trans-3-Chloroacrylic acid

Details

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Internal ID 625cc99f-626f-4602-a736-643acc3191ae
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Acrylic acids and derivatives
IUPAC Name (E)-3-chloroprop-2-enoic acid
SMILES (Canonical) C(=CCl)C(=O)O
SMILES (Isomeric) C(=C/Cl)\C(=O)O
InChI InChI=1S/C3H3ClO2/c4-2-1-3(5)6/h1-2H,(H,5,6)/b2-1+
InChI Key MHMUCYJKZUZMNJ-OWOJBTEDSA-N
Popularity 51 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 0.70
Atomic LogP (AlogP) 0.82
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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2345-61-1
(E)-3-Chloroacrylic acid
3-Chloroacrylic acid
625-40-1
trans-3-Chloropropenoic acid
2-Propenoic acid, 3-chloro-, (E)-
(E)-3-chloroprop-2-enoic acid
2-propenoic acid, 3-chloro-, (2E)-
3-chloroprop-2-enoic acid
Acrylic acid, 3-chloro-, trans-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of trans-3-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 + 0.9957 99.57%
Caco-2 + 0.6940 69.40%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5786 57.86%
OATP2B1 inhibitior - 0.8703 87.03%
OATP1B1 inhibitior + 0.9500 95.00%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9619 96.19%
P-glycoprotein inhibitior - 0.9870 98.70%
P-glycoprotein substrate - 0.9968 99.68%
CYP3A4 substrate - 0.7521 75.21%
CYP2C9 substrate + 0.5962 59.62%
CYP2D6 substrate - 0.8804 88.04%
CYP3A4 inhibition - 0.9290 92.90%
CYP2C9 inhibition - 0.8911 89.11%
CYP2C19 inhibition - 0.9112 91.12%
CYP2D6 inhibition - 0.9319 93.19%
CYP1A2 inhibition - 0.7733 77.33%
CYP2C8 inhibition - 0.9704 97.04%
CYP inhibitory promiscuity - 0.9836 98.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7445 74.45%
Carcinogenicity (trinary) Non-required 0.5732 57.32%
Eye corrosion + 0.9972 99.72%
Eye irritation + 0.9842 98.42%
Skin irritation + 0.9547 95.47%
Skin corrosion + 0.9970 99.70%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8991 89.91%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.5878 58.78%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.7303 73.03%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5926 59.26%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding - 0.9401 94.01%
Androgen receptor binding - 0.8841 88.41%
Thyroid receptor binding - 0.8549 85.49%
Glucocorticoid receptor binding - 0.8504 85.04%
Aromatase binding - 0.9199 91.99%
PPAR gamma - 0.8310 83.10%
Honey bee toxicity - 0.8595 85.95%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity + 0.7036 70.36%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.86% 89.34%

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 638124
NPASS NPC249597