CAS 83150-97-4

(12R)-21-Acetyloxy-13-deoxy-5β-hydroxyenmein

Description:

(12R)-21-Acetyloxy-13-deoxy-5β-hydroxyenmein, with the CAS number 83150-97-4, is a chemical compound that belongs to the class of alkaloids, specifically derived from the enmein family. This substance is characterized by its complex molecular structure, which includes multiple functional groups such as an acetoxy group and a hydroxyl group, contributing to its biological activity. The presence of the 5β-hydroxy configuration indicates a specific stereochemistry that can influence its interaction with biological systems. Alkaloids like this compound often exhibit a range of pharmacological properties, including potential anti-inflammatory and analgesic effects. The compound's solubility, stability, and reactivity can vary based on environmental conditions, such as pH and temperature. Additionally, its synthesis and extraction from natural sources may involve specific methodologies to ensure purity and yield. Overall, (12R)-21-Acetyloxy-13-deoxy-5β-hydroxyenmein represents a significant area of interest in medicinal chemistry and pharmacognosy.

Formula: C₂₂H₂₈O₈

Synonyms:

• (5beta,12alpha)-21-(Acetyloxy)-13-deoxy-5-hydroxyenmein
• Carpalasionin
• 7H-5a,8-Methano-11H-cyclohepta[c]furo[3,4-e][1]benzopyran-5,6-dione, 1-[(acetyloxy)methyl]decahydro-10,13-dihydroxy-1-methyl-7-methylene-, (1R,3aS,5aS,8S,10R,10aS,10bS,13R,13aR)-
• (12R)-21-Acetyloxy-13-deoxy-5β-hydroxyenmein

(12R)-21-Acetyloxy-13-deoxy-5β-hydroxyenmein

CAS: 83150-97-4

Formula: C₂₂H₂₈O₈

Purity: 90%

Color and Shape: Solid

Molecular weight: 420.4529

Ref: IN-DA00G8CX

Carpalasionin

CAS: 83150-97-4

Carpalasionin is a natural product from Rabdosia lasiocarpa.

Formula: C₂₂H₂₈O₈

Purity: 98%

Color and Shape: Solid

Molecular weight: 420.458

Ref: TM-TN3602

Carpalasionin

CAS: 83150-97-4

Formula: C₂₂H₂₈O₈

Purity: 95%~99%

Molecular weight: 420.458

Ref: BP-SBP03554

Carpalasionin

CAS: 83150-97-4

Carpalasionin is a synthetic bioactive compound developed through advanced organic synthesis techniques, designed to mimic complex natural structures. It is derived from a series of strategic chemical modifications and ring-closing reactions that replicate functionalities observed in naturally occurring biomolecules. The compound operates through selective binding to biological receptors and modulation of signaling pathways, thereby influencing cellular processes at a molecular level.

Formula: C₂₂H₂₈O₈

Purity: Min. 95%

Molecular weight: 420.5 g/mol

Ref: 3D-IDA15097