3-Pentenenitrile

Details

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Internal ID 23021043-6499-44ac-ba40-3ef72a0b4454
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Organic cyanides > Nitriles
IUPAC Name (E)-pent-3-enenitrile
SMILES (Canonical) CC=CCC#N
SMILES (Isomeric) C/C=C/CC#N
InChI InChI=1S/C5H7N/c1-2-3-4-5-6/h2-3H,4H2,1H3/b3-2+
InChI Key UVKXJAUUKPDDNW-NSCUHMNNSA-N
Popularity 44 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7N
Molecular Weight 81.12 g/mol
Exact Mass 81.057849228 g/mol
Topological Polar Surface Area (TPSA) 23.80 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.48
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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4635-87-4
pent-3-enenitrile
16529-66-1
(E)-pent-3-enenitrile
(E)-3-Pentenenitrile
3-Pentenenitrile, (3E)-
Trans-3-pentenenitrile
3-Pentenonitrile
trans-3-pentenonitrile
trans-2-Butenyl cyanide
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Pentenenitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.7548 75.48%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5808 58.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8754 87.54%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8230 82.30%
P-glycoprotein inhibitior - 0.9866 98.66%
P-glycoprotein substrate - 0.9804 98.04%
CYP3A4 substrate - 0.7112 71.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7497 74.97%
CYP3A4 inhibition - 0.9438 94.38%
CYP2C9 inhibition - 0.8858 88.58%
CYP2C19 inhibition - 0.8759 87.59%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.6271 62.71%
CYP2C8 inhibition - 0.9837 98.37%
CYP inhibitory promiscuity - 0.7243 72.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.7095 70.95%
Eye corrosion + 0.9822 98.22%
Eye irritation + 0.9854 98.54%
Skin irritation + 0.8693 86.93%
Skin corrosion + 0.9362 93.62%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7128 71.28%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.7053 70.53%
skin sensitisation + 0.8223 82.23%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.6627 66.27%
Acute Oral Toxicity (c) II 0.5151 51.51%
Estrogen receptor binding - 0.9128 91.28%
Androgen receptor binding - 0.9343 93.43%
Thyroid receptor binding - 0.8864 88.64%
Glucocorticoid receptor binding - 0.7617 76.17%
Aromatase binding - 0.8929 89.29%
PPAR gamma - 0.7851 78.51%
Honey bee toxicity - 0.6248 62.48%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.4241 42.41%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1963 P16473 Thyroid stimulating hormone receptor 39810.7 nM
39810.7 nM
Potency
Potency
via CMAUP
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2039 P27338 Monoamine oxidase B 94.31% 92.51%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.75% 96.09%
CHEMBL1871 P10275 Androgen Receptor 82.16% 96.43%

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.
Brassica juncea
Sinapis alba

Cross-Links

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PubChem 5324707
NPASS NPC179860
ChEMBL CHEMBL1322495