O-(2-methylpropyl) 2-(2-methylpropoxycarbothioylsulfanyl)ethylsulfanylmethanethioate

Details

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Internal ID fd3c73fc-cd7a-4dbc-b94c-9268fdbfa040
Taxonomy Organosulfur compounds > Thioacetals > Monothioacetals
IUPAC Name O-(2-methylpropyl) 2-(2-methylpropoxycarbothioylsulfanyl)ethylsulfanylmethanethioate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H22O2S4/c1-9(2)7-13-11(15)17-5-6-18-12(16)14-8-10(3)4/h9-10H,5-8H2,1-4H3
InChI Key FZTYJFQXNTUMQL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22O2S4
Molecular Weight 326.60 g/mol
Exact Mass 326.05026463 g/mol
Topological Polar Surface Area (TPSA) 133.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.37
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of O-(2-methylpropyl) 2-(2-methylpropoxycarbothioylsulfanyl)ethylsulfanylmethanethioate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 - 0.5309 53.09%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5530 55.30%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9454 94.54%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7928 79.28%
P-glycoprotein inhibitior - 0.8412 84.12%
P-glycoprotein substrate - 0.9550 95.50%
CYP3A4 substrate - 0.6494 64.94%
CYP2C9 substrate - 0.7613 76.13%
CYP2D6 substrate - 0.7532 75.32%
CYP3A4 inhibition - 0.9273 92.73%
CYP2C9 inhibition - 0.8373 83.73%
CYP2C19 inhibition - 0.7987 79.87%
CYP2D6 inhibition - 0.9394 93.94%
CYP1A2 inhibition - 0.8222 82.22%
CYP2C8 inhibition - 0.9859 98.59%
CYP inhibitory promiscuity - 0.7176 71.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.5222 52.22%
Eye corrosion + 0.8561 85.61%
Eye irritation + 0.6325 63.25%
Skin irritation - 0.6034 60.34%
Skin corrosion - 0.9455 94.55%
Ames mutagenesis - 0.6848 68.48%
Human Ether-a-go-go-Related Gene inhibition - 0.8343 83.43%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5698 56.98%
skin sensitisation + 0.8429 84.29%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.6363 63.63%
Acute Oral Toxicity (c) III 0.6596 65.96%
Estrogen receptor binding - 0.5318 53.18%
Androgen receptor binding - 0.7788 77.88%
Thyroid receptor binding + 0.7194 71.94%
Glucocorticoid receptor binding - 0.7214 72.14%
Aromatase binding - 0.8150 81.50%
PPAR gamma - 0.6970 69.70%
Honey bee toxicity - 0.9040 90.40%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8139 81.39%

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 93.62% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.69% 87.45%
CHEMBL2581 P07339 Cathepsin D 86.31% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 85.65% 95.93%
CHEMBL301 P24941 Cyclin-dependent kinase 2 84.19% 91.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.12% 99.17%

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.
There are no matching plants.

Cross-Links

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PubChem 23427972
LOTUS LTS0019394
wikiData Q105005178