1,5-Anhydro-2,3-dideoxy-3-(((1R,3S)-3-((7,8-dihydro-3-(trifluoromethyl)-1,6-naphthyridin-6(5H)-yl)carbonyl)-3-(1-methylethyl)cyclopentyl)amino)-4-O-methyl-D-erythro-pentitol, identified by CAS number 624733-88-6, is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups and stereocenters. This substance features a pentitol backbone, indicating it is a sugar derivative, specifically a deoxysugar, which is significant in various biochemical pathways. The presence of a trifluoromethyl group suggests potential applications in medicinal chemistry, as such groups can enhance the pharmacological properties of compounds. Additionally, the naphthyridine moiety may contribute to its biological activity, possibly influencing interactions with biological targets. The compound's stereochemistry, denoted by the (1R,3S) configuration, is crucial for its biological function, as stereoisomers can exhibit vastly different properties. Overall, this compound's unique structure positions it as a candidate for further research in drug development and other chemical applications.

1,5-anhydro-2,3-dideoxy-3-(((1r,3s)-3-((7,8-dihydro-3-(trifluoromethyl)-1,6-naphthyridin-6(5h)-yl)carbonyl)-3-(1-methylethyl)cyclopentyl)amino)-4-o-methyl-d-erythro-pentitol

624733-88-6: 1,5-Anhydro-2,3-dideoxy-3-(((1R,3S)-3-((7,8-dihydro-3-(trifluoromethyl)-1,6-naphthyridin-6(5H)-yl)carbonyl)-3-(1-methylethyl)cyclopentyl)amino)-4-O-methyl-D-erythro-pentitol, identified by CAS number 624733-88-6, is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups and stereocenters. This substance features a pentitol backbone, indicating it is a sugar derivative, specifically a deoxysugar, which is significant in various biochemical pathways. The presence of a trifluoromethyl group suggests potential applications in medicinal chemistry, as such groups can enhance the pharmacological properties of compounds. Additionally, the naphthyridine moiety may contribute to its biological activity, possibly influencing interactions with biological targets. The compound's stereochemistry, denoted by the (1R,3S) configuration, is crucial for its biological function, as stereoisomers can exhibit vastly different properties. Overall, this compound's unique structure positions it as a candidate for further research in drug development and other chemical applications.

MK-0812

<p>CCR2 chemokine receptor antagonist</p>

MK 0812

MK-0812 is a dual antagonist of the CCR2 and CCR5 receptors that can alleviate adipose inflammation in ob/ob mice.

CAS 624733-88-6

1,5-anhydro-2,3-dideoxy-3-(((1r,3s)-3-((7,8-dihydro-3-(trifluoromethyl)-1,6-naphthyridin-6(5h)-yl)carbonyl)-3-(1-methylethyl)cyclopentyl)amino)-4-o-methyl-d-erythro-pentitol

MK-0812

Ref: IN-DA00ECEB

MK 0812

Ref: 3D-FM32516

MK-0812

Ref: TM-TQ0182