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Volumn 43, Issue 7, 2008, Pages 669-677

Progress in small-molecule inhibitors of Bcl-2 family proteins

Author keywords

Apoptosis; Bcl 2; Drug design; Inhibitor

Indexed keywords

2 AMINO 6 BROMO 4 (1 CYANO 2 ETHOXY 2 OXOETHYL) 4H CHROMENE 3 CARBOXYLIC ACID ETHYL ESTER; 4 [4 (4' CHLORO 2 BIPHENYLYLMETHYL) 1 PIPERAZINYL] N [4 [3 DIMETHYLAMINO 1 (PHENYLTHIOMETHYL)PROPYLAMINO] 3 NITROBENZENESULFONYL]BENZAMIDE; 5 (4 BROMOBENZYLIDENE) ALPHA ISOPROPYL 4 OXO 2 THIOXO 3 THAZOLIDINEACETIC ACID; 5-(4-BROMOBENZYLIDENE)-ALPHA-ISOPROPYL-4-OXO-2-THIOXO-3-THAZOLIDINEACETIC ACID; ABT-737; ANTIMYCIN A1; ANTINEOPLASTIC AGENT; BENZOPYRAN DERIVATIVE; BIPHENYL DERIVATIVE; ETHYL 2-AMINO-6-BROMO-4-(1-CYANO-2-ETHOXY-2-OXOETHYL)-4H-CHROMENE-3-CARBOXYLATE; GOSSYPOL; HERBACEOUS AGENT; NITRILE; NITROPHENOL; PIPERAZINE DERIVATIVE; PROTEIN BCL 2; PROTEIN BCL X; SULFONAMIDE; THIAZOLE DERIVATIVE;

EID: 50549085284     PISSN: 05134870     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (4)

References (38)
  • 1
    • 5244224827 scopus 로고    scopus 로고
    • X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death [J]
    • Muchmore SW, Sattler M, Liang H, et al. X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death [J]. Nature, 1996, 381: 335-341.
    • (1996) Nature , vol.381 , pp. 335-341
    • Muchmore, S.W.1    Sattler, M.2    Liang, H.3
  • 3
    • 33744953979 scopus 로고    scopus 로고
    • Role for the Bcl-2 family proteins and BH3 domain in apoptosi [J]
    • Liu XJ, Zhang LQ, Liu XL, et al. Role for the Bcl-2 family proteins and BH3 domain in apoptosi [J]. Prog Biochem Biophys, 2006, 33:221-222.
    • (2006) Prog Biochem Biophys , vol.33 , pp. 221-222
    • Liu, X.J.1    Zhang, L.Q.2    Liu, X.L.3
  • 4
    • 34748924281 scopus 로고    scopus 로고
    • Bcl-2-regulated apoptosis; mechanism and therapeutic potential [J]
    • Adams JM, Cory S. Bcl-2-regulated apoptosis; mechanism and therapeutic potential [J]. Curr Opin Immunol, 2007, 19:488-496.
    • (2007) Curr Opin Immunol , vol.19 , pp. 488-496
    • Adams, J.M.1    Cory, S.2
  • 5
    • 0035150803 scopus 로고    scopus 로고
    • Identification of small-molecule inhibitors of interaction between the BH3 domain and Bcl-xL [J]
    • Degterev A, Lugovskoy A, Cardone M, et al. Identification of small-molecule inhibitors of interaction between the BH3 domain and Bcl-xL [J]. Nat Cell Biol, 2001, 3:173-182.
    • (2001) Nat Cell Biol , vol.3 , pp. 173-182
    • Degterev, A.1    Lugovskoy, A.2    Cardone, M.3
  • 6
    • 33846619683 scopus 로고    scopus 로고
    • Development of selective inhibitors for anti-apoptotic Bcl-2 proteins from BHI-1 [J]
    • Xing CG, Wang LY, Tang XH, et al. Development of selective inhibitors for anti-apoptotic Bcl-2 proteins from BHI-1 [J]. Bioorg Med Chem, 2007, 15:2167-2176.
    • (2007) Bioorg Med Chem , vol.15 , pp. 2167-2176
    • Xing, C.G.1    Wang, L.Y.2    Tang, X.H.3
  • 7
    • 37549071875 scopus 로고    scopus 로고
    • Development of dimeric modulators for anti-apoptotic Bcl-2 proteins [J]
    • Wang LY, Kong FS, Kokoski CL, et al. Development of dimeric modulators for anti-apoptotic Bcl-2 proteins [J]. Bioorg Med Chem Lett, 2008, 18:236-240.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 236-240
    • Wang, L.Y.1    Kong, F.S.2    Kokoski, C.L.3
  • 8
    • 0034691130 scopus 로고    scopus 로고
    • Structure-based discovery of an organic compound that binds Bcl-2 protein and induces apoptosis of tumor cells [J]
    • Wang JL, Liu DX, Zhang ZJ, et al. Structure-based discovery of an organic compound that binds Bcl-2 protein and induces apoptosis of tumor cells [J]. Proc Natl Acad Sci, 2000, 97:7124-7129.
    • (2000) Proc Natl Acad Sci , vol.97 , pp. 7124-7129
    • Wang, J.L.1    Liu, D.X.2    Zhang, Z.J.3
  • 9
    • 0242475256 scopus 로고    scopus 로고
    • HA14-1 selectively induces apoptosis in Bcl-2-overexpressing leukemia/lymphoma cells, and enhances cytarabine-induced cell death [J]
    • Lickliter JD, Wood NJ, Johnson L, et al. HA14-1 selectively induces apoptosis in Bcl-2-overexpressing leukemia/lymphoma cells, and enhances cytarabine-induced cell death [J]. Leukemia, 2003, 17: 2074-2080.
    • (2003) Leukemia , vol.17 , pp. 2074-2080
    • Lickliter, J.D.1    Wood, N.J.2    Johnson, L.3
  • 10
    • 33845940416 scopus 로고    scopus 로고
    • Structure-activity relationship studies of ethyl 2-umino-6-bromo-4-( 1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3- curboxylate (HA14-1), un antagonist for antiapoptotic Bcl-2 proteins to overcome drug resistance in cancer [J]
    • Doshi JM, Tian DF, Xing CG. Structure-activity relationship studies of ethyl 2-umino-6-bromo-4-( 1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3- curboxylate (HA14-1), un antagonist for antiapoptotic Bcl-2 proteins to overcome drug resistance in cancer [J]. J Med Chem, 2006, 49:7731-7739.
    • (2006) J Med Chem , vol.49 , pp. 7731-7739
    • Doshi, J.M.1    Tian, D.F.2    Xing, C.G.3
  • 11
    • 37549018038 scopus 로고    scopus 로고
    • Ethyl-2-amino-6-bromo-4-(1-cyano-2-ethoxy-2- oxoethyl)-4H-chromene-3-carboxylate (HA14-1), a prototype small-molecule antagonist against antiapoptotic Bcl-2 proteins, decomposes to generate reactive oxygen species that induce apoptosis [J]
    • Doshi JM, Tian DF, Xing CG. Ethyl-2-amino-6-bromo-4-(1-cyano-2-ethoxy-2- oxoethyl)-4H-chromene-3-carboxylate (HA14-1), a prototype small-molecule antagonist against antiapoptotic Bcl-2 proteins, decomposes to generate reactive oxygen species that induce apoptosis [J]. Mol Pharm, 2007, 4:919-928.
    • (2007) Mol Pharm , vol.4 , pp. 919-928
    • Doshi, J.M.1    Tian, D.F.2    Xing, C.G.3
  • 12
    • 37049008863 scopus 로고    scopus 로고
    • sHAI4-1, a stable and ROS-free antagonist against anti-apoptotic Bcl-2 proteins, bypasses drug resistances and synergizes cancer therapies in human leukemia cell [J]
    • Tian DF, Das SG, Doshi JM, et al. sHAI4-1, a stable and ROS-free antagonist against anti-apoptotic Bcl-2 proteins, bypasses drug resistances and synergizes cancer therapies in human leukemia cell [J]. Cancer Lett, 2008, 259:198-208.
    • (2008) Cancer Lett , vol.259 , pp. 198-208
    • Tian, D.F.1    Das, S.G.2    Doshi, J.M.3
  • 13
    • 0035818885 scopus 로고    scopus 로고
    • Discovery of small-molecule inhibitors of Bcl-2 through structure-based computer screening [J]
    • Enyedy IJ, Ling Y, Nacro K, et al. Discovery of small-molecule inhibitors of Bcl-2 through structure-based computer screening [J]. J Med Chem, 2001, 44:4313-4324.
    • (2001) J Med Chem , vol.44 , pp. 4313-4324
    • Enyedy, I.J.1    Ling, Y.2    Nacro, K.3
  • 14
    • 0029836953 scopus 로고    scopus 로고
    • Discovering high-affinity ligands for proteins: SAR by NMR [J]
    • Shuker SB, Hajduk PJ, Meadows RP, et al. Discovering high-affinity ligands for proteins: SAR by NMR [J]. Science, 1996, 274:1531-1535.
    • (1996) Science , vol.274 , pp. 1531-1535
    • Shuker, S.B.1    Hajduk, P.J.2    Meadows, R.P.3
  • 15
    • 31544467109 scopus 로고    scopus 로고
    • Discovery of a potent inhibitor of the antiapoptotic protein Bcl-xL from NMR and parallel synthesis [J]
    • Petros AM, Dinges J, Augeri DJ, et al. Discovery of a potent inhibitor of the antiapoptotic protein Bcl-xL from NMR and parallel synthesis [J]. J Med Chem, 2006, 49:656-663.
    • (2006) J Med Chem , vol.49 , pp. 656-663
    • Petros, A.M.1    Dinges, J.2    Augeri, D.J.3
  • 16
    • 33845570247 scopus 로고    scopus 로고
    • Design, synthesis, and computational studies of inhibitors of Bcl-xL [J]
    • Park CM, Oie T, Petros AM, et al. Design, synthesis, and computational studies of inhibitors of Bcl-xL [J]. J Am Chem Soc, 2006, 128:16206-16212.
    • (2006) J Am Chem Soc , vol.128 , pp. 16206-16212
    • Park, C.M.1    Oie, T.2    Petros, A.M.3
  • 17
    • 32344432986 scopus 로고    scopus 로고
    • Discovery and structure-activity relationship of antagonists of B-cell lymphoma 2 family proteins with chemopotentiation activity in vitro and in vivo [J]
    • Wendt MD, Shen W, Kunzer A, et al. Discovery and structure-activity relationship of antagonists of B-cell lymphoma 2 family proteins with chemopotentiation activity in vitro and in vivo [J]. J Med Chem, 2006, 49: 1165-1181.
    • (2006) J Med Chem , vol.49 , pp. 1165-1181
    • Wendt, M.D.1    Shen, W.2    Kunzer, A.3
  • 18
    • 33847404358 scopus 로고    scopus 로고
    • Studies leading to potent, dual inhibitors of Bcl-2 and Bcl-xL [J]
    • Bruncko M, Oost TK, Belli BA, et al. Studies leading to potent, dual inhibitors of Bcl-2 and Bcl-xL [J]. J Med Chem, 2007, 50:641-662.
    • (2007) J Med Chem , vol.50 , pp. 641-662
    • Bruncko, M.1    Oost, T.K.2    Belli, B.A.3
  • 19
    • 20444486559 scopus 로고    scopus 로고
    • An inhibitor of Bcl-2 family proteins induces regression of solid tumours [J]
    • Oltersdorf T, Elmore SW, Shoemaker AR, et al. An inhibitor of Bcl-2 family proteins induces regression of solid tumours [J]. Nature, 2005, 435:677-681.
    • (2005) Nature , vol.435 , pp. 677-681
    • Oltersdorf, T.1    Elmore, S.W.2    Shoemaker, A.R.3
  • 20
    • 33845994359 scopus 로고    scopus 로고
    • Chronic lymphocytic leukemia requires Bcl-2 to sequester prodeath BIM, explaining sensitivity to Bcl-2 antagonist ABT-737 [J]
    • Gaizo Moore VD, Brown JR, Certo M, et al. Chronic lymphocytic leukemia requires Bcl-2 to sequester prodeath BIM, explaining sensitivity to Bcl-2 antagonist ABT-737 [J]. J Clin Inves, 2007, 117:112-121.
    • (2007) J Clin Inves , vol.117 , pp. 112-121
    • Gaizo Moore, V.D.1    Brown, J.R.2    Certo, M.3
  • 21
    • 33750834023 scopus 로고    scopus 로고
    • The BH3 mimetic ABT-737 targets selective Bcl-2 proteins and efficiently induces apoptosis via Bak/Bax if Mcl-1 is neutralized [J]
    • Van Delft M, Wei A, Mason K, et al. The BH3 mimetic ABT-737 targets selective Bcl-2 proteins and efficiently induces apoptosis via Bak/Bax if Mcl-1 is neutralized [J]. Cancer Cell, 2006, 10:389-399.
    • (2006) Cancer Cell , vol.10 , pp. 389-399
    • Van Delft, M.1    Wei, A.2    Mason, K.3
  • 22
    • 46949107312 scopus 로고    scopus 로고
    • Novel small molecule promotes programmed cell death; "new drugs on the horizon" session [AACR annual meeting] [J]
    • Tuma RS. Novel small molecule promotes programmed cell death; "new drugs on the horizon" session [AACR annual meeting] [J]. Oncol Times, 2007, 29:38-40.
    • (2007) Oncol Times , vol.29 , pp. 38-40
    • Tuma, R.S.1
  • 23
    • 50549087313 scopus 로고    scopus 로고
    • Discovery of ABT-263, an orally active small molecule inhibitor of anti-apoptotic Bcl-2 family proteins [C]
    • Park CM. Discovery of ABT-263, an orally active small molecule inhibitor of anti-apoptotic Bcl-2 family proteins [C]. American Chemical Society Western Regional Meeting, 2007.
    • (2007) American Chemical Society Western Regional Meeting
    • Park, C.M.1
  • 24
    • 50549086114 scopus 로고    scopus 로고
    • Wang S, Yang D. Small molecule inhibitor targeted at Bcl-2: CN, 1589135A[P], 2005-03-02.
    • Wang S, Yang D. Small molecule inhibitor targeted at Bcl-2: CN, 1589135A[P], 2005-03-02.
  • 25
    • 0141569444 scopus 로고    scopus 로고
    • Discovery, characterization, and structure-activity relationships studies of proapoptotic polyphenols targeting B-cell lymphocyte/leukemia-2 proteins [J]
    • Kitada S, Leone M, Sareth S, et al. Discovery, characterization, and structure-activity relationships studies of proapoptotic polyphenols targeting B-cell lymphocyte/leukemia-2 proteins [J]. J Med Chem, 2006, 46:4259-4264.
    • (2006) J Med Chem , vol.46 , pp. 4259-4264
    • Kitada, S.1    Leone, M.2    Sareth, S.3
  • 26
    • 33750112776 scopus 로고    scopus 로고
    • Structure-based design of potent small-molecule inhibitors of anti-apoptotic Bcl-2 proteins [ J]
    • Wang GP, Nikolovska-Coleska Z, Yang CY, et al. Structure-based design of potent small-molecule inhibitors of anti-apoptotic Bcl-2 proteins [ J]. J Med Chem, 2006, 49:6139-6142.
    • (2006) J Med Chem , vol.49 , pp. 6139-6142
    • Wang, G.P.1    Nikolovska-Coleska, Z.2    Yang, C.Y.3
  • 27
    • 33749023071 scopus 로고    scopus 로고
    • Antiangiogenic effect of TW37, a small-molecule inhibitor of Bcl-2 [J]
    • Zeitlin BD, Joo E, Dong ZH, et al. Antiangiogenic effect of TW37, a small-molecule inhibitor of Bcl-2 [J]. Cancer Res, 2006, 66:8698-8706.
    • (2006) Cancer Res , vol.66 , pp. 8698-8706
    • Zeitlin, B.D.1    Joo, E.2    Dong, Z.H.3
  • 28
    • 34247276084 scopus 로고    scopus 로고
    • Pyrogallol-based molecules as potent inhibitors of the antiapoptotic Bcl-2 proteins [J]
    • Tang GZ, Yang CY, Nikolovska-Coleska Z, et al. Pyrogallol-based molecules as potent inhibitors of the antiapoptotic Bcl-2 proteins [J]. J Med Chem, 2007, 50:1723-1726.
    • (2007) J Med Chem , vol.50 , pp. 1723-1726
    • Tang, G.Z.1    Yang, C.Y.2    Nikolovska-Coleska, Z.3
  • 29
    • 39749116193 scopus 로고    scopus 로고
    • Acylpyrogallols as inhibitors of antiapoptotic Bcl-2 proteins [J]
    • Tang GZ, Nikolovska-Coleska Z, Qiu S, et al. Acylpyrogallols as inhibitors of antiapoptotic Bcl-2 proteins [J]. J Med Chem, 2008, 51:717-720.
    • (2008) J Med Chem , vol.51 , pp. 717-720
    • Tang, G.Z.1    Nikolovska-Coleska, Z.2    Qiu, S.3
  • 30
    • 34447548988 scopus 로고    scopus 로고
    • Structure-based design of flavonoid compounds as a new class of small-molecule inhibitors of the anti-apoptotic Bcl-2 proteins [J]
    • Tang GZ, Ding K, Nikolovska-Coleska Z, et al. Structure-based design of flavonoid compounds as a new class of small-molecule inhibitors of the anti-apoptotic Bcl-2 proteins [J]. J Med Chem, 2007, 50:3163-3166.
    • (2007) J Med Chem , vol.50 , pp. 3163-3166
    • Tang, G.Z.1    Ding, K.2    Nikolovska-Coleska, Z.3
  • 31
    • 22944431902 scopus 로고    scopus 로고
    • Terphenyl-based Bak BH3 r-helical proteomimetics as low-molecular-weight antagonists of Bcl-xL [J]
    • Yin H, Lee GI, Sedey KA, et al. Terphenyl-based Bak BH3 r-helical proteomimetics as low-molecular-weight antagonists of Bcl-xL [J]. J Am Chem Soc, 2005, 27: 10191-10196.
    • (2005) J Am Chem Soc , vol.27 , pp. 10191-10196
    • Yin, H.1    Lee, G.I.2    Sedey, K.A.3
  • 33
    • 0035147650 scopus 로고    scopus 로고
    • Antimycin a mimics a cell-death-inducing Bcl-2 homology domain 3 [J]
    • Tzung SP, Kim KM, Basanez G, et al. Antimycin a mimics a cell-death-inducing Bcl-2 homology domain 3 [J]. Nat Cell Biol, 2001, 3:183-191.
    • (2001) Nat Cell Biol , vol.3 , pp. 183-191
    • Tzung, S.P.1    Kim, K.M.2    Basanez, G.3
  • 34
    • 34548127040 scopus 로고    scopus 로고
    • Curcumin down-regulates Ets-1 and Bcl-2 expression in human endometrial carcinoma HEC-1-A cells [J]
    • Yu ZM, Shah DM. Curcumin down-regulates Ets-1 and Bcl-2 expression in human endometrial carcinoma HEC-1-A cells [J]. Gynecol Oncol, 2007, 106:541-548.
    • (2007) Gynecol Oncol , vol.106 , pp. 541-548
    • Yu, Z.M.1    Shah, D.M.2
  • 35
    • 33748360634 scopus 로고    scopus 로고
    • Oridonin induced U937 cell apoptosis through ERK pathway [J]
    • Liu YQ, You S, Shinichi T, et al. Oridonin induced U937 cell apoptosis through ERK pathway [J]. China J Chin Mater Med, 2005, 30:1856-1859.
    • (2005) China J Chin Mater Med , vol.30 , pp. 1856-1859
    • Liu, Y.Q.1    You, S.2    Shinichi, T.3
  • 36
    • 34648819090 scopus 로고    scopus 로고
    • A novel small molecule inhibitor targeted at Bcl-2 [J]. Sci China Ser C-Life
    • Jin LJ, Zhang ZC, Wang YY, et al. A novel small molecule inhibitor targeted at Bcl-2 [J]. Sci China Ser C-Life Sci, 2007, 50:624-629.
    • (2007) Sci , vol.50 , pp. 624-629
    • Jin, L.J.1    Zhang, Z.C.2    Wang, Y.Y.3
  • 37
    • 34547666802 scopus 로고    scopus 로고
    • Construction of a three-dimensional pharmacophore for Bcl-2 inhibitors by flexible docking and the multiple copy simultaneous search method [J]
    • Zheng CH, Zhou YJ, Zhu J, et al. Construction of a three-dimensional pharmacophore for Bcl-2 inhibitors by flexible docking and the multiple copy simultaneous search method [J]. Bioorg Med Chem, 2007, 15:6407-6417.
    • (2007) Bioorg Med Chem , vol.15 , pp. 6407-6417
    • Zheng, C.H.1    Zhou, Y.J.2    Zhu, J.3
  • 38
    • 4344559672 scopus 로고    scopus 로고
    • Molecular dynamics study of peptide segments of the BH3 domain of the proapoptotic proteins Bak, Bax, Bid and Hrk bound to the Bcl-xL and Bcl-2 proteins [J]
    • Pinto M, Perez JJ, Rubio-Martinez J. Molecular dynamics study of peptide segments of the BH3 domain of the proapoptotic proteins Bak, Bax, Bid and Hrk bound to the Bcl-xL and Bcl-2 proteins [J]. J Comput Aided Mol Des, 2004, 18:13-22.
    • (2004) J Comput Aided Mol Des , vol.18 , pp. 13-22
    • Pinto, M.1    Perez, J.J.2    Rubio-Martinez, J.3


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