2-Chloro-3-oxohexanedioic acid

Details

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Internal ID 8d5ba6a2-01fd-45fd-b5dd-de1f58d13d40
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Medium-chain keto acids and derivatives
IUPAC Name 2-chloro-3-oxohexanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H7ClO5/c7-5(6(11)12)3(8)1-2-4(9)10/h5H,1-2H2,(H,9,10)(H,11,12)
InChI Key YJYHEBUTQYISNJ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C6H7ClO5
Molecular Weight 194.57 g/mol
Exact Mass 193.9982010 g/mol
Topological Polar Surface Area (TPSA) 91.70 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.11
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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C12836
AC1L9FH7
2-chloro-3-oxoadipic acid
2-chloro-3-oxo-hexanedioic acid
CHEBI:19500

2D Structure

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2D Structure of 2-Chloro-3-oxohexanedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7511 75.11%
Caco-2 - 0.8300 83.00%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8489 84.89%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9330 93.30%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9595 95.95%
P-glycoprotein inhibitior - 0.9856 98.56%
P-glycoprotein substrate - 0.9855 98.55%
CYP3A4 substrate - 0.7280 72.80%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.8513 85.13%
CYP3A4 inhibition - 0.8955 89.55%
CYP2C9 inhibition - 0.9296 92.96%
CYP2C19 inhibition - 0.8918 89.18%
CYP2D6 inhibition - 0.9342 93.42%
CYP1A2 inhibition - 0.9054 90.54%
CYP2C8 inhibition - 0.9831 98.31%
CYP inhibitory promiscuity - 0.9802 98.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6725 67.25%
Carcinogenicity (trinary) Non-required 0.6423 64.23%
Eye corrosion + 0.6925 69.25%
Eye irritation + 0.9375 93.75%
Skin irritation - 0.6418 64.18%
Skin corrosion + 0.8774 87.74%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7541 75.41%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.6802 68.02%
skin sensitisation - 0.9192 91.92%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.5775 57.75%
Acute Oral Toxicity (c) III 0.6146 61.46%
Estrogen receptor binding - 0.8367 83.67%
Androgen receptor binding - 0.8722 87.22%
Thyroid receptor binding - 0.7194 71.94%
Glucocorticoid receptor binding - 0.6996 69.96%
Aromatase binding - 0.8832 88.32%
PPAR gamma - 0.4858 48.58%
Honey bee toxicity - 0.7998 79.98%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.9290 92.90%
Fish aquatic toxicity - 0.6328 63.28%

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
CHEMBL4040 P28482 MAP kinase ERK2 94.22% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 93.15% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.32% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.88% 99.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.43% 92.26%
CHEMBL2581 P07339 Cathepsin D 81.46% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.90% 96.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.13% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 443963
LOTUS LTS0275709
wikiData Q105349546