Literature DB >> 23448298

A potent and highly efficacious Bcl-2/Bcl-xL inhibitor.

Angelo Aguilar1, Haibin Zhou1, Jianfang Chen1, Liu Liu1, Longchuan Bai1, Donna McEachern1, Chao-Yie Yang1, Jennifer Meagher2, Jeanne Stuckey2, Shaomeng Wang1.   

Abstract

Our previously reported Bcl-2/Bcl-xL inhibitor, 4, effectively inhibited tumor growth but failed to achieve complete regression in vivo. We have now performed extensive modifications on its pyrrole core structure, which has culminated in the discovery of 32 (BM-1074). Compound 32 binds to Bcl-2 and Bcl-xL proteins with K(i) values of <1 nM and inhibits cancer cell growth with IC50 values of 1-2 nM in four small-cell lung cancer cell lines sensitive to potent and specific Bcl-2/Bcl-xL inhibitors. Compound 32 is capable of achieving rapid, complete, and durable tumor regression in vivo at a well-tolerated dose schedule. Compound 32 is the most potent and efficacious Bcl-2/Bcl-xL inhibitor reported to date.

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Year:  2013        PMID: 23448298      PMCID: PMC3806060          DOI: 10.1021/jm4001105

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  21 in total

1.  Amino acid promoted CuI-catalyzed C-N bond formation between aryl halides and amines or N-containing heterocycles.

Authors:  Hui Zhang; Qian Cai; Dawei Ma
Journal:  J Org Chem       Date:  2005-06-24       Impact factor: 4.354

Review 2.  BH3-only proteins in cell death initiation, malignant disease and anticancer therapy.

Authors:  V Labi; M Erlacher; S Kiessling; A Villunger
Journal:  Cell Death Differ       Date:  2006-04-28       Impact factor: 15.828

3.  Bioisosteric replacements of the pyrazole moiety of rimonabant: synthesis, biological properties, and molecular modeling investigations of thiazoles, triazoles, and imidazoles as potent and selective CB1 cannabinoid receptor antagonists.

Authors:  Jos H M Lange; Herman H van Stuivenberg; Hein K A C Coolen; Tiny J P Adolfs; Andrew C McCreary; Hiskias G Keizer; Henri C Wals; Willem Veerman; Alice J M Borst; Wouter de Looff; Peter C Verveer; Chris G Kruse
Journal:  J Med Chem       Date:  2005-03-24       Impact factor: 7.446

Review 4.  Killing cancer cells by flipping the Bcl-2/Bax switch.

Authors:  Suzanne Cory; Jerry M Adams
Journal:  Cancer Cell       Date:  2005-07       Impact factor: 31.743

5.  Structure-based discovery of BM-957 as a potent small-molecule inhibitor of Bcl-2 and Bcl-xL capable of achieving complete tumor regression.

Authors:  Jianfang Chen; Haibin Zhou; Angelo Aguilar; Liu Liu; Longchuan Bai; Donna McEachern; Chao-Yie Yang; Jennifer L Meagher; Jeanne A Stuckey; Shaomeng Wang
Journal:  J Med Chem       Date:  2012-10-02       Impact factor: 7.446

6.  Bcl-2 gene promotes haemopoietic cell survival and cooperates with c-myc to immortalize pre-B cells.

Authors:  D L Vaux; S Cory; J M Adams
Journal:  Nature       Date:  1988-09-29       Impact factor: 49.962

7.  New pyrazolium-carboxylates as structural analogues of the pseudo-cross-conjugated betainic alkaloid nigellicine.

Authors:  Andreas Schmidt; Tobias Habeck; Markus Karl Kindermann; Martin Nieger
Journal:  J Org Chem       Date:  2003-07-25       Impact factor: 4.354

8.  Rational design, synthesis and biological evaluation of new 1,5-diarylpyrazole derivatives as CB1 receptor antagonists, structurally related to rimonabant.

Authors:  Giulia Menozzi; Paola Fossa; Elena Cichero; Andrea Spallarossa; Angelo Ranise; Luisa Mosti
Journal:  Eur J Med Chem       Date:  2008-02-08       Impact factor: 6.514

9.  An Improved Process for the Synthesis of 4H-Imidazo[1,5-a][1,4]benzodiazepines.

Authors:  Jie Yang; Yun Teng; Shamim Ara; Sundari Rallapalli; James M Cook
Journal:  Synthesis (Stuttg)       Date:  2009-03       Impact factor: 3.157

10.  Identification of novel binding interactions in the development of potent, selective 2-naphthamidine inhibitors of urokinase. Synthesis, structural analysis, and SAR of N-phenyl amide 6-substitution.

Authors:  Michael D Wendt; Todd W Rockway; Andrew Geyer; William McClellan; Moshe Weitzberg; Xumiao Zhao; Robert Mantei; Vicki L Nienaber; Kent Stewart; Vered Klinghofer; Vincent L Giranda
Journal:  J Med Chem       Date:  2004-01-15       Impact factor: 7.446

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  5 in total

1.  Cell death and the mitochondria: therapeutic targeting of the BCL-2 family-driven pathway.

Authors:  M J Roy; A Vom; P E Czabotar; G Lessene
Journal:  Br J Pharmacol       Date:  2014-04       Impact factor: 8.739

2.  BM-1197: a novel and specific Bcl-2/Bcl-xL inhibitor inducing complete and long-lasting tumor regression in vivo.

Authors:  Longchuan Bai; Jianfang Chen; Donna McEachern; Liu Liu; Haibin Zhou; Angelo Aguilar; Shaomeng Wang
Journal:  PLoS One       Date:  2014-06-05       Impact factor: 3.240

Review 3.  Targeting Cell Survival Proteins for Cancer Cell Death.

Authors:  Manoj K Pandey; Sahdeo Prasad; Amit Kumar Tyagi; Lokesh Deb; Jiamin Huang; Deepkamal N Karelia; Shantu G Amin; Bharat B Aggarwal
Journal:  Pharmaceuticals (Basel)       Date:  2016-02-25

4.  AlphaSpace: Fragment-Centric Topographical Mapping To Target Protein-Protein Interaction Interfaces.

Authors:  David Rooklin; Cheng Wang; Joseph Katigbak; Paramjit S Arora; Yingkai Zhang
Journal:  J Chem Inf Model       Date:  2015-08-07       Impact factor: 4.956

5.  Selective Affimers Recognise the BCL-2 Family Proteins BCL-xL and MCL-1 through Noncanonical Structural Motifs*.

Authors:  Jennifer A Miles; Fruzsina Hobor; Chi H Trinh; James Taylor; Christian Tiede; Philip R Rowell; Brian R Jackson; Fatima A Nadat; Pallavi Ramsahye; Hannah F Kyle; Basile I M Wicky; Jane Clarke; Darren C Tomlinson; Andrew J Wilson; Thomas A Edwards
Journal:  Chembiochem       Date:  2020-11-02       Impact factor: 3.164

  5 in total

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