The chemical substance known as "(9H-fluoren-9-yl)methyl ((R)-1-(((R)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate," with the CAS number 1350456-69-7, is a complex organic compound characterized by its multi-functional structure. It features a fluorenyl group, which contributes to its aromatic properties, and a carbamate moiety that indicates potential biological activity. The presence of multiple chiral centers suggests that the compound may exhibit stereoisomerism, which can influence its pharmacological properties. Additionally, the incorporation of a hydroxymethylphenyl group and a ureidopentan-2-yl segment implies potential interactions with biological targets, making it of interest in medicinal chemistry. The compound's solubility, stability, and reactivity would depend on its specific functional groups and overall molecular architecture. Such characteristics are crucial for understanding its potential applications in drug development or as a biochemical probe. Further studies would be necessary to elucidate its specific properties and biological activities.

(9H-fluoren-9-yl)methyl ((R)-1-(((R)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate

1350456-69-7: The chemical substance known as "(9H-fluoren-9-yl)methyl ((R)-1-(((R)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate," with the CAS number 1350456-69-7, is a complex organic compound characterized by its multi-functional structure. It features a fluorenyl group, which contributes to its aromatic properties, and a carbamate moiety that indicates potential biological activity. The presence of multiple chiral centers suggests that the compound may exhibit stereoisomerism, which can influence its pharmacological properties. Additionally, the incorporation of a hydroxymethylphenyl group and a ureidopentan-2-yl segment implies potential interactions with biological targets, making it of interest in medicinal chemistry. The compound's solubility, stability, and reactivity would depend on its specific functional groups and overall molecular architecture. Such characteristics are crucial for understanding its potential applications in drug development or as a biochemical probe. Further studies would be necessary to elucidate its specific properties and biological activities.

Fmoc-D-Val-D-Cit-PAB

<p>Fmoc-D-Val-D-Cit-PAB is a cleavable linker for antibody-drug-conjugation (ADC).</p>

CAS 1350456-69-7

(9H-fluoren-9-yl)methyl ((R)-1-(((R)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate

Fmoc-D-Val-D-Cit-PAB

Ref: 54-OR1032024

Fmoc-D-Val-D-Cit-PAB

Ref: TM-T38748