(E)-3-Iodoacrylic acid

Details

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Internal ID b5b51d81-5814-4e4f-9b43-3c3dc238274c
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Acrylic acids and derivatives
IUPAC Name (E)-3-iodoprop-2-enoic acid
SMILES (Canonical) C(=CI)C(=O)O
SMILES (Isomeric) C(=C/I)\C(=O)O
InChI InChI=1S/C3H3IO2/c4-2-1-3(5)6/h1-2H,(H,5,6)/b2-1+
InChI Key IBFDLVHJHUMSAC-OWOJBTEDSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C3H3IO2
Molecular Weight 197.96 g/mol
Exact Mass 197.91778 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.02
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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6372-02-7
2-propenoic acid, 3-iodo-, (2E)-
(E)-3-Iodo-2-propenoic acid
3-iodo-2E-acrylic acid
3-Iodoacrylic acid
(E)-3-iodoprop-2-enoic acid
3-iodo-2E-propenoic acid
(2E)-3-IODOPROP-2-ENOIC ACID
71815-44-6
3-Iodoacrylicacid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (E)-3-Iodoacrylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.6938 69.38%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5165 51.65%
OATP2B1 inhibitior - 0.8689 86.89%
OATP1B1 inhibitior + 0.9518 95.18%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9551 95.51%
P-glycoprotein inhibitior - 0.9896 98.96%
P-glycoprotein substrate - 0.9969 99.69%
CYP3A4 substrate - 0.8011 80.11%
CYP2C9 substrate - 0.5962 59.62%
CYP2D6 substrate - 0.8789 87.89%
CYP3A4 inhibition - 0.9105 91.05%
CYP2C9 inhibition - 0.9012 90.12%
CYP2C19 inhibition - 0.9461 94.61%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.7863 78.63%
CYP2C8 inhibition - 0.9841 98.41%
CYP inhibitory promiscuity - 0.9846 98.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7145 71.45%
Carcinogenicity (trinary) Non-required 0.6525 65.25%
Eye corrosion + 0.9910 99.10%
Eye irritation + 0.9640 96.40%
Skin irritation + 0.9383 93.83%
Skin corrosion + 0.9806 98.06%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8905 89.05%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation + 0.6454 64.54%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.7004 70.04%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5970 59.70%
Acute Oral Toxicity (c) I 0.4483 44.83%
Estrogen receptor binding - 0.9302 93.02%
Androgen receptor binding - 0.9105 91.05%
Thyroid receptor binding - 0.8733 87.33%
Glucocorticoid receptor binding - 0.8745 87.45%
Aromatase binding - 0.9162 91.62%
PPAR gamma - 0.8108 81.08%
Honey bee toxicity - 0.9254 92.54%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.7061 70.61%

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
No predicted targets yet!

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 638126
NPASS NPC219996