2-Methyl-6-(4-methylphenyl)hept-2-enal

Details

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Internal ID 7fb81c60-fa55-4a8e-922a-976cbee5a04b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-methyl-6-(4-methylphenyl)hept-2-enal
SMILES (Canonical) CC1=CC=C(C=C1)C(C)CCC=C(C)C=O
SMILES (Isomeric) CC1=CC=C(C=C1)C(C)CCC=C(C)C=O
InChI InChI=1S/C15H20O/c1-12-7-9-15(10-8-12)14(3)6-4-5-13(2)11-16/h5,7-11,14H,4,6H2,1-3H3
InChI Key QCINNYOCRHJODG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O
Molecular Weight 216.32 g/mol
Exact Mass 216.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.02
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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18744-24-6
DTXSID20774498

2D Structure

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2D Structure of 2-Methyl-6-(4-methylphenyl)hept-2-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.9294 92.94%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.2801 28.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9132 91.32%
OATP1B3 inhibitior + 0.8998 89.98%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9561 95.61%
P-glycoprotein substrate - 0.8876 88.76%
CYP3A4 substrate - 0.6531 65.31%
CYP2C9 substrate - 0.5624 56.24%
CYP2D6 substrate - 0.8124 81.24%
CYP3A4 inhibition - 0.9360 93.60%
CYP2C9 inhibition - 0.9193 91.93%
CYP2C19 inhibition - 0.8431 84.31%
CYP2D6 inhibition - 0.9137 91.37%
CYP1A2 inhibition - 0.5632 56.32%
CYP2C8 inhibition - 0.9910 99.10%
CYP inhibitory promiscuity - 0.5284 52.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.5636 56.36%
Eye corrosion - 0.7038 70.38%
Eye irritation + 0.6926 69.26%
Skin irritation + 0.8829 88.29%
Skin corrosion - 0.7946 79.46%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3738 37.38%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.9554 95.54%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5725 57.25%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.4603 46.03%
Acute Oral Toxicity (c) III 0.9194 91.94%
Estrogen receptor binding - 0.7105 71.05%
Androgen receptor binding - 0.7822 78.22%
Thyroid receptor binding - 0.6707 67.07%
Glucocorticoid receptor binding - 0.7540 75.40%
Aromatase binding - 0.5395 53.95%
PPAR gamma - 0.7515 75.15%
Honey bee toxicity - 0.9393 93.93%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9815 98.15%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.40% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.08% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 92.43% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.72% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.03% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.54% 96.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.01% 90.24%

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.
Torreya nucifera

Cross-Links

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PubChem 71348610
LOTUS LTS0193316
wikiData Q82735659