CAS 2097024-37-6

1H-Benz[de]isoquinoline-1,3(2H)-dione, 2-butyl-6-(4-hydroxyphenyl)-

Description:

1H-Benz[de]isoquinoline-1,3(2H)-dione, 2-butyl-6-(4-hydroxyphenyl)-, identified by the CAS number 2097024-37-6, is a synthetic organic compound that belongs to the class of isoquinoline derivatives. This compound features a complex polycyclic structure, characterized by a benzene ring fused to an isoquinoline moiety, which is further substituted with a butyl group and a hydroxyphenyl group. The presence of the dione functional groups indicates that it has two carbonyl (C=O) functionalities, contributing to its reactivity and potential biological activity. The hydroxy group on the phenyl ring enhances its solubility in polar solvents and may also influence its interaction with biological targets. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its structural features suggest potential applications in drug development, particularly in areas related to cancer research or neuropharmacology, although specific biological activities would require further investigation through experimental studies.

Formula: C₂₂H₁₉NO₃

Synonyms:

• 1H-Benz[de]isoquinoline-1,3(2H)-dione, 2-butyl-6-(4-hydroxyphenyl)-

UGT1A1-IN-1

CAS: 2097024-37-6

UGT1A1-IN-1 (compound 2) acts as a non-competitive inhibitor of UGT1A1, effectively inhibiting the 1-O-glucuronidation process mediated by UGT1A1 with a Ki value of 5.02 μM. This compound binds to the same ligand-binding site on UGT1A1 as bilirubin and additionally functions as a 'turn-on' fluorescent probe substrate for UGT1A1 [1].

Formula: C₂₂H₁₉NO₃

Color and Shape: Solid

Molecular weight: 345.39

Ref: TM-T87592