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P648966-2mgPROTAC ERα Degrader-1 comprises an ubiquitin E3 ligase binding group, a linker and a protein binding group. PROTAC ERα Degrader-1 extracts from patent WO2017201449A1, compound P1. PROTAC ERα Degrader-1 is an estrogen receptor-alpha ( ERα )
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P648966-5mgPROTAC ERα Degrader-1 comprises an ubiquitin E3 ligase binding group, a linker and a protein binding group. PROTAC ERα Degrader-1 extracts from patent WO2017201449A1, compound P1. PROTAC ERα Degrader-1 is an estrogen receptor-alpha ( ERα )
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P650778-10mgPROTAC ERα Degrader-2 comprises a IAP ligand binding group, a linker and an estrogen receptor α ( ERα ) binding group. PROTAC ERα Degrader-2 is an ERα degrader. Maximal ERα degradation at 30 μM concentration in human mammary tumor MCF7 cells.
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P650778-25mgPROTAC ERα Degrader-2 comprises a IAP ligand binding group, a linker and an estrogen receptor α ( ERα ) binding group. PROTAC ERα Degrader-2 is an ERα degrader. Maximal ERα degradation at 30 μM concentration in human mammary tumor MCF7 cells.
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P650778-50mgPROTAC ERα Degrader-2 comprises a IAP ligand binding group, a linker and an estrogen receptor α ( ERα ) binding group. PROTAC ERα Degrader-2 is an ERα degrader. Maximal ERα degradation at 30 μM concentration in human mammary tumor MCF7 cells.
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P650778-5mgPROTAC ERα Degrader-2 comprises a IAP ligand binding group, a linker and an estrogen receptor α ( ERα ) binding group. PROTAC ERα Degrader-2 is an ERα degrader. Maximal ERα degradation at 30 μM concentration in human mammary tumor MCF7 cells.
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P650469-5mgPROTAC IRAK4 degrader-1 is a Cereblon -based PROTAC interleukin-1 receptor-associated kinase 4 ( IRAK4 ) degrader extracted from patent US20190192668A1 Compound I-210, makes <:20%, >:20-50%, and >:50% IRAK4 degradation at 0.01, 0.1, and 1 μM
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P650608-1mgPROTAC IRAK4 degrader-7 (Compound I-417) is an orally active PROTAC IRAK4 degrader with antitumor activitiesForm:SolidIC50&: Target:IRAK4.
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P659476-100mgPROTAC KRAS G12C degrader-1 is a Cereblon -based KRAS G12C PROTAC degrader. PROTAC KRAS G12C degrader-1 induces CRBN/ KRAS G12C dimerization and degrades GFP- KRAS G12C in reporter cells.Appearance:SolidIn Vitro:PROTAC KRAS G12C degrader-1 (Compound
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P659476-10mgPROTAC KRAS G12C degrader-1 is a Cereblon -based KRAS G12C PROTAC degrader. PROTAC KRAS G12C degrader-1 induces CRBN/ KRAS G12C dimerization and degrades GFP- KRAS G12C in reporter cells.Appearance:SolidIn Vitro:PROTAC KRAS G12C degrader-1 (Compound
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P659476-5mgPROTAC KRAS G12C degrader-1 is a Cereblon -based KRAS G12C PROTAC degrader. PROTAC KRAS G12C degrader-1 induces CRBN/ KRAS G12C dimerization and degrades GFP- KRAS G12C in reporter cells.Appearance:SolidIn Vitro:PROTAC KRAS G12C degrader-1 (Compound
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P648454-10mgPROTAC MDM2 Degrader-1 is a MDM2 degrader based on PROTAC technology. PROTAC MDM2 Degrader-1 composes of a potent MDM2 inhibitor , linker, and the MDM2 ligand for E3 ubiquitin ligaseForm:SolidIC50&: Target:MDM2.