3-Butenyl thiocyanate

Details

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Internal ID 70f4761a-f723-46d5-8084-1e91d8d3f412
IUPAC Name but-3-enyl thiocyanate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H7NS/c1-2-3-4-7-5-6/h2H,1,3-4H2
InChI Key LTYOTHHOFKKKQH-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7NS
Molecular Weight 113.18 g/mol
Exact Mass 113.02992040 g/mol
Topological Polar Surface Area (TPSA) 49.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.78
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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SCHEMBL4814097

2D Structure

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2D Structure of 3-Butenyl thiocyanate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9750 97.50%
Caco-2 + 0.6451 64.51%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.4087 40.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9363 93.63%
OATP1B3 inhibitior + 0.9506 95.06%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9087 90.87%
P-glycoprotein inhibitior - 0.9820 98.20%
P-glycoprotein substrate - 0.9763 97.63%
CYP3A4 substrate - 0.6889 68.89%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.7046 70.46%
CYP3A4 inhibition - 0.9320 93.20%
CYP2C9 inhibition - 0.8036 80.36%
CYP2C19 inhibition - 0.7101 71.01%
CYP2D6 inhibition - 0.9024 90.24%
CYP1A2 inhibition - 0.5124 51.24%
CYP2C8 inhibition - 0.9301 93.01%
CYP inhibitory promiscuity + 0.5299 52.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5475 54.75%
Eye corrosion + 0.9847 98.47%
Eye irritation + 0.9080 90.80%
Skin irritation + 0.8050 80.50%
Skin corrosion + 0.5671 56.71%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6599 65.99%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.6549 65.49%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.8057 80.57%
Acute Oral Toxicity (c) II 0.5873 58.73%
Estrogen receptor binding - 0.8568 85.68%
Androgen receptor binding - 0.9295 92.95%
Thyroid receptor binding - 0.7709 77.09%
Glucocorticoid receptor binding - 0.6031 60.31%
Aromatase binding - 0.7052 70.52%
PPAR gamma - 0.8142 81.42%
Honey bee toxicity + 0.7737 77.37%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.6629 66.29%

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
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 85.62% 83.57%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.56% 89.34%
CHEMBL2039 P27338 Monoamine oxidase B 84.03% 92.51%
CHEMBL4040 P28482 MAP kinase ERK2 83.77% 83.82%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 81.88% 85.40%
CHEMBL1929 P47989 Xanthine dehydrogenase 81.40% 96.12%
CHEMBL240 Q12809 HERG 81.03% 89.76%
CHEMBL226 P30542 Adenosine A1 receptor 80.75% 95.93%

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.
Descurainia sophia

Cross-Links

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PubChem 11228778
LOTUS LTS0144534
wikiData Q104376060