Ethyl 2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetate

Details

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Internal ID 2098b6f6-534a-4e51-b644-3121e32c492c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name ethyl 2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetate
SMILES (Canonical) CCOC(=O)CC1(C=CC(=O)C=C1)O
SMILES (Isomeric) CCOC(=O)CC1(C=CC(=O)C=C1)O
InChI InChI=1S/C10H12O4/c1-2-14-9(12)7-10(13)5-3-8(11)4-6-10/h3-6,13H,2,7H2,1H3
InChI Key PCTPJULDTWCNKF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O4
Molecular Weight 196.20 g/mol
Exact Mass 196.07355886 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.37
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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ethyl(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetate
ethyl 2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetate
Ethyl (1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetate
JP-2
NSC658398
NSC289072
2,5-Cyclohexadiene-1-acetic acid, 1-hydroxy-4-oxo-, ethyl ester
CHEMBL486395
SCHEMBL10249875
DTXSID40209015
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl 2-(1-hydroxy-4-oxocyclohexa-2,5-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 + 0.9863 98.63%
Caco-2 + 0.8252 82.52%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8725 87.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9398 93.98%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8159 81.59%
P-glycoprotein inhibitior - 0.9868 98.68%
P-glycoprotein substrate - 0.9727 97.27%
CYP3A4 substrate - 0.5379 53.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8937 89.37%
CYP3A4 inhibition - 0.8167 81.67%
CYP2C9 inhibition - 0.8940 89.40%
CYP2C19 inhibition - 0.8249 82.49%
CYP2D6 inhibition - 0.9296 92.96%
CYP1A2 inhibition - 0.9314 93.14%
CYP2C8 inhibition - 0.9183 91.83%
CYP inhibitory promiscuity - 0.9523 95.23%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7413 74.13%
Carcinogenicity (trinary) Non-required 0.6213 62.13%
Eye corrosion - 0.9493 94.93%
Eye irritation + 0.9876 98.76%
Skin irritation - 0.6855 68.55%
Skin corrosion - 0.9369 93.69%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8431 84.31%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5862 58.62%
skin sensitisation - 0.5296 52.96%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4548 45.48%
Acute Oral Toxicity (c) III 0.7655 76.55%
Estrogen receptor binding - 0.7073 70.73%
Androgen receptor binding - 0.8389 83.89%
Thyroid receptor binding - 0.8694 86.94%
Glucocorticoid receptor binding - 0.8030 80.30%
Aromatase binding - 0.5949 59.49%
PPAR gamma - 0.7274 72.74%
Honey bee toxicity - 0.9428 94.28%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5250 52.50%
Fish aquatic toxicity + 0.8692 86.92%

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 92.23% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.09% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.59% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.23% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 84.49% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 81.57% 94.73%

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.
Jacobaea cannabifolia
Senecio abrotanifolius

Cross-Links

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PubChem 100323
LOTUS LTS0161216
wikiData Q72475300