7-Methylthioheptanonitrile oxide

Details

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Internal ID 4f13e1b4-6d2f-423d-b3e3-cd6c10b21261
IUPAC Name 7-methylsulfanylheptanenitrile oxide
SMILES (Canonical) CSCCCCCCC#[N+][O-]
SMILES (Isomeric) CSCCCCCCC#[N+][O-]
InChI InChI=1S/C8H15NOS/c1-11-8-6-4-2-3-5-7-9-10/h2-6,8H2,1H3
InChI Key RFMWHKQIFOKKGC-UHFFFAOYSA-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) 56.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 3.13
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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CHEBI:136945
6-(methylthio)heptanenitrile oxide
7-(methylthio)heptanonitrile oxide
6-(methylsulfanyl)heptanonitrile oxide
7-(methylsulfanyl)heptanenitrile oxide

2D Structure

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2D Structure of 7-Methylthioheptanonitrile oxide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9307 93.07%
Caco-2 + 0.6240 62.40%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5041 50.41%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9137 91.37%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9530 95.30%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.8618 86.18%
CYP3A4 substrate - 0.5832 58.32%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8057 80.57%
CYP3A4 inhibition - 0.9649 96.49%
CYP2C9 inhibition - 0.8265 82.65%
CYP2C19 inhibition - 0.7796 77.96%
CYP2D6 inhibition - 0.9018 90.18%
CYP1A2 inhibition - 0.7096 70.96%
CYP2C8 inhibition - 0.8303 83.03%
CYP inhibitory promiscuity - 0.9198 91.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5185 51.85%
Carcinogenicity (trinary) Non-required 0.5580 55.80%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.7332 73.32%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8026 80.26%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6047 60.47%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.6533 65.33%
skin sensitisation - 0.6163 61.63%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8772 87.72%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6032 60.32%
Acute Oral Toxicity (c) III 0.5823 58.23%
Estrogen receptor binding - 0.8225 82.25%
Androgen receptor binding - 0.9149 91.49%
Thyroid receptor binding - 0.6390 63.90%
Glucocorticoid receptor binding - 0.8038 80.38%
Aromatase binding - 0.8286 82.86%
PPAR gamma - 0.7874 78.74%
Honey bee toxicity - 0.8118 81.18%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity - 0.3767 37.67%

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 88.43% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.23% 95.17%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.17% 83.57%

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.
Arabidopsis thaliana

Cross-Links

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PubChem 46173364
LOTUS LTS0024749
wikiData Q105235491