8-(Methylsulfanyl)octanal oxime

Details

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Internal ID 154aae5f-deb8-4a2c-924a-0c19b6217fc8
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Oximes > Aldoximes
IUPAC Name N-(8-methylsulfanyloctylidene)hydroxylamine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H19NOS/c1-12-9-7-5-3-2-4-6-8-10-11/h8,11H,2-7,9H2,1H3
InChI Key XKNUDVRSFJJTNT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H19NOS
Molecular Weight 189.32 g/mol
Exact Mass 189.11873540 g/mol
Topological Polar Surface Area (TPSA) 57.90 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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8-(methylthio)octanaldoxime
8-methylsulfanyloctanaldoxime
8-methylsulfanyloctanal oxime
8-(methylsulfanyl)octanaldoxime
CHEBI:50703
N-[8-(methylsulfanyl)octylidene]hydroxylamine

2D Structure

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2D Structure of 8-(Methylsulfanyl)octanal oxime

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8910 89.10%
Caco-2 + 0.7617 76.17%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Lysosomes 0.5115 51.15%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9364 93.64%
OATP1B3 inhibitior + 0.9373 93.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.8776 87.76%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9311 93.11%
CYP3A4 substrate - 0.6333 63.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7836 78.36%
CYP3A4 inhibition - 0.9027 90.27%
CYP2C9 inhibition - 0.8160 81.60%
CYP2C19 inhibition - 0.7656 76.56%
CYP2D6 inhibition - 0.8426 84.26%
CYP1A2 inhibition - 0.7527 75.27%
CYP2C8 inhibition - 0.9062 90.62%
CYP inhibitory promiscuity - 0.9276 92.76%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) + 0.5295 52.95%
Carcinogenicity (trinary) Non-required 0.5589 55.89%
Eye corrosion - 0.6771 67.71%
Eye irritation + 0.8097 80.97%
Skin irritation - 0.6583 65.83%
Skin corrosion - 0.8102 81.02%
Ames mutagenesis - 0.7954 79.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5387 53.87%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation + 0.5851 58.51%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.8233 82.33%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6586 65.86%
Acute Oral Toxicity (c) III 0.6984 69.84%
Estrogen receptor binding - 0.8533 85.33%
Androgen receptor binding - 0.8944 89.44%
Thyroid receptor binding - 0.5628 56.28%
Glucocorticoid receptor binding - 0.8495 84.95%
Aromatase binding - 0.8556 85.56%
PPAR gamma - 0.6698 66.98%
Honey bee toxicity - 0.9453 94.53%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6124 61.24%
Fish aquatic toxicity + 0.6485 64.85%

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+] 89.37% 83.57%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.35% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.04% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.31% 87.45%
CHEMBL2581 P07339 Cathepsin D 85.77% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 83.73% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.03% 91.11%

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 74388157
LOTUS LTS0119860
wikiData Q27122192