1-Methyl-4-(6-methylhept-5-en-2-yl)cyclohexane

Details

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Internal ID 03085e99-6515-46af-b028-f2b31cd6ab91
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-4-(6-methylhept-5-en-2-yl)cyclohexane
SMILES (Canonical) CC1CCC(CC1)C(C)CCC=C(C)C
SMILES (Isomeric) CC1CCC(CC1)C(C)CCC=C(C)C
InChI InChI=1S/C15H28/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,13-15H,5,7-11H2,1-4H3
InChI Key PLGPPVNYZMVRCY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28
Molecular Weight 208.38 g/mol
Exact Mass 208.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.20
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Methyl-4-(6-methylhept-5-en-2-yl)cyclohexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.8953 89.53%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.3565 35.65%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9266 92.66%
OATP1B3 inhibitior + 0.8986 89.86%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7272 72.72%
P-glycoprotein inhibitior - 0.9442 94.42%
P-glycoprotein substrate - 0.8945 89.45%
CYP3A4 substrate - 0.6131 61.31%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9377 93.77%
CYP2C9 inhibition - 0.8952 89.52%
CYP2C19 inhibition - 0.9033 90.33%
CYP2D6 inhibition - 0.9423 94.23%
CYP1A2 inhibition - 0.7359 73.59%
CYP2C8 inhibition - 0.9905 99.05%
CYP inhibitory promiscuity - 0.6099 60.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.5088 50.88%
Eye corrosion + 0.5218 52.18%
Eye irritation + 0.8522 85.22%
Skin irritation + 0.7772 77.72%
Skin corrosion - 0.9609 96.09%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4553 45.53%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5610 56.10%
skin sensitisation + 0.9552 95.52%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4665 46.65%
Acute Oral Toxicity (c) III 0.8619 86.19%
Estrogen receptor binding - 0.9153 91.53%
Androgen receptor binding - 0.7880 78.80%
Thyroid receptor binding - 0.7411 74.11%
Glucocorticoid receptor binding - 0.7169 71.69%
Aromatase binding - 0.6623 66.23%
PPAR gamma - 0.7292 72.92%
Honey bee toxicity - 0.9089 90.89%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.9968 99.68%

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 92.64% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.11% 96.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 89.39% 95.58%
CHEMBL2581 P07339 Cathepsin D 88.59% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 86.96% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.59% 94.45%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.82% 96.47%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.04% 99.18%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.83% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.78% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.10% 93.56%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 80.00% 97.47%

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.
Schisandra chinensis
Zingiber officinale

Cross-Links

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PubChem 5316889
NPASS NPC227948