(E)-2,3-dichloro-acrylic acid

Details

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Internal ID 97a32325-0368-43a9-bf0e-d21a9a15ba99
Taxonomy Organohalogen compounds > Vinyl halides > Vinylogous halides
IUPAC Name (E)-2,3-dichloroprop-2-enoic acid
SMILES (Canonical) C(=C(C(=O)O)Cl)Cl
SMILES (Isomeric) C(=C(\C(=O)O)/Cl)\Cl
InChI InChI=1S/C3H2Cl2O2/c4-1-2(5)3(6)7/h1H,(H,6,7)/b2-1+
InChI Key YQYHCJZVJNOGBP-OWOJBTEDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C3H2Cl2O2
Molecular Weight 140.95 g/mol
Exact Mass 139.9431847 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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(E)-2,3-dichloro-acrylic acid
SCHEMBL8907761
(E)-2,3-Dichloroacrylic acid
DTXSID601023425
(2E)-2,3-dichloro-2-propenoic acid

2D Structure

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2D Structure of (E)-2,3-dichloro-acrylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.5623 56.23%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6594 65.94%
OATP2B1 inhibitior - 0.8685 86.85%
OATP1B1 inhibitior + 0.9476 94.76%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9518 95.18%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9939 99.39%
CYP3A4 substrate - 0.7396 73.96%
CYP2C9 substrate + 0.6023 60.23%
CYP2D6 substrate - 0.8900 89.00%
CYP3A4 inhibition - 0.9368 93.68%
CYP2C9 inhibition - 0.8407 84.07%
CYP2C19 inhibition - 0.8854 88.54%
CYP2D6 inhibition - 0.9342 93.42%
CYP1A2 inhibition - 0.7863 78.63%
CYP2C8 inhibition - 0.9665 96.65%
CYP inhibitory promiscuity - 0.9723 97.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7490 74.90%
Carcinogenicity (trinary) Non-required 0.5893 58.93%
Eye corrosion + 0.9947 99.47%
Eye irritation + 0.9851 98.51%
Skin irritation + 0.9120 91.20%
Skin corrosion + 0.9895 98.95%
Ames mutagenesis + 0.5656 56.56%
Human Ether-a-go-go-Related Gene inhibition - 0.8662 86.62%
Micronuclear - 0.8026 80.26%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation + 0.6597 65.97%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8525 85.25%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6814 68.14%
Acute Oral Toxicity (c) III 0.5726 57.26%
Estrogen receptor binding - 0.8493 84.93%
Androgen receptor binding - 0.9346 93.46%
Thyroid receptor binding - 0.7586 75.86%
Glucocorticoid receptor binding - 0.8065 80.65%
Aromatase binding - 0.8274 82.74%
PPAR gamma - 0.7420 74.20%
Honey bee toxicity - 0.7435 74.35%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8332 83.32%

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
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.03% 96.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 83.95% 92.29%
CHEMBL4040 P28482 MAP kinase ERK2 81.56% 83.82%

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.
Ainsliaea dissecta
Platycarphella carlinoides
Pulicaria dysenterica
Uncaria homomalla

Cross-Links

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PubChem 24977677
NPASS NPC96441