CAS 57701-86-7

(1S,2S,3aR,4R,5R,7R,9S,10S,11R,13R,13aR)-1,3a,9,11,13-pentakis(acetyloxy)-4-hydroxy-2,5,8,8-tetramethyl-12-methylidene-6-oxotetradecahydro-1H-4,7-epoxycyclopenta[12]annulen-10-yl benzoate

Description:

The chemical substance with the name "(1S,2S,3aR,4R,5R,7R,9S,10S,11R,13R,13aR)-1,3a,9,11,13-pentakis(acetyloxy)-4-hydroxy-2,5,8,8-tetramethyl-12-methylidene-6-oxotetradecahydro-1H-4,7-epoxycyclopenta[12]annulen-10-yl benzoate" and CAS number "57701-86-7" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a tetradecahydro structure, indicating a saturated hydrocarbon framework with several rings. The presence of multiple acetyloxy groups suggests it has significant reactivity and potential for esterification reactions. The hydroxy group contributes to its polarity, enhancing solubility in polar solvents. Additionally, the compound's methylidene and oxo groups indicate potential sites for further chemical transformations. Its specific stereochemistry, denoted by the various R and S configurations, implies that it may exhibit unique biological activity or interactions, making it of interest in fields such as medicinal chemistry or natural product synthesis. Overall, this compound exemplifies the complexity and diversity found in organic chemistry, particularly in the realm of natural product derivatives.

Formula: C₃₇H₄₆O₁₅

InChI: InChI=1/C37H46O15/c1-17-16-36(51-24(8)42)26(28(17)46-20(4)38)29(47-21(5)39)18(2)30(48-22(6)40)31(50-34(44)25-14-12-11-13-15-25)33(49-23(7)41)35(9,10)32-27(43)19(3)37(36,45)52-32/h11-15,17,19,26,28-33,45H,2,16H2,1,3-10H3/t17-,19+,26+,28-,29-,30+,31+,32-,33+,36+,37+/m0/s1

Synonyms:

• 4,7-epoxy-6H-cyclopentacyclododecen-6-one, 1,3a,9,11,13-pentakis(acetyloxy)-10-(benzoyloxy)tetradecahydro-4-hydroxy-2,5,8,8-tetramethyl-12-methylene-, (1S,2S,3aR,4R,5R,7R,9S,10S,11R,13aR)-
• 4,7-epoxy-6H-cyclopentacyclododecen-6-one, 1,3a,9,11,13-pentakis(acetyloxy)-10-(benzoyloxy)tetradecahydro-4-hydroxy-2,5,8,8-tetramethyl-12-methylene-, (1S,2S,3aR,4R,5R,7R,9S,10S,11R,13R,13aR)-
• (1R,2R,4S,5S,6R,7R,9R,10S,11S,13R,15R)-2,5,7,9,11-Pentaacetoxy-1-hydroxy-4,12,12,15-tetramethyl-8-methylene-14-oxo-16-oxatricyclo[11.2.1.0~2,6~]hexadec-10-yl benzoate
• Kansuinine A
• 4,7-Epoxy-6H-cyclopentacyclododecen-6-one, 1,3a,9,11,13-pentakis(acetyloxy)-10-(benzoyloxy)tetradecahydro-4-hydroxy-2,5,8,8-tetramethyl-12-methylene-, (1S,2S,3aR,4R,5R,7R,9S,10S,11S,13R,13aR)-
• kansuinin A

Kansuinin A

CAS: 57701-86-7

Formula: C₃₇H₄₆O₁₅

Purity: 99.01%

Molecular weight: 730.7521

Ref: IN-DA00ELQT

Kansuinine A

CAS: 57701-86-7

Kansuinine A

Purity: ≥98%

Molecular weight: 730.75g/mol

Ref: 54-BUP00808

Kansuinin A

CAS: 57701-86-7

Formula: C₃₇H₄₆O₁₅

Purity: 95%~99%

Molecular weight: 730.76

Ref: BP-BP5230

Kansuinine A

CAS: 57701-86-7

Kansuinine A, a 95% ethanol extract from the roots of E. kansui, possesses an inhibitory effect on IL-6-induced Stat3 activation by activating ERK1/2.

Formula: C₃₇H₄₆O₁₅

Purity: 99.28%

Color and Shape: Solid

Molecular weight: 730.75

Ref: TM-TN4379

Kansuinine A

CAS: 57701-86-7

Kansuinine A is a natural alkaloid compound, which is derived from certain plant sources within the Euphorbiaceae family. This compound is notable for its specific molecular interactions that exhibit significant biological activities, particularly in the realm of anti-inflammatory and cytotoxic effects. The mode of action of Kansuinine A involves the modulation of cellular pathways that regulate inflammation, which can lead to the inhibition of pro-inflammatory cytokines and mediators.

Formula: C₃₇H₄₆O₁₅

Purity: Min. 95%

Molecular weight: 730.8 g/mol

Ref: 3D-HCA70186