + 0.6357 63.57%
Skin corrosion - 0.9768 97.68%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5432 54.32%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5843 58.43%
skin sensitisation + 0.9229 92.29%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.5833 58.33%
Acute Oral Toxicity (c) III 0.8480 84.80%
Estrogen receptor binding - 0.8736 87.36%
Androgen receptor binding - 0.8868 88.68%
Thyroid receptor binding - 0.6096 60.96%
Glucocorticoid receptor binding - 0.7085 70.85%
Aromatase binding - 0.8668 86.68%
PPAR gamma - 0.5470 54.70%
Honey bee toxicity - 0.8713 87.13%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9536 95.36%

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 97.29% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.20% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.35% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.67% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.42% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.29% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.28% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 82.11% 94.73%

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 koidzumii
Rosa rugosa

Cross-Links

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PubChem 9990645
LOTUS LTS0002367
wikiData Q105179526