Pent-4-enamide

Details

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Internal ID 6f3dd3e3-5656-4d1f-83bb-ac8553a83fbf
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty amides
IUPAC Name pent-4-enamide
SMILES (Canonical) C=CCCC(=O)N
SMILES (Isomeric) C=CCCC(=O)N
InChI InChI=1S/C5H9NO/c1-2-3-4-5(6)7/h2H,1,3-4H2,(H2,6,7)
InChI Key DVFGVGYKHMQZJC-UHFFFAOYSA-N
Popularity 22 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 0.20
Atomic LogP (AlogP) 0.44
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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6852-94-4
4-Pentenamide
Pent-4-enoic acid amide
allylacetamide
allyl acetamide
DTXSID20473353
DVFGVGYKHMQZJC-UHFFFAOYSA-N
MFCD17015388
AKOS006239817
EN300-210701

2D Structure

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2D Structure of Pent-4-enamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.8099 80.99%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.4538 45.38%
OATP2B1 inhibitior - 0.8652 86.52%
OATP1B1 inhibitior + 0.9569 95.69%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 0.9418 94.18%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9198 91.98%
P-glycoprotein inhibitior - 0.9876 98.76%
P-glycoprotein substrate - 0.9882 98.82%
CYP3A4 substrate - 0.7441 74.41%
CYP2C9 substrate - 0.8030 80.30%
CYP2D6 substrate - 0.8293 82.93%
CYP3A4 inhibition - 0.8058 80.58%
CYP2C9 inhibition - 0.8576 85.76%
CYP2C19 inhibition - 0.8585 85.85%
CYP2D6 inhibition - 0.9116 91.16%
CYP1A2 inhibition - 0.5158 51.58%
CYP2C8 inhibition - 0.9873 98.73%
CYP inhibitory promiscuity - 0.8594 85.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.5483 54.83%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.9335 93.35%
Skin irritation - 0.6964 69.64%
Skin corrosion - 0.8847 88.47%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8267 82.67%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9389 93.89%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.5754 57.54%
Acute Oral Toxicity (c) III 0.5915 59.15%
Estrogen receptor binding - 0.9734 97.34%
Androgen receptor binding - 0.9583 95.83%
Thyroid receptor binding - 0.8979 89.79%
Glucocorticoid receptor binding - 0.9065 90.65%
Aromatase binding - 0.8817 88.17%
PPAR gamma - 0.9176 91.76%
Honey bee toxicity - 0.8544 85.44%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.9383 93.83%

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 86.72% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.70% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 84.91% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.17% 91.11%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 83.97% 82.05%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.88% 96.95%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 83.20% 98.51%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.95% 99.17%

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.
Descurainia sophia
Isatis tinctoria

Cross-Links

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PubChem 11815293
NPASS NPC194698