Pentanenitrile, 5-(methylsulfinyl)-

Details

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Internal ID d44ba14b-8ccb-48cb-a663-eeb6cf137c4a
Taxonomy Organosulfur compounds > Sulfoxides
IUPAC Name 5-methylsulfinylpentanenitrile
SMILES (Canonical) CS(=O)CCCCC#N
SMILES (Isomeric) CS(=O)CCCCC#N
InChI InChI=1S/C6H11NOS/c1-9(8)6-4-2-3-5-7/h2-4,6H2,1H3
InChI Key FGYQUFZANKOISC-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NOS
Molecular Weight 145.23 g/mol
Exact Mass 145.05613515 g/mol
Topological Polar Surface Area (TPSA) 60.10 Ų
XlogP -0.30
Atomic LogP (AlogP) 1.06
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Sulforaphane nitrile
5-METHANESULFINYLPENTANENITRILE
5-methylsulfinylpentanenitrile
Pentanenitrile, 5-(methylsulfinyl)-
5-(Methylsulfinyl)pentanenitrile
starbld0046341
5-methylsulfinylpentyl nitrile
SCHEMBL9277702
5-(methylsulfinyl)-pentanenitrile
DTXSID50337631
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pentanenitrile, 5-(methylsulfinyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9703 97.03%
Caco-2 + 0.9099 90.99%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Lysosomes 0.5560 55.60%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9416 94.16%
OATP1B3 inhibitior + 0.9435 94.35%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9137 91.37%
P-glycoprotein inhibitior - 0.9824 98.24%
P-glycoprotein substrate - 0.9413 94.13%
CYP3A4 substrate - 0.5916 59.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7453 74.53%
CYP3A4 inhibition - 0.9040 90.40%
CYP2C9 inhibition - 0.8337 83.37%
CYP2C19 inhibition - 0.7689 76.89%
CYP2D6 inhibition - 0.9033 90.33%
CYP1A2 inhibition - 0.6943 69.43%
CYP2C8 inhibition - 0.9669 96.69%
CYP inhibitory promiscuity - 0.8991 89.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5278 52.78%
Carcinogenicity (trinary) Non-required 0.7184 71.84%
Eye corrosion + 0.4879 48.79%
Eye irritation + 0.9647 96.47%
Skin irritation - 0.6038 60.38%
Skin corrosion - 0.7320 73.20%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7538 75.38%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.5230 52.30%
skin sensitisation - 0.6889 68.89%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6849 68.49%
Acute Oral Toxicity (c) III 0.5241 52.41%
Estrogen receptor binding - 0.8895 88.95%
Androgen receptor binding - 0.8979 89.79%
Thyroid receptor binding - 0.8621 86.21%
Glucocorticoid receptor binding - 0.7648 76.48%
Aromatase binding - 0.8151 81.51%
PPAR gamma - 0.8764 87.64%
Honey bee toxicity - 0.5071 50.71%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.7369 73.69%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.26% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.37% 98.95%
CHEMBL1978 P11511 Cytochrome P450 19A1 87.26% 91.76%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.01% 96.95%
CHEMBL1871 P10275 Androgen Receptor 83.19% 96.43%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.69% 96.00%

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 oleracea

Cross-Links

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PubChem 543743
LOTUS LTS0030578
wikiData Q82105550