6 Results for "

venetoclax abt

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "venetoclax abt" in MCE Product Catalog:

259
259 Cited Publications
Cat. No.: HY-15531
CAS No.: 1257044-40-8
Purity:  99.95%
Synonyms: abt-199; GDC-0199; RG7601
Target:  

Bcl-2 Family Autophagy

Research Areas:  

Cancer

Venetoclax (ABT-199; GDC-0199) is a highly potent, selective and orally bioavailable Bcl-2 inhibitor with a Ki of less than 0.01 nM. Venetoclax induces autophagy .
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Cat. No.: HY-15531S
CAS No.: 1257051-06-1
Purity:  99.76%
Synonyms: abt-199-d8; GDC-0199-d8; RG7601-d8
Venetoclax-d8 is deuterium labeled Venetoclax. Venetoclax (ABT-199; GDC-0199) is a highly potent, selective and orally bioavailable Bcl-2 inhibitor with a Ki of less than 0.01 nM. Venetoclax induces autophagy .
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Cat. No.: HY-15531R
CAS No.: 1257044-40-8
Synonyms: abt-199 (Standard); GDC-0199 (Standard); RG7601 (Standard)
Research Areas:  

Cancer

Venetoclax (Standard) is the analytical standard of Venetoclax. This product is intended for research and analytical applications. Venetoclax (ABT-199; GDC-0199) is a highly potent, selective and orally bioavailable Bcl-2 inhibitor with a Ki of less than 0.01 nM. Venetoclax induces autophagy .
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Cat. No.: HY-133772
CAS No.: 2469279-00-1
Target:  

Drug Metabolite

Research Areas:  

Others

Venetoclax N-oxide is an impurity of Venetoclax. Venetoclax (ABT-199; GDC-0199) is a highly potent, selective and orally bioavailable Bcl-2 inhibitor with a Ki of less than 0.01 nM .
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Cat. No.: HY-15531S1
Synonyms: abt-199-d6; GDC-0199-d6; RG7601-d6
Venetoclax-d6 (ABT-199-d6) is deuterium labeled Venetoclax. Venetoclax (ABT-199; GDC-0199) is a highly potent, selective and orally bioavailable Bcl-2 inhibitor with a Ki of less than 0.01 nM. Venetoclax induces autophagy .
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Cat. No.: HY-171334
CAS No.: 2957895-04-2
(Rac)-P1D-34 is a Pin1 PROTAC degrader that recruits cereblon, with a DC50 of 177 nM. (Rac)-P1D-34 induces Pin1 degradation via proteasome- and ubiquitin-like modification-dependent pathways. (Rac)-P1D-34 upregulates ROS and DNA damage, downregulates the UPR pathway, and inhibits leukemia cell proliferation; it also sensitizes drug-resistant acute myeloid leukemia cells to Venetoclax (ABT-199) (HY-15531) by downregulating Mcl-1 levels. (Rac)-P1D-34 can be used in the research of acute myeloid leukemia .
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