Cyanoacetamide

Details

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Internal ID fec531d9-4b31-4461-9922-d3289bfc692a
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Primary carboxylic acid amides
IUPAC Name 2-cyanoacetamide
SMILES (Canonical) C(C#N)C(=O)N
SMILES (Isomeric) C(C#N)C(=O)N
InChI InChI=1S/C3H4N2O/c4-2-1-3(5)6/h1H2,(H2,5,6)
InChI Key DGJMPUGMZIKDRO-UHFFFAOYSA-N
Popularity 894 references in papers

Physical and Chemical Properties

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Molecular Formula C3H4N2O
Molecular Weight 84.08 g/mol
Exact Mass 84.032362755 g/mol
Topological Polar Surface Area (TPSA) 66.90 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.61
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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107-91-5
CYANOACETAMIDE
Acetamide, 2-cyano-
Cyanacetamide
Malonamide nitrile
Malonamonitrile
Nitrilomalonamide
Cyanoiminoacetic acid
3-Nitrilo-propionamide
Propionamide, 3-nitrilo-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyanoacetamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.6654 66.54%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.4715 47.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9765 97.65%
OATP1B3 inhibitior + 0.9485 94.85%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9073 90.73%
P-glycoprotein inhibitior - 0.9824 98.24%
P-glycoprotein substrate - 0.9869 98.69%
CYP3A4 substrate - 0.7454 74.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8245 82.45%
CYP3A4 inhibition - 0.9411 94.11%
CYP2C9 inhibition - 0.9282 92.82%
CYP2C19 inhibition - 0.9240 92.40%
CYP2D6 inhibition - 0.9488 94.88%
CYP1A2 inhibition - 0.7271 72.71%
CYP2C8 inhibition - 0.9910 99.10%
CYP inhibitory promiscuity - 0.9280 92.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6829 68.29%
Eye corrosion + 0.5745 57.45%
Eye irritation + 0.9693 96.93%
Skin irritation - 0.6871 68.71%
Skin corrosion - 0.9109 91.09%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8211 82.11%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation - 0.9262 92.62%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5153 51.53%
Acute Oral Toxicity (c) III 0.4891 48.91%
Estrogen receptor binding - 0.9415 94.15%
Androgen receptor binding - 0.8851 88.51%
Thyroid receptor binding - 0.9249 92.49%
Glucocorticoid receptor binding - 0.8571 85.71%
Aromatase binding - 0.9066 90.66%
PPAR gamma - 0.8570 85.70%
Honey bee toxicity - 0.7837 78.37%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.9842 98.42%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.04% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.16% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.34% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 80.68% 90.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.38% 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.
Hypericum japonicum

Cross-Links

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PubChem 7898
NPASS NPC61558
LOTUS LTS0078751
wikiData Q1146906