Carbothioic Derivatives
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Filtered Search Results
eMolecules 10387-40-3 | Potassium thioacetate | Oakwood Chemicals | MFCD00137704 | 114.200 | C2H3KOS | 97.000 | [K+].CC([S-])=O | 1g | 480134878
Potassium thioacetate | Oakwood Chemicals | 10387-40-3 | MFCD00137704 | 114.200 | C2H3KOS | 97.000 | [K+].CC([S-])=O | 1g | 480134878
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Sigma Aldrich Fine Chemicals Biosciences Spironolactone | 52-01-7 | MFCD00082250 | 1 g
Spironolactone | Purity: 97.0-103.0% | Mol Wt: 416.57 | 52-01-7 | MFCD00082250 | 1 g
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Sigma Aldrich Fine Chemicals Biosciences Homocysteine Assay Kit suf
Homocysteine is a non-proteogenic amino acid synthesized intracellularly by removal of the N-methyl group from the essential amino acid methionine. Homocysteine is exported from cells into the blood where it exists mainly as an oxidized disulfide species either as a dimer or bound to cysteine residues of serum proteins. The reduced form of homocysteine (free homocysteine) can be metabolized into cysteine via the transsulfuration pathway however it can also undergo intramolecular cyclization forming the highly reactive pro-oxidant homocysteine thiolactone. Subsequent N-homocysteinylation of protein lysine residues by the reactive thiolactone disrupts protein conformation leading to formation of cytotoxic protein aggregates. Homocysteinylated proteins may also act as autoantigens triggering arterial inflammation and atherosclerosis. Elevated plasma homocysteine concentration is a clinical biomarker for increased risk of cardiovascular disease ischemic stroke and myocardial infarct
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Cayman Chemical NbutyrylLHomocysteine thiolac
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An analog of N-butyryl-L-HSL, the small diffusible signaling molecule involved in quorum sensing, controlling gene expression, and cellular metabolism; induces violacein expression in C. violaceum mutants usually not able to produce AHLs
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Ambeed AMBEED
NC3991910 L-HOMOCYSTEINE THIOLACTONE HCL
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Cayman Chemical S-Farnsyl ThIoacetIc AcId 50mg
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A competitive inhibitor of isoprenylated protein methyltransferase (also known as S-adenosylmethionine-dependent methyltransferase)
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S-Ethyl Trifluorothioacetate 99%, Thermo Scientific™
CAS: 383-64-2 Molecular Formula: C4H5F3OS Molecular Weight (g/mol): 158.138 InChI Key: VGGUKFAVHPGNBF-UHFFFAOYSA-N Synonym: s-ethyl trifluorothioacetate,ethanethioic acid, trifluoro-, s-ethyl ester,ethyl trifluorothiolacetate,s-ethyl trifluoroethanethioate,trifluoroacetonylmercaptoethanol,acetic acid, trifluorothio-, s-ethyl ester,s-ethylthiotrifluoroacetate,trifluorothioacetic acid s-ethyl ester,ethanethioic acid, 2,2,2-trifluoro-, s-ethyl ester,1-ethylsulfanyl-2,2,2-trifluoroethanone PubChem CID: 67844 IUPAC Name: S-ethyl 2,2,2-trifluoroethanethioate SMILES: CCSC(=O)C(F)(F)F
| PubChem CID | 67844 |
|---|---|
| CAS | 383-64-2 |
| Molecular Weight (g/mol) | 158.138 |
| SMILES | CCSC(=O)C(F)(F)F |
| Synonym | s-ethyl trifluorothioacetate,ethanethioic acid, trifluoro-, s-ethyl ester,ethyl trifluorothiolacetate,s-ethyl trifluoroethanethioate,trifluoroacetonylmercaptoethanol,acetic acid, trifluorothio-, s-ethyl ester,s-ethylthiotrifluoroacetate,trifluorothioacetic acid s-ethyl ester,ethanethioic acid, 2,2,2-trifluoro-, s-ethyl ester,1-ethylsulfanyl-2,2,2-trifluoroethanone |
| IUPAC Name | S-ethyl 2,2,2-trifluoroethanethioate |
| InChI Key | VGGUKFAVHPGNBF-UHFFFAOYSA-N |
| Molecular Formula | C4H5F3OS |
S-Methyl 2-Furancarbothioate 98.0+%, TCI America™
CAS: 13679-61-3 Molecular Formula: C6H6O2S Molecular Weight (g/mol): 142.172 MDL Number: MFCD00040266 InChI Key: ISKUAGFDTRLBHG-UHFFFAOYSA-N Synonym: 2-Furancarbothioic Acid S-Methyl Ester, S-Methyl 2-Thiofuroate, 2-Thiofuroic Acid S-Methyl Ester PubChem CID: 61662 IUPAC Name: S-methyl furan-2-carbothioate SMILES: CSC(=O)C1=CC=CO1
| PubChem CID | 61662 |
|---|---|
| CAS | 13679-61-3 |
| Molecular Weight (g/mol) | 142.172 |
| MDL Number | MFCD00040266 |
| SMILES | CSC(=O)C1=CC=CO1 |
| Synonym | 2-Furancarbothioic Acid S-Methyl Ester, S-Methyl 2-Thiofuroate, 2-Thiofuroic Acid S-Methyl Ester |
| IUPAC Name | S-methyl furan-2-carbothioate |
| InChI Key | ISKUAGFDTRLBHG-UHFFFAOYSA-N |
| Molecular Formula | C6H6O2S |