CAS 169181-28-6

Benzoic acid,2,4-dimethoxy-6-methyl-,4-[[4-[[(1-carboxyethyl)amino]carbonyl]-3-hydroxy-5-methylphenoxy]carbonyl]-3-hydroxy-5-methylphenylester (9CI)

Description:

Benzoic acid, 2,4-dimethoxy-6-methyl-, 4-[[4-[[(1-carboxyethyl)amino]carbonyl]-3-hydroxy-5-methylphenoxy]carbonyl]-3-hydroxy-5-methylphenyl ester, commonly referred to by its CAS number 169181-28-6, is a complex organic compound characterized by its multi-functional structure. It features a benzoic acid core with multiple substituents, including methoxy and methyl groups, which contribute to its chemical properties and potential biological activity. The presence of ester and amide functional groups suggests that it may exhibit specific reactivity patterns, such as hydrolysis or transesterification. This compound is likely to be soluble in organic solvents and may have limited solubility in water due to its hydrophobic characteristics. Its structural complexity indicates potential applications in pharmaceuticals or agrochemicals, where it may act as an intermediate or active ingredient. Additionally, the presence of hydroxyl groups may impart some degree of polarity, influencing its interactions in biological systems. Overall, this compound's unique structure positions it as a subject of interest in chemical research and development.

Formula: C₂₉H₂₉NO₁₁

Synonyms:

• AmidepsineA
• Fo 2942A

Amidepsine A

CAS: 169181-28-6

Amidepsine A is a natural product for research related to life sciences. The catalog number is T22187 and the CAS number is 169181-28-6.

Color and Shape: Solid

Molecular weight: 567.541

Ref: TM-T22187

Amidepsine A

CAS: 169181-28-6

Formula: C₂₉H₂₉NO₁₁

Molecular weight: 567.6

Ref: 7W-GL4453

Amidepsine A

Controlled Product

CAS: 169181-28-6

Formula: C₂₉H₂₉NO₁₁

Color and Shape: Neat

Molecular weight: 567.54

Ref: TR-A576680

Amidepsine A

CAS: 169181-28-6

Amidepsine A is a cyclodepsipeptide, which is derived from fungal sources, particularly marine fungi. This compound functions by inhibiting microtubule polymerization, a mode of action that disrupts cell division and affects cellular structural integrity. Amidepsine A's ability to interfere with microtubule dynamics makes it a point of interest for scientific research, particularly in the context of therapeutic applications against cancer. Inhibition of microtubule polymerization can lead to the arrest of the cell cycle, inducing apoptosis in rapidly dividing cells. This mechanism positions Amidepsine A as a potential candidate for anticancer drug development. Researchers are engaged in exploring its efficacy and specificity, seeking insights into its pharmacokinetics and potential for incorporation into chemotherapeutic regimens. The unique origin from marine fungi also prompts investigation into its biosynthesis and ecological role, contributing to the broader understanding of natural product drug discovery.

Formula: C₂₉H₂₉NO₁₁

Purity: Min. 95%

Molecular weight: 567.54 g/mol

Ref: 3D-UGA18128