CAS 1255915-27-5

3-Hydroxy-N,N-dimethyl-4-[[2-[[(1R)-1-[4-(1-methylethyl)-2-furanyl]propyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]-2-pyridinecarboxamide

Description:

3-Hydroxy-N,N-dimethyl-4-[[2-[[(1R)-1-[4-(1-methylethyl)-2-furanyl]propyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]-2-pyridinecarboxamide, with CAS number 1255915-27-5, is a complex organic compound characterized by its multi-functional groups and structural diversity. It features a pyridine ring, which contributes to its potential biological activity, and a cyclobutenedione moiety that may play a role in reactivity and interaction with biological targets. The presence of hydroxyl and amine groups suggests potential for hydrogen bonding, influencing solubility and reactivity. The compound's dimethylamino group may enhance lipophilicity, affecting its pharmacokinetic properties. Additionally, the furan ring indicates potential for aromatic interactions, which can be significant in drug design and molecular recognition. Overall, this compound's intricate structure suggests it may exhibit unique chemical behavior and biological activity, making it of interest in medicinal chemistry and related fields. Further studies would be necessary to elucidate its specific properties and potential applications.

Formula: C₂₂H₂₆N₄O₅

Synonyms:

• 3-Hydroxy-N,N-dimethyl-4-[[2-[[(1R)-1-[4-(1-methylethyl)-2-furanyl]propyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]-2-pyridinecarboxamide

SQA1

CAS: 1255915-27-5

SQA1 is a derivative of a phthalamide (SQA) and acts as a CCR6 antagonist with a Kd of 250 nM, as well as a CXCR2 inhibitor. It occupies an intracellular pocket that overlaps with the G protein binding site, stabilizing the pocket's closed conformation.

Formula: C₂₂H₂₆N₄O₅

Color and Shape: Solid

Molecular weight: 426.47

Ref: TM-T88146