(4-Hydroxy-2-methyl-3,6-dioxo-5-tridecylcyclohexa-1,4-dien-1-yl) acetate

Details

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Internal ID 533395d6-2197-40a6-890e-14a900a23428
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Benzoquinones > P-benzoquinones
IUPAC Name (4-hydroxy-2-methyl-3,6-dioxo-5-tridecylcyclohexa-1,4-dien-1-yl) acetate
SMILES (Canonical) CCCCCCCCCCCCCC1=C(C(=O)C(=C(C1=O)OC(=O)C)C)O
SMILES (Isomeric) CCCCCCCCCCCCCC1=C(C(=O)C(=C(C1=O)OC(=O)C)C)O
InChI InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-14-15-18-20(25)19(24)16(2)22(21(18)26)27-17(3)23/h25H,4-15H2,1-3H3
InChI Key POIGXLYMKZJQSX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O5
Molecular Weight 378.50 g/mol
Exact Mass 378.24062418 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 7.00
Atomic LogP (AlogP) 5.49
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4-Hydroxy-2-methyl-3,6-dioxo-5-tridecylcyclohexa-1,4-dien-1-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9792 97.92%
Caco-2 + 0.6702 67.02%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8661 86.61%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9055 90.55%
OATP1B3 inhibitior + 0.9192 91.92%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.4646 46.46%
P-glycoprotein inhibitior - 0.6257 62.57%
P-glycoprotein substrate - 0.8118 81.18%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5904 59.04%
CYP2D6 substrate - 0.8869 88.69%
CYP3A4 inhibition - 0.6913 69.13%
CYP2C9 inhibition - 0.8266 82.66%
CYP2C19 inhibition - 0.5818 58.18%
CYP2D6 inhibition - 0.6770 67.70%
CYP1A2 inhibition - 0.8458 84.58%
CYP2C8 inhibition - 0.7863 78.63%
CYP inhibitory promiscuity - 0.8487 84.87%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.8682 86.82%
Carcinogenicity (trinary) Non-required 0.6451 64.51%
Eye corrosion - 0.9812 98.12%
Eye irritation + 0.6933 69.33%
Skin irritation - 0.6216 62.16%
Skin corrosion - 0.9678 96.78%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4404 44.04%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6099 60.99%
skin sensitisation - 0.7214 72.14%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5281 52.81%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.7969 79.69%
Acute Oral Toxicity (c) III 0.5128 51.28%
Estrogen receptor binding + 0.5569 55.69%
Androgen receptor binding + 0.6158 61.58%
Thyroid receptor binding - 0.6072 60.72%
Glucocorticoid receptor binding + 0.5399 53.99%
Aromatase binding - 0.5997 59.97%
PPAR gamma + 0.7334 73.34%
Honey bee toxicity - 0.9622 96.22%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.7955 79.55%
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 98.52% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.68% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 94.19% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 91.85% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.34% 96.09%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 91.00% 92.68%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.98% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.21% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.50% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.12% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.31% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.57% 96.95%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.32% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.22% 97.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.25% 89.00%

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.
Maesa lanceolata

Cross-Links

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PubChem 162956986
LOTUS LTS0214699
wikiData Q105212427