Benzyl Thiocyanate

Details

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Internal ID 72798cab-617b-4c4f-866c-aaee08c65f68
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyl thiocyanates
IUPAC Name benzyl thiocyanate
SMILES (Canonical) C1=CC=C(C=C1)CSC#N
SMILES (Isomeric) C1=CC=C(C=C1)CSC#N
InChI InChI=1S/C8H7NS/c9-7-10-6-8-4-2-1-3-5-8/h1-5H,6H2
InChI Key ABNDFSOIUFLJAH-UHFFFAOYSA-N
Popularity 196 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7NS
Molecular Weight 149.21 g/mol
Exact Mass 149.02992040 g/mol
Topological Polar Surface Area (TPSA) 49.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.40
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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3012-37-1
Tropeolin
Thiocyanic acid, phenylmethyl ester
Solvat 14
BENZYLTHIOCYANATE
Benzylrhodonid
Thiocyanic acid, benzyl ester
alpha-Thiocyanatotoluene
Benzyl-thiocyanate
(benzylsulfanyl)carbonitrile
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 Thiocyanate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.9174 91.74%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5200 52.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9550 95.50%
OATP1B3 inhibitior + 0.9580 95.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7920 79.20%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.9609 96.09%
CYP3A4 substrate - 0.7700 77.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6818 68.18%
CYP3A4 inhibition - 0.8694 86.94%
CYP2C9 inhibition - 0.6528 65.28%
CYP2C19 inhibition + 0.5481 54.81%
CYP2D6 inhibition - 0.8638 86.38%
CYP1A2 inhibition + 0.8318 83.18%
CYP2C8 inhibition - 0.7457 74.57%
CYP inhibitory promiscuity + 0.6721 67.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5481 54.81%
Carcinogenicity (trinary) Non-required 0.7362 73.62%
Eye corrosion + 0.9926 99.26%
Eye irritation + 0.9871 98.71%
Skin irritation + 0.9049 90.49%
Skin corrosion + 0.8740 87.40%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7014 70.14%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.7251 72.51%
skin sensitisation + 0.8883 88.83%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5196 51.96%
Acute Oral Toxicity (c) II 0.7439 74.39%
Estrogen receptor binding - 0.7453 74.53%
Androgen receptor binding - 0.8451 84.51%
Thyroid receptor binding - 0.7972 79.72%
Glucocorticoid receptor binding + 0.6323 63.23%
Aromatase binding + 0.5510 55.10%
PPAR gamma - 0.5652 56.52%
Honey bee toxicity - 0.6425 64.25%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.8331 83.31%

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 92.33% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.30% 94.62%
CHEMBL2581 P07339 Cathepsin D 91.30% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 90.37% 92.51%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.34% 96.09%
CHEMBL3902 P09211 Glutathione S-transferase Pi 84.99% 93.81%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.29% 86.33%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 82.04% 95.72%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.12% 96.42%

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.
Cichorium endivia
Lepidium meyenii
Tropaeolum majus

Cross-Links

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PubChem 18170
NPASS NPC52330
LOTUS LTS0174692
wikiData Q18341008