CAS 245660-13-3

Oxiranecarboxylic acid,3-[[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]carbonyl]-, 2-ethylester, (2S,3S)-

Description:

Oxiranecarboxylic acid, 3-[[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]carbonyl]-, 2-ethylester, (2S,3S)-, is a complex organic compound characterized by its unique structural features, including an epoxide group (oxirane), a carboxylic acid moiety, and an ester functional group. This compound exhibits chirality, with specific stereochemistry at multiple centers, which can influence its biological activity and reactivity. The presence of the hydroxyphenyl group suggests potential for hydrogen bonding and interactions with biological targets, making it of interest in medicinal chemistry. Its ester functionality may also indicate potential for hydrolysis under certain conditions, leading to the release of the corresponding acid. The compound's solubility, stability, and reactivity can vary based on environmental conditions such as pH and temperature. Overall, this substance may have applications in pharmaceuticals or agrochemicals, but further studies would be necessary to fully elucidate its properties and potential uses.

Formula: C₁₅H₁₇NO₇

Synonyms:

• 2-Oxiranecarboxylic acid, 3-[[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]carbonyl]-, 2-ethyl ester, (2S,3S)-
• SD-142

EpoY

CAS: 245660-13-3

EpoY (SD-142) is an irreversible inhibitor of the primary brain microtubule-associated tyrosine carboxypeptidase (TCP), a complex formed by vasohibin-1 (VASH1) and small vasohibin-binding protein (SVBP). By inhibiting TCP with an IC50 value of approximately 500 nM, EpoY effectively reduces the levels of detyrosinated α-tubulin, which is crucial for microtubule dynamics and neuronal differentiation. This inhibition results in significant differentiation defects and is linked to potential issues related to cancer and cardiomyopathy.

Formula: C₁₅H₁₇NO₇

Color and Shape: Solid

Molecular weight: 323.30

Ref: TM-T201297