CAS 4758-99-0

(15alpha)-15-hydroxy-21-(2-hydroxyethyl)-4-methylatida-16,20-dien-21-ium chloride

Description:

The chemical substance known as "(15alpha)-15-hydroxy-21-(2-hydroxyethyl)-4-methylatida-16,20-dien-21-ium chloride," with the CAS number 4758-99-0, is a quaternary ammonium compound that exhibits specific structural and functional characteristics. It features a steroid-like backbone, which is indicative of its potential biological activity. The presence of hydroxyl groups suggests that it may engage in hydrogen bonding, influencing its solubility and reactivity. The quaternary ammonium structure typically imparts cationic properties, making it soluble in water and suitable for various applications, including pharmaceuticals and biochemistry. Its unique configuration may also contribute to its interaction with biological membranes or receptors. Additionally, the chloride ion associated with the compound can affect its stability and solubility in different environments. Overall, this compound's structural features suggest potential utility in medicinal chemistry, particularly in the development of therapeutic agents or as a biochemical probe.

Formula: C₂₂H₃₄ClNO₂

InChI: InChI=1/C22H34NO2.ClH/c1-15-16-4-8-21(19(15)25)9-5-17-20(2)6-3-7-22(17,18(21)12-16)14-23(13-20)10-11-24;/h14,16-19,24-25H,1,3-13H2,2H3;1H/q+1;/p-1/t16?,17-,18-,19-,20?,21+,22+;/m1./s1

Guanfu base H

CAS: 4758-99-0

Guanfu base H, a diterpenoid from Aconitum coreanum, inhibits malaria strains TM4/8.2 and K1CB1 with IC50s of 4 μM, 3.6 μM.

Formula: C₂₂H₃₄ClNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 379.96

Ref: TM-T11509

Atisinium chloride

CAS: 4758-99-0

Atisinium chloride is an organometallic compound, which is synthesized through advanced coordination chemistry techniques. The source of this compound lies in the strategic combination of organic ligands with metal centers, facilitating unique interactions that are pivotal to its functionality. The mode of action primarily involves the ability to participate in complex catalytic cycles, engaging in electron transfer processes that are essential for mediating chemical transformations.

This compound finds applications in specialized fields such as catalysis, where it is utilized to promote and drive reactions that may be inefficient under normal conditions. Its effectiveness in altering reaction pathways and increasing selectivity makes it valuable in synthetic chemistry and industrial processes. Additionally, atisinium chloride's unique properties might be leveraged in materials science for the development of novel materials with tailored functionalities. The intricate balance of its reactive properties and stability under varying conditions makes it a subject of ongoing research for further applications.

Formula: C₂₂H₃₄ClNO₂

Purity: Min. 95%

Molecular weight: 379.96 g/mol

Ref: 3D-EAA75899