O-methyl 2-methylpropanethioate

Details

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Internal ID 7b702bab-47e9-4ec3-8402-4e928753874f
Taxonomy Organic acids and derivatives > Thiocarboxylic acids and derivatives > Thioesters
IUPAC Name O-methyl 2-methylpropanethioate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H10OS/c1-4(2)5(7)6-3/h4H,1-3H3
InChI Key WRDMVWDLJLMECM-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10OS
Molecular Weight 118.20 g/mol
Exact Mass 118.04523611 g/mol
Topological Polar Surface Area (TPSA) 41.30 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.62
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of O-methyl 2-methylpropanethioate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 - 0.7293 72.93%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4529 45.29%
OATP2B1 inhibitior - 0.8671 86.71%
OATP1B1 inhibitior + 0.9657 96.57%
OATP1B3 inhibitior + 0.9591 95.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9507 95.07%
P-glycoprotein inhibitior - 0.9749 97.49%
P-glycoprotein substrate - 0.9794 97.94%
CYP3A4 substrate - 0.7438 74.38%
CYP2C9 substrate + 0.5764 57.64%
CYP2D6 substrate - 0.8718 87.18%
CYP3A4 inhibition - 0.9616 96.16%
CYP2C9 inhibition - 0.8295 82.95%
CYP2C19 inhibition - 0.8450 84.50%
CYP2D6 inhibition - 0.9523 95.23%
CYP1A2 inhibition - 0.8362 83.62%
CYP2C8 inhibition - 0.9945 99.45%
CYP inhibitory promiscuity - 0.7946 79.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5883 58.83%
Carcinogenicity (trinary) Non-required 0.5256 52.56%
Eye corrosion + 0.8355 83.55%
Eye irritation + 0.9812 98.12%
Skin irritation + 0.5504 55.04%
Skin corrosion - 0.9531 95.31%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8172 81.72%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation + 0.6940 69.40%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.8530 85.30%
Nephrotoxicity + 0.6065 60.65%
Acute Oral Toxicity (c) III 0.7185 71.85%
Estrogen receptor binding - 0.7951 79.51%
Androgen receptor binding - 0.9111 91.11%
Thyroid receptor binding - 0.7887 78.87%
Glucocorticoid receptor binding - 0.8127 81.27%
Aromatase binding - 0.7406 74.06%
PPAR gamma - 0.8908 89.08%
Honey bee toxicity - 0.8475 84.75%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.4817 48.17%

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 87.59% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.26% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.61% 85.14%

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.
Ananas comosus

Cross-Links

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PubChem 13716562
LOTUS LTS0106590
wikiData Q104375473