1-Hept-6-en-2-yl-4-methylcyclohexa-1,3-diene

Details

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Internal ID 1d9ba2f0-26e4-44aa-aef9-63c160166411
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 1-hept-6-en-2-yl-4-methylcyclohexa-1,3-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22/c1-4-5-6-7-13(3)14-10-8-12(2)9-11-14/h4,8,10,13H,1,5-7,9,11H2,2-3H3
InChI Key NIOHMVMTJUYICJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22
Molecular Weight 190.32 g/mol
Exact Mass 190.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.65
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Hept-6-en-2-yl-4-methylcyclohexa-1,3-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9898 98.98%
Caco-2 + 0.9218 92.18%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Lysosomes 0.5665 56.65%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.9467 94.67%
OATP1B3 inhibitior + 0.9176 91.76%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.6986 69.86%
P-glycoprotein inhibitior - 0.9635 96.35%
P-glycoprotein substrate - 0.8609 86.09%
CYP3A4 substrate - 0.5816 58.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7650 76.50%
CYP3A4 inhibition - 0.9093 90.93%
CYP2C9 inhibition - 0.9252 92.52%
CYP2C19 inhibition - 0.8906 89.06%
CYP2D6 inhibition - 0.9308 93.08%
CYP1A2 inhibition - 0.6920 69.20%
CYP2C8 inhibition - 0.9569 95.69%
CYP inhibitory promiscuity - 0.6495 64.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Warning 0.5115 51.15%
Eye corrosion + 0.7398 73.98%
Eye irritation + 0.6248 62.48%
Skin irritation + 0.6996 69.96%
Skin corrosion - 0.9840 98.40%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3820 38.20%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.9562 95.62%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4622 46.22%
Acute Oral Toxicity (c) III 0.9378 93.78%
Estrogen receptor binding - 0.9533 95.33%
Androgen receptor binding - 0.7492 74.92%
Thyroid receptor binding - 0.6973 69.73%
Glucocorticoid receptor binding - 0.7573 75.73%
Aromatase binding - 0.8517 85.17%
PPAR gamma - 0.6599 65.99%
Honey bee toxicity - 0.9397 93.97%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5400 54.00%
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 90.91% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.64% 94.73%
CHEMBL2885 P07451 Carbonic anhydrase III 88.10% 87.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.86% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.39% 93.40%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.71% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.69% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.17% 93.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.44% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 83.21% 94.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.82% 99.17%

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.
Senecio digitalifolius

Cross-Links

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PubChem 71439785
LOTUS LTS0171782
wikiData Q105179926