Procarbazine hydrochloride

General description This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the

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CAS No.: 53-60-1

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

PROTAC CBP/P300 Degrader-1 is a potent PROTAC CBP/P300 degrader. PROTAC CBP/P300 Degrader-1 potently inhibited cell viability of multiple cancer cell linesIn VitroPROTAC CBP/P300 Degrader-1 shows LNCaP prostate cancer cell viability inhibition (IC

PRT062607 (P505-15) HCl is a novel, highly selective Syk inhibitor with IC50 of 1 nM, &gt:80-fold selective for Syk than Fgr, Lyn, FAK, Pyk2 and Zap70.

PRT062607 (P505-15) HCl is a novel, highly selective Syk inhibitor with IC50 of 1 nM, &gt:80-fold selective for Syk than Fgr, Lyn, FAK, Pyk2 and Zap70.

Biochem/physiol Actions PRT4165 is a potent inhibitor of PRC1 (polycomb-repressive complex 1)-mediated histone H2A ubiquitylation in vivo and in vitro . PRT4165 inhibits the in vitro histone H2A E3 ubiquitin ligase activity of PRC1

Biochem/physiol Actions PRT4165 is a potent inhibitor of PRC1 (polycomb-repressive complex 1)-mediated histone H2A ubiquitylation in vivo and in vitro . PRT4165 inhibits the in vitro histone H2A E3 ubiquitin ligase activity of PRC1

Pyrazin-2-ylmethanamine hydrochloride.

Pyrazin-2-ylmethanamine hydrochloride.

Pyrazin-2-ylmethanamine hydrochloride.