CAS 50656-92-3

Aspidospermidine-3-carboxylic acid,2,3,6,7-tetradehydro-20-hydroxy-16- methoxy-,methyl ester,(5R,12â,19R,20R)-

Description:

Aspidospermidine-3-carboxylic acid, 2,3,6,7-tetradehydro-20-hydroxy-16-methoxy-, methyl ester, with the CAS number 50656-92-3, is a complex organic compound belonging to the class of alkaloids. This substance is characterized by its intricate molecular structure, which includes multiple functional groups such as carboxylic acid, methoxy, and hydroxyl groups. The presence of these functional groups contributes to its potential biological activity, particularly in pharmacology, where alkaloids are often studied for their therapeutic properties. The stereochemistry indicated by the (5R,12β,19R,20R) configuration suggests specific spatial arrangements of atoms that can influence the compound's reactivity and interaction with biological targets. Additionally, the tetradehydro configuration implies the presence of double bonds within the carbon skeleton, which can affect the compound's stability and reactivity. Overall, this compound's unique structural features make it a subject of interest in medicinal chemistry and natural product research.

Vandrikidine

CAS: 50656-92-3

Formula: C₂₂H₂₆N₂O₄

Purity: 98.0%

Color and Shape: Solid

Molecular weight: 382.4528

Ref: IN-DA00DH0Q

Vandrikidine

CAS: 50656-92-3

Vandrikidine is a natural product for research related to life sciences. The catalog number is TN5220 and the CAS number is 50656-92-3.

Formula: C₂₂H₂₆N₂O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 382.46

Ref: TM-TN5220

Vandrikidine

CAS: 50656-92-3

Formula: C₂₂H₂₆N₂O₄

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 382.46

Ref: BP-SBP01026

Vandrikidine

CAS: 50656-92-3

Vandrikidine is a synthetic compound, which is a chemically-engineered molecule created through advanced organic synthesis techniques. Its source originates from strategic modifications of known pharmacophores, aimed at enhancing specific biological activities. The mode of action of Vandrikidine involves selective inhibition of certain enzymatic pathways, leading to the modulation of key cellular processes that are critical in pathological states. This mechanistic approach allows Vandrikidine to target disease pathways with high specificity.

Formula: C₂₂H₂₆N₂O₄

Purity: Min. 95%

Molecular weight: 382.5 g/mol

Ref: 3D-ACA65692