(E)-13-methyl-5-(2,6,6-trimethyl-3-oxocyclohex-1-enyl)pent-2-enoic acid

Details

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Internal ID 2cca0c2e-e461-4d3b-8bfc-5d512b8cd4f6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E)-3-methyl-5-(2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)pent-2-enoic acid
SMILES (Canonical) CC1=CC(=O)CC(C1CCC(=CC(=O)O)C)(C)C
SMILES (Isomeric) CC1=CC(=O)CC(C1CC/C(=C/C(=O)O)/C)(C)C
InChI InChI=1S/C15H22O3/c1-10(7-14(17)18)5-6-13-11(2)8-12(16)9-15(13,3)4/h7-8,13H,5-6,9H2,1-4H3,(H,17,18)/b10-7+
InChI Key ZFJSQMZNZSWOPM-JXMROGBWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H22O3
Molecular Weight 250.33 g/mol
Exact Mass 250.15689456 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.36
H-Bond Acceptor 2
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 (E)-13-methyl-5-(2,6,6-trimethyl-3-oxocyclohex-1-enyl)pent-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 + 0.7181 71.81%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.9023 90.23%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.8618 86.18%
OATP1B3 inhibitior + 0.8925 89.25%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.7339 73.39%
P-glycoprotein inhibitior - 0.9224 92.24%
P-glycoprotein substrate - 0.7828 78.28%
CYP3A4 substrate + 0.5375 53.75%
CYP2C9 substrate - 0.7627 76.27%
CYP2D6 substrate - 0.9143 91.43%
CYP3A4 inhibition - 0.7294 72.94%
CYP2C9 inhibition - 0.8497 84.97%
CYP2C19 inhibition - 0.8766 87.66%
CYP2D6 inhibition - 0.9012 90.12%
CYP1A2 inhibition - 0.8612 86.12%
CYP2C8 inhibition - 0.8409 84.09%
CYP inhibitory promiscuity - 0.9229 92.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8466 84.66%
Carcinogenicity (trinary) Non-required 0.6538 65.38%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8427 84.27%
Skin irritation + 0.6335 63.35%
Skin corrosion - 0.9786 97.86%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4049 40.49%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5270 52.70%
skin sensitisation + 0.7098 70.98%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5170 51.70%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6369 63.69%
Acute Oral Toxicity (c) III 0.6760 67.60%
Estrogen receptor binding - 0.6195 61.95%
Androgen receptor binding - 0.6795 67.95%
Thyroid receptor binding - 0.5971 59.71%
Glucocorticoid receptor binding - 0.4948 49.48%
Aromatase binding - 0.6036 60.36%
PPAR gamma - 0.6131 61.31%
Honey bee toxicity - 0.9326 93.26%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9942 99.42%

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 96.03% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 91.76% 83.82%
CHEMBL2581 P07339 Cathepsin D 90.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.52% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.60% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.86% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.08% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.02% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139591345
LOTUS LTS0169575
wikiData Q105374237