2-Hydroxy-3-chloropenta-2,4-dienoate

Details

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Internal ID 59b3a879-af77-4b0c-848c-44bf26452e5f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Halogenated fatty acids
IUPAC Name (2Z)-3-chloro-2-hydroxypenta-2,4-dienoic acid
SMILES (Canonical) C=CC(=C(C(=O)O)O)Cl
SMILES (Isomeric) C=C/C(=C(\C(=O)O)/O)/Cl
InChI InChI=1S/C5H5ClO3/c1-2-3(6)4(7)5(8)9/h2,7H,1H2,(H,8,9)/b4-3-
InChI Key XZOBUTBZRFDQBU-ARJAWSKDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H5ClO3
Molecular Weight 148.54 g/mol
Exact Mass 147.9927217 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.27
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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(2Z)-3-chloro-2-hydroxypenta-2,4-dienoic acid
CHEBI:1121
Q27105405

2D Structure

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2D Structure of 2-Hydroxy-3-chloropenta-2,4-dienoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9778 97.78%
Caco-2 - 0.6391 63.91%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7521 75.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9356 93.56%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9614 96.14%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9927 99.27%
CYP3A4 substrate - 0.6878 68.78%
CYP2C9 substrate + 0.5915 59.15%
CYP2D6 substrate - 0.8942 89.42%
CYP3A4 inhibition - 0.8711 87.11%
CYP2C9 inhibition - 0.8167 81.67%
CYP2C19 inhibition - 0.8409 84.09%
CYP2D6 inhibition - 0.9251 92.51%
CYP1A2 inhibition - 0.8097 80.97%
CYP2C8 inhibition - 0.9561 95.61%
CYP inhibitory promiscuity - 0.9553 95.53%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.6022 60.22%
Carcinogenicity (trinary) Non-required 0.6474 64.74%
Eye corrosion + 0.8168 81.68%
Eye irritation + 0.9761 97.61%
Skin irritation + 0.7445 74.45%
Skin corrosion + 0.7165 71.65%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8380 83.80%
Micronuclear - 0.7326 73.26%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.6704 67.04%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.7746 77.46%
Acute Oral Toxicity (c) III 0.4779 47.79%
Estrogen receptor binding - 0.8456 84.56%
Androgen receptor binding - 0.8194 81.94%
Thyroid receptor binding - 0.6801 68.01%
Glucocorticoid receptor binding - 0.7740 77.40%
Aromatase binding - 0.8481 84.81%
PPAR gamma - 0.6266 62.66%
Honey bee toxicity - 0.7119 71.19%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9033 90.33%

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
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 92.80% 82.05%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 85.61% 98.51%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.11% 96.95%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 83.26% 97.34%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 83.20% 92.29%
CHEMBL4040 P28482 MAP kinase ERK2 81.71% 83.82%
CHEMBL340 P08684 Cytochrome P450 3A4 81.35% 91.19%

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 5281907
LOTUS LTS0111013
wikiData Q27105405