Benzyl isocyanate

Details

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Internal ID f6bb0723-992a-4101-8cca-aae52e66de70
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name isocyanatomethylbenzene
SMILES (Canonical) C1=CC=C(C=C1)CN=C=O
SMILES (Isomeric) C1=CC=C(C=C1)CN=C=O
InChI InChI=1S/C8H7NO/c10-7-9-6-8-4-2-1-3-5-8/h1-5H,6H2
InChI Key YDNLNVZZTACNJX-UHFFFAOYSA-N
Popularity 114 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7NO
Molecular Weight 133.15 g/mol
Exact Mass 133.052763847 g/mol
Topological Polar Surface Area (TPSA) 29.40 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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3173-56-6
(Isocyanatomethyl)benzene
Benzylisocyanate
Isocyanatomethylbenzene
Isocyanic Acid Benzyl Ester
Benzene, (isocyanatomethyl)-
1-(isocyanatomethyl)benzene
phenylmethyl isocyanate
8I2LI357GQ
MFCD00009701
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Benzyl isocyanate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 + 0.9176 91.76%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7376 73.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9570 95.70%
OATP1B3 inhibitior + 0.9566 95.66%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9086 90.86%
P-glycoprotein inhibitior - 0.9905 99.05%
P-glycoprotein substrate - 0.9856 98.56%
CYP3A4 substrate - 0.7333 73.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6593 65.93%
CYP3A4 inhibition - 0.9486 94.86%
CYP2C9 inhibition - 0.9441 94.41%
CYP2C19 inhibition - 0.8150 81.50%
CYP2D6 inhibition - 0.8697 86.97%
CYP1A2 inhibition + 0.6445 64.45%
CYP2C8 inhibition - 0.8603 86.03%
CYP inhibitory promiscuity - 0.7554 75.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.7241 72.41%
Eye corrosion + 0.9864 98.64%
Eye irritation + 0.9766 97.66%
Skin irritation + 0.9090 90.90%
Skin corrosion + 0.9827 98.27%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8387 83.87%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.7002 70.02%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5577 55.77%
Acute Oral Toxicity (c) III 0.8081 80.81%
Estrogen receptor binding - 0.8838 88.38%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.8847 88.47%
Glucocorticoid receptor binding - 0.7930 79.30%
Aromatase binding - 0.5314 53.14%
PPAR gamma - 0.8205 82.05%
Honey bee toxicity - 0.8188 81.88%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity - 0.5491 54.91%

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
CHEMBL2581 P07339 Cathepsin D 91.87% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.56% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.83% 94.62%
CHEMBL3401 O75469 Pregnane X receptor 84.51% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 82.98% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.14% 95.50%

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.
Simicratea welwitschii

Cross-Links

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PubChem 76639
LOTUS LTS0003341
wikiData Q27270562