
CAS 2098836-45-2
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Degré de pureté (%)
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100
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90
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95
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100
3 produits concernés.
(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 :(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-methylthiDegré de pureté :98%Masse moléculaire :972.7g/molBRD4 degrader AT1
CAS :BRD4 degrader AT1 is a highly selective Brd4 degrader based on PROTAC technology, with a Kd of 44 nM for Brd4BD2 in cells.Formule :C48H58ClN9O5S3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :972.68AT 1
CAS :Produit contrôlé<p>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.<br>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.</p>Formule :C48H58ClN9O5S3Degré de pureté :Min. 95%Masse moléculaire :972.68 g/mol


