Phenylacetonitrile

Details

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Internal ID bb22e988-55d4-46bf-bab6-5c9403d58de0
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyl cyanides
IUPAC Name 2-phenylacetonitrile
SMILES (Canonical) C1=CC=C(C=C1)CC#N
SMILES (Isomeric) C1=CC=C(C=C1)CC#N
InChI InChI=1S/C8H7N/c9-7-6-8-4-2-1-3-5-8/h1-5H,6H2
InChI Key SUSQOBVLVYHIEX-UHFFFAOYSA-N
Popularity 1,578 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7N
Molecular Weight 117.15 g/mol
Exact Mass 117.057849228 g/mol
Topological Polar Surface Area (TPSA) 23.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Benzeneacetonitrile
2-Phenylacetonitrile
BENZYL CYANIDE
140-29-4
alpha-Tolunitrile
Benzyl nitrile
alpha-Cyanotoluene
(Cyanomethyl)benzene
Phenyl acetyl nitrile
Benzylnitrile
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phenylacetonitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.9290 92.90%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.9143 91.43%
Subcellular localzation Lysosomes 0.4814 48.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9459 94.59%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8292 82.92%
P-glycoprotein inhibitior - 0.9876 98.76%
P-glycoprotein substrate - 0.9784 97.84%
CYP3A4 substrate - 0.7536 75.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4122 41.22%
CYP3A4 inhibition - 0.8651 86.51%
CYP2C9 inhibition - 0.8163 81.63%
CYP2C19 inhibition - 0.6810 68.10%
CYP2D6 inhibition - 0.8789 87.89%
CYP1A2 inhibition + 0.7207 72.07%
CYP2C8 inhibition - 0.8305 83.05%
CYP inhibitory promiscuity - 0.5338 53.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5581 55.81%
Carcinogenicity (trinary) Non-required 0.6886 68.86%
Eye corrosion + 0.9862 98.62%
Eye irritation + 0.9940 99.40%
Skin irritation + 0.9269 92.69%
Skin corrosion + 0.7037 70.37%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6933 69.33%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6876 68.76%
skin sensitisation + 0.9239 92.39%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5673 56.73%
Acute Oral Toxicity (c) II 0.7301 73.01%
Estrogen receptor binding - 0.8824 88.24%
Androgen receptor binding - 0.8533 85.33%
Thyroid receptor binding - 0.8424 84.24%
Glucocorticoid receptor binding - 0.7243 72.43%
Aromatase binding - 0.7369 73.69%
PPAR gamma - 0.7477 74.77%
Honey bee toxicity - 0.6564 65.64%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.6468 64.68%

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 93.65% 90.17%
CHEMBL2581 P07339 Cathepsin D 92.80% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.37% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.39% 96.09%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.53% 93.81%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.97% 95.56%

Cross-Links

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PubChem 8794
NPASS NPC50266
LOTUS LTS0082558
wikiData Q425620