Venetoclax D8

Venetoclax D8 Suppliers list
Company Name: Shanghai Champ Biopharmaceuticals Co., Ltd.  Gold
Tel: 021-61537865 13585780846
Email: sales@champchem.com
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Company Name: Quality Control Solutions Ltd.  
Tel: 0755-66853366 13670046396
Email: orders@qcsrm.com
Company Name: Artis Biotech Co. Ltd.  
Tel: 18108108965 18108108965
Email: sales@artisbio.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com

Venetoclax D8 manufacturers

  • Venetoclax-D8
  • Venetoclax-D8 pictures
  • $322.00
  • 2026-07-27
  • CAS:1257051-06-1
  • Purity: 99.47%
  • Supply Ability: 10g
Venetoclax D8 Basic information
Product Name:Venetoclax D8
Synonyms:Venetoclax D8;Benzamide, 4-[4-[[2-(4-chlorophenyl)-4,4-dimethyl-1-cyclohexen-1-yl]methyl]-1-piperazinyl-2,2,3,3,5,5,6,6-d8]-N-[[3-nitro-4-[[(tetrahydro-2H-pyran-4-yl)methyl]amino]phenyl]sulfonyl]-2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)-;Venetoclax-d8 (piperazine-d8);Venetoclax-d8: 2-((1H-pyrrolo[2,3-b]pyridin-5-yl)oxy)-4-(4-((4'-chloro-5,5-dimethyl-3,4,5,6-tetrahydro-[1,1'-biphenyl]-2-yl)methyl)piperazin-1-yl-2,2,3,3,5,5,6,6-d8)-N-((3-nitro-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)phenyl)sulfonyl)benzamide;D8-Venetoclax;Venetoclax-D8 (Standard);VENETOCLAX-D8
CAS:1257051-06-1
MF:C45H42ClD8N7O7S
MW:876.49
EINECS:
Product Categories:
Mol File:1257051-06-1.mol
Venetoclax D8 Structure
Venetoclax D8 Chemical Properties
form Solid
color Light yellow to yellow
Safety Information
MSDS Information
Venetoclax D8 Usage And Synthesis
UsesVenetoclax-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[1][2][3].
References[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Souers AJ, et al. ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets. Nat Med. 2013 Feb;19(2):202-8. DOI:10.1038/nm.3048
[3] Peirs S, et al. ABT-199 mediated inhibition of BCL-2 as a novel therapeutic strategy in T-cell acute lymphoblastic leukemia. Blood. 2014 Dec 11;124(25):3738-47. DOI:10.1182/blood-2014-05-574566
[4] Bi C, et al. Inhibition of 4EBP phosphorylation mediates the cytotoxic effect of mechanistic target of rapamycin kinase inhibitors in aggressive B-cell lymphomas. Haematologica. 2017 Apr;102(4):755-764. DOI:10.3324/haematol.2016.159160
Venetoclax D8 Preparation Products And Raw materials
Tag:Venetoclax D8(1257051-06-1) Related Product Information
AZD 5991 (AZD5991) DT2216 2-Butanol, 1-[(2,3-dihydro-7-methyl-1H-inden-4-yl)oxy]-3-[(1-methylethyl)amino]-, (2R,3R)-rel- ABT-263 MRT67307 CHLORIN E6