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B607969-5mgBCL6 PROTAC 15.
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B658872-25mgBCN-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:Viscous liquidIC50&: Target:PEGs Alkyl/etherIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3
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B658872-50mgBCN-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:Viscous liquidIC50&: Target:PEGs Alkyl/etherIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3
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B647686-10mgBETd-246 is a second-generation and PROTAC -based BET bromodomain (BRD) inhibitor connected by ligands for Cereblon and BET , exhibiting superior selectivity, potency and antitumor activityIn VitroBETd-246 treatment (0-100 nM, 1-3 h) causes a
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B647686-25mgBETd-246 is a second-generation and PROTAC -based BET bromodomain (BRD) inhibitor connected by ligands for Cereblon and BET , exhibiting superior selectivity, potency and antitumor activityIn VitroBETd-246 treatment (0-100 nM, 1-3 h) causes a
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B647686-50mgBETd-246 is a second-generation and PROTAC -based BET bromodomain (BRD) inhibitor connected by ligands for Cereblon and BET , exhibiting superior selectivity, potency and antitumor activityIn VitroBETd-246 treatment (0-100 nM, 1-3 h) causes a
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B647686-5mgBETd-246 is a second-generation and PROTAC -based BET bromodomain (BRD) inhibitor connected by ligands for Cereblon and BET , exhibiting superior selectivity, potency and antitumor activityIn VitroBETd-246 treatment (0-100 nM, 1-3 h) causes a
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B413681-10mgInformationBI-3802 BI-3802 is a highly potent oncogenic transcription factor BCL6 degrader with strong de-repression of target genes anti-proliferative effects. BI-3802 inhibits the BTB domain of BCL6 with IC50 of ≤3 nM. BI-3802 exhibits antitumor
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B413681-1mgInformationBI-3802 BI-3802 is a highly potent oncogenic transcription factor BCL6 degrader with strong de-repression of target genes anti-proliferative effects. BI-3802 inhibits the BTB domain of BCL6 with IC50 of ≤3 nM. BI-3802 exhibits antitumor
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B413681-25mgInformationBI-3802 BI-3802 is a highly potent oncogenic transcription factor BCL6 degrader with strong de-repression of target genes anti-proliferative effects. BI-3802 inhibits the BTB domain of BCL6 with IC50 of ≤3 nM. BI-3802 exhibits antitumor
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B413681-50mgInformationBI-3802 BI-3802 is a highly potent oncogenic transcription factor BCL6 degrader with strong de-repression of target genes anti-proliferative effects. BI-3802 inhibits the BTB domain of BCL6 with IC50 of ≤3 nM. BI-3802 exhibits antitumor
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B413681-5mgInformationBI-3802 BI-3802 is a highly potent oncogenic transcription factor BCL6 degrader with strong de-repression of target genes anti-proliferative effects. BI-3802 inhibits the BTB domain of BCL6 with IC50 of ≤3 nM. BI-3802 exhibits antitumor