2-Tolylisocyanide

Details

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Internal ID e330b0dd-9ee4-4df2-ba87-611de361fcb6
Taxonomy Benzenoids > Benzene and substituted derivatives > Toluenes
IUPAC Name 1-isocyano-2-methylbenzene
SMILES (Canonical) CC1=CC=CC=C1[N+]#[C-]
SMILES (Isomeric) CC1=CC=CC=C1[N+]#[C-]
InChI InChI=1S/C8H7N/c1-7-5-3-4-6-8(7)9-2/h3-6H,1H3
InChI Key HGHZICGHCZFYNX-UHFFFAOYSA-N
Popularity 20 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) 4.40 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.55
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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10468-64-1
1-isocyano-2-methylbenzene
o-Tolyl isocyanide
2-Methylphenylisocyanide
2-TOLYLISOCYANIDE 95
Tolylisocyanid
2-Methylphenyl isocyanide
SCHEMBL265138
DTXSID60341820
BCP21429
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Tolylisocyanide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9524 95.24%
Caco-2 + 0.9562 95.62%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5454 54.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9563 95.63%
OATP1B3 inhibitior + 0.9606 96.06%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8948 89.48%
P-glycoprotein inhibitior - 0.9903 99.03%
P-glycoprotein substrate - 0.9763 97.63%
CYP3A4 substrate - 0.7065 70.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8128 81.28%
CYP3A4 inhibition - 0.9711 97.11%
CYP2C9 inhibition - 0.7853 78.53%
CYP2C19 inhibition - 0.6699 66.99%
CYP2D6 inhibition - 0.9564 95.64%
CYP1A2 inhibition + 0.6502 65.02%
CYP2C8 inhibition - 0.8690 86.90%
CYP inhibitory promiscuity - 0.6545 65.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.7065 70.65%
Eye corrosion + 0.9450 94.50%
Eye irritation + 0.9925 99.25%
Skin irritation + 0.6446 64.46%
Skin corrosion - 0.9706 97.06%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7227 72.27%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.9250 92.50%
skin sensitisation + 0.8356 83.56%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5459 54.59%
Acute Oral Toxicity (c) III 0.8920 89.20%
Estrogen receptor binding - 0.9324 93.24%
Androgen receptor binding - 0.8792 87.92%
Thyroid receptor binding - 0.8139 81.39%
Glucocorticoid receptor binding - 0.8587 85.87%
Aromatase binding - 0.8364 83.64%
PPAR gamma - 0.9235 92.35%
Honey bee toxicity - 0.9761 97.61%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.9100 91.00%
Fish aquatic toxicity + 0.8995 89.95%

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 90.72% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.50% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.50% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.84% 93.65%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.63% 91.11%

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.
Lonicera confusa
Lonicera hypoglauca
Lonicera macrantha

Cross-Links

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PubChem 575991
NPASS NPC301317