CAS 125276-62-2
:(5aR,5bR,7aS,8R,10aS,11aR,11bR,13aR)-8-(2-hydroxy-5-oxo-2,5-dihydrofuran-3-yl)-1,1,5a,7a,11b-pentamethyl-5b,6,7,7a,8,11b,13,13a-octahydrooxireno[4,4a]isochromeno[6,5-g][2]benzoxepine-3,10,12(1H,5aH,10aH)-trione
Description:
The chemical substance with the name "(5aR,5bR,7aS,8R,10aS,11aR,11bR,13aR)-8-(2-hydroxy-5-oxo-2,5-dihydrofuran-3-yl)-1,1,5a,7a,11b-pentamethyl-5b,6,7,7a,8,11b,13,13a-octahydrooxireno[4,4a]isochromeno[6,5-g][2]benzoxepine-3,10,12(1H,5aH,10aH)-trione" and CAS number "125276-62-2" is a complex organic compound characterized by a multi-ring structure that includes elements of both isochromene and benzoxepine. This compound features multiple chiral centers, indicating that it can exist in various stereoisomeric forms, which may influence its biological activity and chemical reactivity. The presence of functional groups such as hydroxyl and carbonyl groups suggests potential for hydrogen bonding and reactivity in various chemical environments. Additionally, the pentamethyl substitution indicates a high degree of alkylation, which can affect the compound's solubility and stability. Overall, this substance is likely to exhibit unique pharmacological properties, making it of interest in medicinal chemistry and drug development. Its intricate structure and functionalization may also provide insights into its mechanism of action and potential therapeutic applications.
Formula:C26H30O9
InChI:InChI=1/C26H30O9/c1-22(2)14-11-15(27)25(5)13(23(14,3)8-7-16(28)34-22)6-9-24(4)18(12-10-17(29)32-20(12)30)33-21(31)19-26(24,25)35-19/h7-8,10,13-14,18-20,30H,6,9,11H2,1-5H3/t13-,14+,18+,19-,20?,23-,24+,25+,26-/m1/s1
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Found 2 products.
Kihadanin A
CAS:<p>Kihadanin A is a natural product from Phellodendron amurense.</p>Formula:C26H30O9Purity:98%Color and Shape:SolidMolecular weight:486.51Kihadanin A
CAS:<p>Kihadanin A is a natural compound, which is a potent anti-inflammatory agent derived from the peels of citrus fruits. This compound is extracted utilizing advanced techniques to ensure purity and efficacy. Its mode of action involves the inhibition of key inflammatory pathways, particularly through the suppression of NF-kB signaling and the subsequent downregulation of pro-inflammatory cytokines. This molecular interference not only reduces inflammation but also impacts oxidative stress mechanisms within cellular environments.</p>Formula:C26H30O9Purity:Min. 95%Molecular weight:486.5 g/mol

