Angelic acid amide

Details

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Internal ID d856f80f-ed52-4952-9485-a8222b4ba82a
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Primary carboxylic acid amides
IUPAC Name (Z)-2-methylbut-2-enamide
SMILES (Canonical) CC=C(C)C(=O)N
SMILES (Isomeric) C/C=C(/C)\C(=O)N
InChI InChI=1S/C5H9NO/c1-3-4(2)5(6)7/h3H,1-2H3,(H2,6,7)/b4-3-
InChI Key KFTHUBZIEMOORC-ARJAWSKDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NO
Molecular Weight 99.13 g/mol
Exact Mass 99.068413911 g/mol
Topological Polar Surface Area (TPSA) 43.10 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.44
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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(Z)-2-methylbut-2-enamide
AKOS006342718

2D Structure

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2D Structure of Angelic acid amide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.7649 76.49%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.6230 62.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9597 95.97%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.9018 90.18%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8996 89.96%
P-glycoprotein inhibitior - 0.9879 98.79%
P-glycoprotein substrate - 0.9817 98.17%
CYP3A4 substrate - 0.7496 74.96%
CYP2C9 substrate - 0.7867 78.67%
CYP2D6 substrate - 0.9034 90.34%
CYP3A4 inhibition - 0.9549 95.49%
CYP2C9 inhibition - 0.8506 85.06%
CYP2C19 inhibition - 0.9150 91.50%
CYP2D6 inhibition - 0.8686 86.86%
CYP1A2 inhibition - 0.8030 80.30%
CYP2C8 inhibition - 0.9953 99.53%
CYP inhibitory promiscuity - 0.8903 89.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5800 58.00%
Carcinogenicity (trinary) Warning 0.3533 35.33%
Eye corrosion + 0.8302 83.02%
Eye irritation + 0.9882 98.82%
Skin irritation - 0.8050 80.50%
Skin corrosion - 0.9067 90.67%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7758 77.58%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.9386 93.86%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5905 59.05%
Acute Oral Toxicity (c) III 0.8000 80.00%
Estrogen receptor binding - 0.9610 96.10%
Androgen receptor binding - 0.8816 88.16%
Thyroid receptor binding - 0.8491 84.91%
Glucocorticoid receptor binding - 0.9243 92.43%
Aromatase binding - 0.8369 83.69%
PPAR gamma - 0.9283 92.83%
Honey bee toxicity - 0.9274 92.74%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity - 0.7864 78.64%

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 90.33% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.89% 91.11%
CHEMBL3474 P14555 Phospholipase A2 group IIA 80.76% 94.05%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.09% 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.
Delairea odorata

Cross-Links

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PubChem 5784553
LOTUS LTS0152106
wikiData Q105140551