Butanenitrile, 4-(methylthio)-

Details

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Internal ID cbf8361a-c5ff-46a4-bb7f-6f863c132c92
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Organic cyanides > Nitriles
IUPAC Name 4-methylsulfanylbutanenitrile
SMILES (Canonical) CSCCCC#N
SMILES (Isomeric) CSCCCC#N
InChI InChI=1S/C5H9NS/c1-7-5-3-2-4-6/h2-3,5H2,1H3
InChI Key JPWPMBYFDCHLKL-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NS
Molecular Weight 115.20 g/mol
Exact Mass 115.04557046 g/mol
Topological Polar Surface Area (TPSA) 49.10 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.65
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Butanenitrile, 4-(methylthio)-
4-(Methylthio)butylnitrile
4-methylsulfanylbutanenitrile
4-(Methylsulfanyl)butanenitrile
4-(methylthio)butanenitrile
4-Methylthiobutanenitrile
4-(Methylthio)butyronitrile
Butanenitrile, 4-methylthio-
4-Methylthiobutyl nitrile
3-methylthiopropyl cyanide
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Butanenitrile, 4-(methylthio)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9824 98.24%
Caco-2 + 0.8229 82.29%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.7013 70.13%
OATP2B1 inhibitior - 0.8636 86.36%
OATP1B1 inhibitior + 0.9423 94.23%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9388 93.88%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9366 93.66%
CYP3A4 substrate - 0.6221 62.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7268 72.68%
CYP3A4 inhibition - 0.9783 97.83%
CYP2C9 inhibition - 0.9224 92.24%
CYP2C19 inhibition - 0.8909 89.09%
CYP2D6 inhibition - 0.9107 91.07%
CYP1A2 inhibition - 0.6986 69.86%
CYP2C8 inhibition - 0.9676 96.76%
CYP inhibitory promiscuity - 0.9201 92.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.7421 74.21%
Eye corrosion + 0.9573 95.73%
Eye irritation + 0.9491 94.91%
Skin irritation + 0.8018 80.18%
Skin corrosion + 0.5708 57.08%
Ames mutagenesis - 0.6878 68.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7312 73.12%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5551 55.51%
skin sensitisation + 0.6297 62.97%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.7368 73.68%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6515 65.15%
Acute Oral Toxicity (c) III 0.5651 56.51%
Estrogen receptor binding - 0.8459 84.59%
Androgen receptor binding - 0.9387 93.87%
Thyroid receptor binding - 0.7119 71.19%
Glucocorticoid receptor binding - 0.7794 77.94%
Aromatase binding - 0.8092 80.92%
PPAR gamma - 0.8632 86.32%
Honey bee toxicity - 0.5567 55.67%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.6770 67.70%

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
CHEMBL226 P30542 Adenosine A1 receptor 91.12% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.14% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.46% 98.95%
CHEMBL1978 P11511 Cytochrome P450 19A1 80.03% 91.76%

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.
Brassica juncea
Brassica oleracea
Sinapis alba

Cross-Links

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PubChem 100962
NPASS NPC287350
LOTUS LTS0226494
wikiData Q83081865