2-Chloroacrylic acid

Details

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Internal ID 7da2001e-d49e-45b1-b05a-6c18dadeb3cc
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Alpha-halocarboxylic acids and derivatives > Alpha-halocarboxylic acids
IUPAC Name 2-chloroprop-2-enoic acid
SMILES (Canonical) C=C(C(=O)O)Cl
SMILES (Isomeric) C=C(C(=O)O)Cl
InChI InChI=1S/C3H3ClO2/c1-2(4)3(5)6/h1H2,(H,5,6)
InChI Key SZTBMYHIYNGYIA-UHFFFAOYSA-N
Popularity 48 references in papers

Physical and Chemical Properties

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Molecular Formula C3H3ClO2
Molecular Weight 106.51 g/mol
Exact Mass 105.9821570 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.82
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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598-79-8
2-chloroprop-2-enoic acid
Chloroacrylic acid
2-Propenoic acid, 2-chloro-
alpha-Chloroacrylic acid
2-CHLOROACRYLICACID
Acrylic acid, 2-chloro-
2-CHLORO-2-PROPENOIC ACID
EINECS 209-953-9
NSC 97174
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Chloroacrylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.6214 62.14%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6350 63.50%
OATP2B1 inhibitior - 0.8673 86.73%
OATP1B1 inhibitior + 0.9657 96.57%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9530 95.30%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.9965 99.65%
CYP3A4 substrate - 0.7680 76.80%
CYP2C9 substrate + 0.6063 60.63%
CYP2D6 substrate - 0.8927 89.27%
CYP3A4 inhibition - 0.8641 86.41%
CYP2C9 inhibition - 0.8377 83.77%
CYP2C19 inhibition - 0.8461 84.61%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.8093 80.93%
CYP2C8 inhibition - 0.9892 98.92%
CYP inhibitory promiscuity - 0.9761 97.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7590 75.90%
Carcinogenicity (trinary) Non-required 0.6556 65.56%
Eye corrosion + 0.9952 99.52%
Eye irritation + 0.9859 98.59%
Skin irritation + 0.8800 88.00%
Skin corrosion + 0.9706 97.06%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8245 82.45%
Micronuclear - 0.8126 81.26%
Hepatotoxicity + 0.9250 92.50%
skin sensitisation + 0.6734 67.34%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.7596 75.96%
Acute Oral Toxicity (c) II 0.4372 43.72%
Estrogen receptor binding - 0.8697 86.97%
Androgen receptor binding - 0.9362 93.62%
Thyroid receptor binding - 0.8190 81.90%
Glucocorticoid receptor binding - 0.8840 88.40%
Aromatase binding - 0.8680 86.80%
PPAR gamma - 0.7307 73.07%
Honey bee toxicity - 0.7933 79.33%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9223 92.23%

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 82.42% 96.95%

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 11735
NPASS NPC233300