7-[(S)-methylsulfinyl]heptanenitrile

Details

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Internal ID 76a6cfed-b175-4562-8302-8e909e7319b4
Taxonomy Organosulfur compounds > Sulfoxides
IUPAC Name 7-[(S)-methylsulfinyl]heptanenitrile
SMILES (Canonical) CS(=O)CCCCCCC#N
SMILES (Isomeric) C[S@](=O)CCCCCCC#N
InChI InChI=1S/C8H15NOS/c1-11(10)8-6-4-2-3-5-7-9/h2-6,8H2,1H3/t11-/m0/s1
InChI Key MVGLREOVTAENKK-NSHDSACASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H15NOS
Molecular Weight 173.28 g/mol
Exact Mass 173.08743528 g/mol
Topological Polar Surface Area (TPSA) 60.10 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-[(S)-methylsulfinyl]heptanenitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9765 97.65%
Caco-2 + 0.8287 82.87%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5412 54.12%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9479 94.79%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9132 91.32%
P-glycoprotein inhibitior - 0.9769 97.69%
P-glycoprotein substrate - 0.9366 93.66%
CYP3A4 substrate - 0.5749 57.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7453 74.53%
CYP3A4 inhibition - 0.9166 91.66%
CYP2C9 inhibition - 0.8431 84.31%
CYP2C19 inhibition - 0.7803 78.03%
CYP2D6 inhibition - 0.9115 91.15%
CYP1A2 inhibition - 0.7154 71.54%
CYP2C8 inhibition - 0.9588 95.88%
CYP inhibitory promiscuity - 0.9114 91.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5278 52.78%
Carcinogenicity (trinary) Non-required 0.7218 72.18%
Eye corrosion + 0.4859 48.59%
Eye irritation + 0.9580 95.80%
Skin irritation - 0.6223 62.23%
Skin corrosion - 0.7277 72.77%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6813 68.13%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5263 52.63%
skin sensitisation - 0.6688 66.88%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6862 68.62%
Acute Oral Toxicity (c) III 0.5314 53.14%
Estrogen receptor binding - 0.9032 90.32%
Androgen receptor binding - 0.8847 88.47%
Thyroid receptor binding - 0.7878 78.78%
Glucocorticoid receptor binding - 0.8570 85.70%
Aromatase binding - 0.8402 84.02%
PPAR gamma - 0.8485 84.85%
Honey bee toxicity - 0.5372 53.72%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.5612 56.12%

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 92.45% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.44% 98.95%
CHEMBL1978 P11511 Cytochrome P450 19A1 86.77% 91.76%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.01% 96.95%
CHEMBL1871 P10275 Androgen Receptor 83.42% 96.43%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.98% 95.17%
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.
Diptychocarpus strictus

Cross-Links

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PubChem 162876921
LOTUS LTS0053417
wikiData Q105172988