(4E)-1-methyl-4-(6-methylhept-6-en-2-ylidene)cyclohexene

Details

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Internal ID 769340e6-eb30-4fc4-978f-547fedcafbe5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4E)-1-methyl-4-(6-methylhept-6-en-2-ylidene)cyclohexene
SMILES (Canonical) CC1=CCC(=C(C)CCCC(=C)C)CC1
SMILES (Isomeric) CC1=CC/C(=C(\C)/CCCC(=C)C)/CC1
InChI InChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h8H,1,5-7,9-11H2,2-4H3/b15-14-
InChI Key AAQGKZZPNFGAFB-PFONDFGASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 5.18
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 (4E)-1-methyl-4-(6-methylhept-6-en-2-ylidene)cyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.9524 95.24%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.4990 49.90%
OATP2B1 inhibitior - 0.8519 85.19%
OATP1B1 inhibitior + 0.9298 92.98%
OATP1B3 inhibitior + 0.9083 90.83%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6926 69.26%
P-glycoprotein inhibitior - 0.9344 93.44%
P-glycoprotein substrate - 0.8680 86.80%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.8810 88.10%
CYP2C9 inhibition - 0.9010 90.10%
CYP2C19 inhibition - 0.8686 86.86%
CYP2D6 inhibition - 0.9347 93.47%
CYP1A2 inhibition - 0.7084 70.84%
CYP2C8 inhibition - 0.8942 89.42%
CYP inhibitory promiscuity - 0.6320 63.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.5199 51.99%
Eye corrosion + 0.6028 60.28%
Eye irritation + 0.9594 95.94%
Skin irritation + 0.7387 73.87%
Skin corrosion - 0.9787 97.87%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4662 46.62%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation + 0.9238 92.38%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.4910 49.10%
Acute Oral Toxicity (c) III 0.9373 93.73%
Estrogen receptor binding - 0.9479 94.79%
Androgen receptor binding - 0.5931 59.31%
Thyroid receptor binding - 0.7962 79.62%
Glucocorticoid receptor binding - 0.7110 71.10%
Aromatase binding - 0.7828 78.28%
PPAR gamma - 0.6086 60.86%
Honey bee toxicity - 0.9526 95.26%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL2581 P07339 Cathepsin D 94.15% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.45% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.85% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 88.29% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.42% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.28% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.09% 95.56%

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.
Cupressus macrocarpa

Cross-Links

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PubChem 11458379
LOTUS LTS0086385
wikiData Q104908283