5-Methyl-1-(4-methylcyclohex-3-en-1-yl)hex-4-en-1-ol

Details

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Internal ID a944ff87-26db-4192-8465-563e4982c1fd
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 5-methyl-1-(4-methylcyclohex-3-en-1-yl)hex-4-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H24O/c1-11(2)5-4-6-14(15)13-9-7-12(3)8-10-13/h5,7,13-15H,4,6,8-10H2,1-3H3
InChI Key GRWNCQTXRVSTRT-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 3.60
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 5-Methyl-1-(4-methylcyclohex-3-en-1-yl)hex-4-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 + 0.9943 99.43%
Caco-2 + 0.8452 84.52%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4585 45.85%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.9452 94.52%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8661 86.61%
P-glycoprotein inhibitior - 0.9697 96.97%
P-glycoprotein substrate - 0.8218 82.18%
CYP3A4 substrate - 0.5428 54.28%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.8252 82.52%
CYP2C9 inhibition - 0.8474 84.74%
CYP2C19 inhibition - 0.8568 85.68%
CYP2D6 inhibition - 0.9240 92.40%
CYP1A2 inhibition - 0.7373 73.73%
CYP2C8 inhibition - 0.9278 92.78%
CYP inhibitory promiscuity - 0.7127 71.27%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7728 77.28%
Carcinogenicity (trinary) Non-required 0.6658 66.58%
Eye corrosion - 0.8510 85.10%
Eye irritation + 0.7002 70.02%
Skin irritation + 0.6093 60.93%
Skin corrosion - 0.9633 96.33%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5147 51.47%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.9270 92.70%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6227 62.27%
Acute Oral Toxicity (c) III 0.8046 80.46%
Estrogen receptor binding - 0.9233 92.33%
Androgen receptor binding - 0.6255 62.55%
Thyroid receptor binding - 0.7260 72.60%
Glucocorticoid receptor binding - 0.6938 69.38%
Aromatase binding - 0.8654 86.54%
PPAR gamma - 0.5573 55.73%
Honey bee toxicity - 0.9149 91.49%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9573 95.73%

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 93.51% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.05% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.52% 98.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.37% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.18% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.45% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 83.05% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.50% 95.89%

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.
Bazzania tridens

Cross-Links

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PubChem 134548342
LOTUS LTS0130332
wikiData Q105016772