6-methylsulfinyl-6'-methylthio-N,N'-di-n-hexylurea

Details

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Internal ID 5a793a78-fb56-4c45-925a-3877bdb1f027
Taxonomy Organic acids and derivatives > Organic carbonic acids and derivatives > Ureas
IUPAC Name 1-(6-methylsulfanylhexyl)-3-(6-methylsulfinylhexyl)urea
SMILES (Canonical) CSCCCCCCNC(=O)NCCCCCCS(=O)C
SMILES (Isomeric) CSCCCCCCNC(=O)NCCCCCCS(=O)C
InChI InChI=1S/C15H32N2O2S2/c1-20-13-9-5-3-7-11-16-15(18)17-12-8-4-6-10-14-21(2)19/h3-14H2,1-2H3,(H2,16,17,18)
InChI Key QOIKVUAQMGLXCY-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C15H32N2O2S2
Molecular Weight 336.60 g/mol
Exact Mass 336.19052061 g/mol
Topological Polar Surface Area (TPSA) 103.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-methylsulfinyl-6'-methylthio-N,N'-di-n-hexylurea

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9382 93.82%
Caco-2 - 0.5721 57.21%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.5895 58.95%
OATP2B1 inhibitior - 0.8475 84.75%
OATP1B1 inhibitior + 0.9422 94.22%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7288 72.88%
P-glycoprotein inhibitior - 0.7962 79.62%
P-glycoprotein substrate + 0.5213 52.13%
CYP3A4 substrate - 0.5250 52.50%
CYP2C9 substrate - 0.8135 81.35%
CYP2D6 substrate - 0.7831 78.31%
CYP3A4 inhibition - 0.7587 75.87%
CYP2C9 inhibition - 0.8036 80.36%
CYP2C19 inhibition - 0.8212 82.12%
CYP2D6 inhibition - 0.9060 90.60%
CYP1A2 inhibition - 0.8522 85.22%
CYP2C8 inhibition - 0.9147 91.47%
CYP inhibitory promiscuity - 0.9726 97.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6529 65.29%
Eye corrosion - 0.9549 95.49%
Eye irritation + 0.5510 55.10%
Skin irritation - 0.7733 77.33%
Skin corrosion - 0.9176 91.76%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5856 58.56%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.5842 58.42%
skin sensitisation - 0.8378 83.78%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6082 60.82%
Acute Oral Toxicity (c) III 0.5499 54.99%
Estrogen receptor binding - 0.7081 70.81%
Androgen receptor binding - 0.6847 68.47%
Thyroid receptor binding + 0.6215 62.15%
Glucocorticoid receptor binding - 0.8542 85.42%
Aromatase binding - 0.6973 69.73%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9363 93.63%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6324 63.24%
Fish aquatic toxicity - 0.5584 55.84%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.42% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.29% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.22% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.82% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.39% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.74% 96.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.90% 94.33%
CHEMBL1968 P07099 Epoxide hydrolase 1 83.37% 98.57%
CHEMBL2179 P04062 Beta-glucocerebrosidase 82.13% 85.31%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.31% 100.00%

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 13961630
LOTUS LTS0206915
wikiData Q104394338