Pentenenitrile

Details

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Internal ID 11432a67-0c2d-4538-8e19-f8ec9ee5f558
IUPAC Name pent-2-enenitrile
SMILES (Canonical) CCC=CC#N
SMILES (Isomeric) CCC=CC#N
InChI InChI=1S/C5H7N/c1-2-3-4-5-6/h3-4H,2H2,1H3
InChI Key ISBHMJZRKAFTGE-UHFFFAOYSA-N
Popularity 9 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 1.20
Atomic LogP (AlogP) 1.48
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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DSSTox_CID_5850
DSSTox_RID_77946
DSSTox_GSID_25850
CHEMBL3185046
DTXSID6027894
ISBHMJZRKAFTGE-UHFFFAOYSA-N
Tox21_200185
NCGC00257739-01
CAS-13284-42-9
FT-0694345
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pentenenitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8366 83.66%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4574 45.74%
OATP2B1 inhibitior - 0.8725 87.25%
OATP1B1 inhibitior + 0.9104 91.04%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8224 82.24%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.9792 97.92%
CYP3A4 substrate - 0.7253 72.53%
CYP2C9 substrate - 0.6095 60.95%
CYP2D6 substrate - 0.7784 77.84%
CYP3A4 inhibition - 0.9462 94.62%
CYP2C9 inhibition - 0.8400 84.00%
CYP2C19 inhibition - 0.8791 87.91%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.6403 64.03%
CYP2C8 inhibition - 0.9746 97.46%
CYP inhibitory promiscuity - 0.5674 56.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6020 60.20%
Eye corrosion + 0.9913 99.13%
Eye irritation + 0.9850 98.50%
Skin irritation + 0.8320 83.20%
Skin corrosion + 0.8247 82.47%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7320 73.20%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.6699 66.99%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.4604 46.04%
Acute Oral Toxicity (c) III 0.6110 61.10%
Estrogen receptor binding - 0.9094 90.94%
Androgen receptor binding - 0.9348 93.48%
Thyroid receptor binding - 0.8733 87.33%
Glucocorticoid receptor binding - 0.7825 78.25%
Aromatase binding - 0.8236 82.36%
PPAR gamma - 0.8364 83.64%
Honey bee toxicity - 0.7304 73.04%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.4399 43.99%

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
CHEMBL221 P23219 Cyclooxygenase-1 87.99% 90.17%
CHEMBL1871 P10275 Androgen Receptor 86.75% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.78% 96.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 84.40% 95.58%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.20% 89.34%
CHEMBL226 P30542 Adenosine A1 receptor 80.45% 95.93%
CHEMBL230 P35354 Cyclooxygenase-2 80.14% 89.63%

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.
Elsholtzia ciliata
Mosla chinensis

Cross-Links

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PubChem 25833
NPASS NPC51067