(4-Hydroxy-2-methyl-3,6-dioxo-5-pentadec-10-enylcyclohexa-1,4-dien-1-yl) acetate

Details

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Internal ID fa6ab573-2cbb-476a-a773-59611ef14671
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Benzoquinones > P-benzoquinones
IUPAC Name (4-hydroxy-2-methyl-3,6-dioxo-5-pentadec-10-enylcyclohexa-1,4-dien-1-yl) acetate
SMILES (Canonical) CCCCC=CCCCCCCCCCC1=C(C(=O)C(=C(C1=O)OC(=O)C)C)O
SMILES (Isomeric) CCCCC=CCCCCCCCCCC1=C(C(=O)C(=C(C1=O)OC(=O)C)C)O
InChI InChI=1S/C24H36O5/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-22(27)21(26)18(2)24(23(20)28)29-19(3)25/h7-8,27H,4-6,9-17H2,1-3H3
InChI Key BOVJTTALUCKCDD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H36O5
Molecular Weight 404.50 g/mol
Exact Mass 404.25627424 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 7.10
Atomic LogP (AlogP) 6.04
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 14

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-pentadec-10-enylcyclohexa-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 + 0.9802 98.02%
Caco-2 + 0.5449 54.49%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8695 86.95%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8354 83.54%
OATP1B3 inhibitior + 0.9300 93.00%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8042 80.42%
P-glycoprotein inhibitior - 0.4635 46.35%
P-glycoprotein substrate - 0.8053 80.53%
CYP3A4 substrate + 0.5348 53.48%
CYP2C9 substrate - 0.6017 60.17%
CYP2D6 substrate - 0.8880 88.80%
CYP3A4 inhibition - 0.7152 71.52%
CYP2C9 inhibition - 0.8195 81.95%
CYP2C19 inhibition - 0.6237 62.37%
CYP2D6 inhibition - 0.7213 72.13%
CYP1A2 inhibition - 0.8403 84.03%
CYP2C8 inhibition - 0.7013 70.13%
CYP inhibitory promiscuity - 0.8535 85.35%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.8382 83.82%
Carcinogenicity (trinary) Non-required 0.6620 66.20%
Eye corrosion - 0.9742 97.42%
Eye irritation - 0.5852 58.52%
Skin irritation - 0.6549 65.49%
Skin corrosion - 0.9634 96.34%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7448 74.48%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5408 54.08%
skin sensitisation - 0.7231 72.31%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5170 51.70%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.7227 72.27%
Acute Oral Toxicity (c) III 0.4736 47.36%
Estrogen receptor binding + 0.5894 58.94%
Androgen receptor binding + 0.6106 61.06%
Thyroid receptor binding - 0.6628 66.28%
Glucocorticoid receptor binding + 0.6474 64.74%
Aromatase binding - 0.5945 59.45%
PPAR gamma + 0.7127 71.27%
Honey bee toxicity - 0.9431 94.31%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7362 73.62%
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 98.79% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.81% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.17% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 92.18% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.65% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 90.65% 89.63%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.89% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.48% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.44% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.18% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.23% 96.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.36% 92.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.16% 89.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.89% 92.68%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.08% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.97% 96.00%

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 162848458
LOTUS LTS0230495
wikiData Q104940770