CAS 2248552-84-1

3-Cyano-4,7-dihydro-N-(2-methoxyphenyl)-2-[[(1-methyl-1H-pyrazol-4-yl)carbonyl]amino]thieno[2,3-c]pyridine-6(5H)-carboxamide

Description:

3-Cyano-4,7-dihydro-N-(2-methoxyphenyl)-2-[[(1-methyl-1H-pyrazol-4-yl)carbonyl]amino]thieno[2,3-c]pyridine-6(5H)-carboxamide is a complex organic compound characterized by its multi-cyclic structure, which includes a thieno[2,3-c]pyridine core. This compound features a cyano group, a methoxyphenyl substituent, and a pyrazole moiety, indicating potential biological activity. The presence of the carboxamide functional group suggests it may engage in hydrogen bonding, influencing its solubility and reactivity. The compound's structure implies it could be of interest in medicinal chemistry, possibly as a lead compound for drug development, particularly in targeting specific biological pathways. Its molecular interactions may be influenced by the various functional groups present, which can affect its pharmacokinetics and pharmacodynamics. Additionally, the compound's stability, solubility, and potential toxicity would need to be evaluated in a laboratory setting to determine its suitability for further research or application. Overall, this compound exemplifies the complexity often found in drug-like molecules.

Formula: C₂₁H₂₀N₆O₃S

Synonyms:

• 3-Cyano-4,7-dihydro-N-(2-methoxyphenyl)-2-[[(1-methyl-1H-pyrazol-4-yl)carbonyl]amino]thieno[2,3-c]pyridine-6(5H)-carboxamide

WB436B

CAS: 2248552-84-1

WB436B, a highly selective STAT3 inhibitor, effectively targets and inhibits STAT3-Tyr705 phosphorylation along with the expression of STAT3 target genes. It exhibits cytotoxic effects on pancreatic cancer cells by inducing apoptosis. Furthermore, WB436B suppresses tumor growth and metastasis in pancreatic cancer mouse models, thereby prolonging the survival of tumor-bearing mice.

Formula: C₂₁H₂₀N₆O₃S

Color and Shape: Solid

Molecular weight: 436.49

Ref: TM-T200318