CAS 142609-62-9
:rel-1-(3-Methylbutyl) (2R,3S)-2,3-dimercaptobutanedioate
Description:
Rel-1-(3-Methylbutyl) (2R,3S)-2,3-dimercaptobutanedioate, with the CAS number 142609-62-9, is a chemical compound characterized by its unique structure, which includes a butanedioate backbone with two mercapto (thiol) groups attached to the second and third carbon atoms. This compound is a chiral molecule, possessing two stereocenters that contribute to its specific (2R,3S) configuration. The presence of the 3-methylbutyl group enhances its hydrophobic characteristics, potentially influencing its solubility and reactivity in various environments. The mercapto groups are known for their reactivity, particularly in forming disulfide bonds, which can play a significant role in biochemical processes and interactions. This compound may be of interest in fields such as medicinal chemistry, where thiol-containing compounds are often explored for their biological activities, including antioxidant properties and potential therapeutic applications. Overall, the structural features and functional groups of this compound suggest a range of possible applications in both research and industry.
Formula:C9H16O4S2
InChI:InChI=1/C9H16O4S2/c1-5(2)3-4-13-9(12)7(15)6(14)8(10)11/h5-7,14-15H,3-4H2,1-2H3,(H,10,11)/t6-,7+/s2
InChI key:InChIKey=RIBYSYWXWXMDSW-JHPDDGAFNA-N
SMILES:[C@H](C(OCCC(C)C)=O)([C@@H](C(O)=O)S)S
Synonyms:- (2S,3R)-4-(3-methylbutoxy)-4-oxo-2,3-disulfanylbutanoic acid
- Butanedioic acid, 2,3-dimercapto-, 1-(3-methylbutyl) ester, (2R,3S)-rel-
- Butanedioic acid, 2,3-dimercapto-, mono(3-methylbutyl) ester, (2R,3S)-rel-
- Butanedioic acid, 2,3-dimercapto-, mono(3-methylbutyl) ester, (R*,S*)-
- Isoamyl 2,3-dimercaptosuccinate
- Monoisoamyl meso-2,3-dimercaptosuccinate
- Monoisoamylmeso-2,3-Dimercaptosuccinate
- rel-1-(3-Methylbutyl) (2R,3S)-2,3-dimercaptobutanedioate
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Found 2 products.
(2S,3R)-4-(3-Methylbutoxy)-4-oxo-2,3-bis-sulfanylbutanoic acid
CAS:<p>(2S,3R)-4-(3-Methylbutoxy)-4-oxo-2,3-bis-sulfanylbutanoic acid (SB203580) is a potent inhibitor of the enzyme phospholipase A2. It has been shown to inhibit mitochondrial membrane potential and neuronal death in vivo and reduce liver cell injury in vitro. SB203580 also inhibits ATP levels and enzyme activities in vivo. This drug is not carcinogenic but has been shown to interact with oxidative injury and have pharmacokinetic properties that make it clinically relevant for its use as an antiinflammatory agent.</p>Formula:C9H16O4S2Purity:Min. 95%Molecular weight:252.049


