Methyl 1-hydroxy-6-oxocyclohex-2-enecarboxylate

Details

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Internal ID fcba5821-6956-45c3-b977-f7c2b27761fe
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name methyl 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate
SMILES (Canonical) COC(=O)C1(C=CCCC1=O)O
SMILES (Isomeric) COC(=O)C1(C=CCCC1=O)O
InChI InChI=1S/C8H10O4/c1-12-7(10)8(11)5-3-2-4-6(8)9/h3,5,11H,2,4H2,1H3
InChI Key IJZJQOKHINBQCY-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O4
Molecular Weight 170.16 g/mol
Exact Mass 170.05790880 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.19
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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1-Hydroxy-6-oxo-2-cyclohexene-1-carboxylic acid methyl ester
DTXSID801230733
methyl 1-hydroxy-6-oxocyclohex-2-enecarboxylate
Methyl 1-hydroxy-6-oxo-2-cyclohexene-1-carboxylate

2D Structure

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2D Structure of Methyl 1-hydroxy-6-oxocyclohex-2-enecarboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8975 89.75%
Caco-2 - 0.6057 60.57%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.9191 91.91%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.9677 96.77%
OATP1B3 inhibitior + 0.9674 96.74%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9625 96.25%
P-glycoprotein inhibitior - 0.9780 97.80%
P-glycoprotein substrate - 0.9435 94.35%
CYP3A4 substrate - 0.5672 56.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8507 85.07%
CYP3A4 inhibition - 0.9343 93.43%
CYP2C9 inhibition - 0.9355 93.55%
CYP2C19 inhibition - 0.8976 89.76%
CYP2D6 inhibition - 0.9498 94.98%
CYP1A2 inhibition - 0.9145 91.45%
CYP2C8 inhibition - 0.9558 95.58%
CYP inhibitory promiscuity - 0.9885 98.85%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8083 80.83%
Carcinogenicity (trinary) Non-required 0.5957 59.57%
Eye corrosion - 0.9065 90.65%
Eye irritation + 0.9144 91.44%
Skin irritation - 0.5603 56.03%
Skin corrosion - 0.8390 83.90%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7611 76.11%
Micronuclear - 0.7341 73.41%
Hepatotoxicity + 0.5482 54.82%
skin sensitisation - 0.8284 82.84%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6458 64.58%
Acute Oral Toxicity (c) III 0.6374 63.74%
Estrogen receptor binding - 0.8386 83.86%
Androgen receptor binding - 0.7055 70.55%
Thyroid receptor binding - 0.8487 84.87%
Glucocorticoid receptor binding - 0.7480 74.80%
Aromatase binding - 0.8626 86.26%
PPAR gamma - 0.8301 83.01%
Honey bee toxicity - 0.9532 95.32%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.4324 43.24%

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 96.07% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.99% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.44% 96.09%
CHEMBL4208 P20618 Proteasome component C5 86.51% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.86% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 84.55% 83.82%
CHEMBL230 P35354 Cyclooxygenase-2 83.58% 89.63%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.23% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.46% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.95% 91.07%
CHEMBL2581 P07339 Cathepsin D 81.82% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.74% 94.00%

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.
Dovyalis abyssinica

Cross-Links

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PubChem 23649674
LOTUS LTS0062274
wikiData Q105114241