m-Tolyl isocyanate

Details

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Internal ID 73d1d989-07c4-4e34-b520-b89afa0ca23a
Taxonomy Benzenoids > Benzene and substituted derivatives > Toluenes
IUPAC Name 1-isocyanato-3-methylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H7NO/c1-7-3-2-4-8(5-7)9-6-10/h2-5H,1H3
InChI Key CPPGZWWUPFWALU-UHFFFAOYSA-N
Popularity 33 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 3.50
Atomic LogP (AlogP) 1.96
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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621-29-4
1-Isocyanato-3-methylbenzene
Benzene, 1-isocyanato-3-methyl-
3-Methylphenyl isocyanate
m-Isocyanatotoluene
3-Tolyl isocyanate
m-Methylphenyl isocyanate
QR6QV3EC23
EINECS 210-676-0
AI3-28254
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of m-Tolyl isocyanate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 + 0.8616 86.16%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6071 60.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9602 96.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8859 88.59%
P-glycoprotein inhibitior - 0.9926 99.26%
P-glycoprotein substrate - 0.9703 97.03%
CYP3A4 substrate - 0.6847 68.47%
CYP2C9 substrate - 0.7957 79.57%
CYP2D6 substrate - 0.7210 72.10%
CYP3A4 inhibition - 0.9681 96.81%
CYP2C9 inhibition - 0.9696 96.96%
CYP2C19 inhibition - 0.8635 86.35%
CYP2D6 inhibition - 0.8684 86.84%
CYP1A2 inhibition + 0.5311 53.11%
CYP2C8 inhibition - 0.8882 88.82%
CYP inhibitory promiscuity - 0.8196 81.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6067 60.67%
Eye corrosion + 0.9903 99.03%
Eye irritation + 0.9897 98.97%
Skin irritation + 0.8813 88.13%
Skin corrosion + 0.9270 92.70%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7089 70.89%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.7469 74.69%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.7490 74.90%
Acute Oral Toxicity (c) III 0.9355 93.55%
Estrogen receptor binding - 0.9546 95.46%
Androgen receptor binding - 0.8585 85.85%
Thyroid receptor binding - 0.7310 73.10%
Glucocorticoid receptor binding - 0.6612 66.12%
Aromatase binding - 0.6242 62.42%
PPAR gamma - 0.8363 83.63%
Honey bee toxicity - 0.9185 91.85%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.6482 64.82%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.41% 95.56%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 92.23% 96.42%
CHEMBL2581 P07339 Cathepsin D 91.03% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.52% 94.73%
CHEMBL2535 P11166 Glucose transporter 85.95% 98.75%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.12% 93.65%
CHEMBL3568 P29475 Nitric-oxide synthase, brain 81.00% 95.46%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.47% 94.80%

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.
Syzygium aromaticum

Cross-Links

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PubChem 69303
NPASS NPC180914