225 related articles for article (PubMed ID: 26032623)
41. Synthetic ω-3 epoxyfatty acids as antiproliferative and pro-apoptotic agents in human breast cancer cells.
Dyari HR; Rawling T; Bourget K; Murray M
J Med Chem; 2014 Sep; 57(17):7459-64. PubMed ID: 25144895
[TBL] [Abstract][Full Text] [Related]
42. Anti-tumour activity of a novel coumarin-chalcone hybrid is mediated through intrinsic apoptotic pathway by inducing PUMA and altering Bax/Bcl-2 ratio.
Singh N; Sarkar J; Sashidhara KV; Ali S; Sinha S
Apoptosis; 2014 Jun; 19(6):1017-28. PubMed ID: 24638227
[TBL] [Abstract][Full Text] [Related]
43. Antiproliferative and pro-apoptotic activities of 2'- and 4'-aminochalcones against tumor canine cells.
Santos MB; Pinhanelli VC; Garcia MAR; Silva G; Baek SJ; França SC; Fachin AL; Marins M; Regasini LO
Eur J Med Chem; 2017 Sep; 138():884-889. PubMed ID: 28738308
[TBL] [Abstract][Full Text] [Related]
44. Synthesis and structure-activity relationship studies of furan-ring fused chalcones as antiproliferative agents.
Saito Y; Kishimoto M; Yoshizawa Y; Kawaii S
Anticancer Res; 2015 Feb; 35(2):811-7. PubMed ID: 25667461
[TBL] [Abstract][Full Text] [Related]
45. Design, synthesis and biological evaluations of chirally pure 1,2,3,4-tertrahydroisoquinoline analogs as anti-cancer agents.
Ramanivas T; Sushma B; Nayak VL; Chandra Shekar K; Srivastava AK
Eur J Med Chem; 2015 Mar; 92():608-18. PubMed ID: 25615796
[TBL] [Abstract][Full Text] [Related]
46. Design, synthesis, and biological evaluation of chalcone acetamide derivatives against triple negative breast cancer.
Kumar P; Singh R; Sharma D; Hassan QP; Gopu B; Anal JMH
Bioorg Med Chem Lett; 2024 Jul; 107():129795. PubMed ID: 38750906
[TBL] [Abstract][Full Text] [Related]
47. Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines.
Jacques AV; Stefanes NM; Walter LO; Perondi DM; Efe FDL; de Souza LFS; Sens L; Syracuse SM; de Moraes ACR; de Oliveira AS; Martins CT; Magalhaes LG; Andricopulo AD; Silva LO; Nunes RJ; Santos-Silva MC
Bioorg Chem; 2021 Nov; 116():105315. PubMed ID: 34496319
[TBL] [Abstract][Full Text] [Related]
48. Design, synthesis and apoptosis inducing effect of novel (Z)-3-(3'-methoxy-4'-(2-amino-2-oxoethoxy)-benzylidene)indolin-2-ones as potential antitumour agents.
Senwar KR; Reddy TS; Thummuri D; Sharma P; Naidu VG; Srinivasulu G; Shankaraiah N
Eur J Med Chem; 2016 Aug; 118():34-46. PubMed ID: 27128173
[TBL] [Abstract][Full Text] [Related]
49. Synthesis and evaluation of novel isoxazolyl chalcones as potential anticancer agents.
Wan M; Xu L; Hua L; Li A; Li S; Lu W; Pang Y; Cao C; Liu X; Jiao P
Bioorg Chem; 2014 Jun; 54():38-43. PubMed ID: 24747188
[TBL] [Abstract][Full Text] [Related]
50. Anti-breast cancer activity of heteroaryl chalcone derivatives.
Solomon VR; Lee H
Biomed Pharmacother; 2012 Apr; 66(3):213-20. PubMed ID: 22440895
[TBL] [Abstract][Full Text] [Related]
51. Synthesis and antitumor activity of novel nitrogen mustard-linked chalcones.
Fang X; Yang B; Cheng Z; Yang M; Su N; Zhou L; Zhou J
Arch Pharm (Weinheim); 2013 Apr; 346(4):292-9. PubMed ID: 23519571
[TBL] [Abstract][Full Text] [Related]
52. Inhibitors and promoters of tubulin polymerization: synthesis and biological evaluation of chalcones and related dienones as potential anticancer agents.
Dyrager C; Wickström M; Fridén-Saxin M; Friberg A; Dahlén K; Wallén EA; Gullbo J; Grøtli M; Luthman K
Bioorg Med Chem; 2011 Apr; 19(8):2659-65. PubMed ID: 21459004
[TBL] [Abstract][Full Text] [Related]
53. Synthesis of a terphenyl substituted 4-aza-2,3-didehydropodophyllotoxin analogues as inhibitors of tubulin polymerization and apoptosis inducers.
Kamal A; Tamboli JR; Nayak VL; Adil SF; Vishnuvardhan MV; Ramakrishna S
Bioorg Med Chem; 2014 May; 22(9):2714-23. PubMed ID: 24721832
[TBL] [Abstract][Full Text] [Related]
54. Synthesis and biological evaluation of conjugates of deoxypodophyllotoxin and 5-FU as inducer of caspase-3 and -7.
Huang WT; Liu J; Liu JF; Hui L; Ding YL; Chen SW
Eur J Med Chem; 2012 Mar; 49():48-54. PubMed ID: 22244588
[TBL] [Abstract][Full Text] [Related]
55. Synthesis, characterization, DNA interaction, antioxidant and anticancer activity studies of ruthenium(II) polypyridyl complexes.
Jiang GB; Xie YY; Lin GJ; Huang HL; Liang ZH; Liu YJ
J Photochem Photobiol B; 2013 Dec; 129():48-56. PubMed ID: 24177204
[TBL] [Abstract][Full Text] [Related]
56. A Novel Potent Anticancer Compound Optimized from a Natural Oridonin Scaffold Induces Apoptosis and Cell Cycle Arrest through the Mitochondrial Pathway.
Xu S; Yao H; Luo S; Zhang YK; Yang DH; Li D; Wang G; Hu M; Qiu Y; Wu X; Yao H; Xie W; Chen ZS; Xu J
J Med Chem; 2017 Feb; 60(4):1449-1468. PubMed ID: 28165738
[TBL] [Abstract][Full Text] [Related]
57. Benzylidenetetralones, cyclic chalcone analogues, induce cell cycle arrest and apoptosis in HCT116 colorectal cancer cells.
Drutovic D; Chripkova M; Pilatova M; Kruzliak P; Perjesi P; Sarissky M; Lupi M; Damia G; Broggini M; Mojzis J
Tumour Biol; 2014 Oct; 35(10):9967-75. PubMed ID: 25008568
[TBL] [Abstract][Full Text] [Related]
58. Design and synthesis of C3-pyrazole/chalcone-linked beta-carboline hybrids: antitopoisomerase I, DNA-interactive, and apoptosis-inducing anticancer agents.
Kamal A; Srinivasulu V; Nayak VL; Sathish M; Shankaraiah N; Bagul C; Reddy NV; Rangaraj N; Nagesh N
ChemMedChem; 2014 Sep; 9(9):2084-98. PubMed ID: 24470122
[TBL] [Abstract][Full Text] [Related]
59. Cytotoxicity of trans-chalcone and licochalcone A against breast cancer cells is due to apoptosis induction and cell cycle arrest.
Bortolotto LF; Barbosa FR; Silva G; Bitencourt TA; Beleboni RO; Baek SJ; Marins M; Fachin AL
Biomed Pharmacother; 2017 Jan; 85():425-433. PubMed ID: 27903423
[TBL] [Abstract][Full Text] [Related]
60. Synthesis and biological evaluation of halogenated phenoxychalcones and their corresponding pyrazolines as cytotoxic agents in human breast cancer.
Halim PA; Hassan RA; Mohamed KO; Hassanin SO; Khalil MG; Abdou AM; Osman EO
J Enzyme Inhib Med Chem; 2022 Dec; 37(1):189-201. PubMed ID: 34894967
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
