(Z)-2-(heptadec-10-enyl)-6-methoxycyclohexa-2,5-diene-1,4-dione

Details

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Internal ID 9851bbe5-026e-4d6f-b944-06163a40669c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Benzoquinones > P-benzoquinones
IUPAC Name 2-heptadec-10-enyl-6-methoxycyclohexa-2,5-diene-1,4-dione
SMILES (Canonical) CCCCCCC=CCCCCCCCCCC1=CC(=O)C=C(C1=O)OC
SMILES (Isomeric) CCCCCCC=CCCCCCCCCCC1=CC(=O)C=C(C1=O)OC
InChI InChI=1S/C24H38O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21-19-22(25)20-23(27-2)24(21)26/h8-9,19-20H,3-7,10-18H2,1-2H3
InChI Key YYCCUFKHCNSRIA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H38O3
Molecular Weight 374.60 g/mol
Exact Mass 374.28209507 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 8.20
Atomic LogP (AlogP) 6.63
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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NCI60_004947
(Z)-2-(heptadec-10-enyl)-6-methoxycyclohexa-2,5-diene-1,4-dione

2D Structure

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2D Structure of (Z)-2-(heptadec-10-enyl)-6-methoxycyclohexa-2,5-diene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.6079 60.79%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8346 83.46%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.8316 83.16%
OATP1B3 inhibitior + 0.9727 97.27%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.8737 87.37%
P-glycoprotein inhibitior + 0.7051 70.51%
P-glycoprotein substrate - 0.7682 76.82%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.8668 86.68%
CYP3A4 inhibition - 0.9166 91.66%
CYP2C9 inhibition - 0.8863 88.63%
CYP2C19 inhibition - 0.6588 65.88%
CYP2D6 inhibition - 0.8006 80.06%
CYP1A2 inhibition - 0.6971 69.71%
CYP2C8 inhibition + 0.4765 47.65%
CYP inhibitory promiscuity - 0.7052 70.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7886 78.86%
Carcinogenicity (trinary) Non-required 0.5777 57.77%
Eye corrosion - 0.9317 93.17%
Eye irritation + 0.6062 60.62%
Skin irritation - 0.6387 63.87%
Skin corrosion - 0.9704 97.04%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8282 82.82%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.6296 62.96%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5614 56.14%
Acute Oral Toxicity (c) III 0.7098 70.98%
Estrogen receptor binding + 0.7016 70.16%
Androgen receptor binding + 0.6900 69.00%
Thyroid receptor binding - 0.5973 59.73%
Glucocorticoid receptor binding - 0.5119 51.19%
Aromatase binding - 0.6823 68.23%
PPAR gamma + 0.6067 60.67%
Honey bee toxicity - 0.9398 93.98%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.8100 81.00%
Fish aquatic toxicity + 0.9917 99.17%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.37% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.26% 92.08%
CHEMBL2581 P07339 Cathepsin D 95.10% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.19% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.12% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.21% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.43% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 89.26% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.90% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.96% 91.11%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.87% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.69% 94.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.04% 91.81%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.92% 89.34%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.21% 92.86%
CHEMBL2885 P07451 Carbonic anhydrase III 82.96% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.85% 96.09%
CHEMBL3891 P07384 Calpain 1 81.90% 93.04%
CHEMBL3401 O75469 Pregnane X receptor 80.80% 94.73%
CHEMBL1781 P11387 DNA topoisomerase I 80.39% 97.00%

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.
Iris sibirica

Cross-Links

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PubChem 124327
LOTUS LTS0228860
wikiData Q105368383