CAS 2098836-45-2

(2S,4R)-1-((R)-2-Acetamido-3-((6-(2-((S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)acetamido)hexyl)thio)-3-methylbutanoyl)-4-hydroxy-N-(4-(4-methylthi

CAS: 2098836-45-2

(2S,4R)-1-((R)-2-Acetamido-3-((6-(2-((S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)acetamido)hexyl)thio)-3-methylbutanoyl)-4-hydroxy-N-(4-(4-methylthi

Reinheit: 98%

Molekulargewicht: 972.7g/mol

Ref: 54-OR1073892

BRD4 degrader AT1

CAS: 2098836-45-2

BRD4 degrader AT1 is a highly selective Brd4 degrader based on PROTAC technology, with a Kd of 44 nM for Brd4BD2 in cells.

Formel: C₄₈H₅₈ClN₉O₅S₃

Reinheit: 98%

Farbe und Form: Solid

Molekulargewicht: 972.68

Ref: TM-T5439

AT 1

Kontrolliertes Produkt

CAS: 2098836-45-2

AT 1 is a peptide inhibitor of the angiotensin type 1 receptor. It is a high-affinity, potent and selective competitive inhibitor of the angiotensin type 1 receptor (AT1R). AT 1 blocks the binding of angiotensin II to AT1R, thereby inhibiting the activation of AT1R and preventing the formation of angiotensin II-induced responses.
AT 1 has been shown to inhibit cell proliferation in vitro, as well as tumor growth in vivo. This agent also inhibits protein interactions that are important for signal transduction downstream from the AT1R.

Formel: C₄₈H₅₈ClN₉O₅S₃

Reinheit: Min. 95%

Molekulargewicht: 972.68 g/mol

Ref: 3D-YID83645