108 related articles for article (PubMed ID: 22076705)
1. Design, synthesis and cytotoxicity of novel chalcone analogs derived from 1-cyclohexylpyrrolidin-2-one and 2,3-dihydrobenzo[f]chromen-1-one.
Brien KA; Bandi RK; Behera AK; Mishra BK; Majumdar P; Satam V; Savagian M; Tzou S; Lee M; Zeller M; Robles AJ; Mooberry S; Pati H; Lee M
Arch Pharm (Weinheim); 2012 May; 345(5):341-8. PubMed ID: 22076705
[TBL] [Abstract][Full Text] [Related]
2. Design, synthesis, and cytotoxicity of novel 3-arylidenones derived from alicyclic ketones.
Satam V; Bandi RK; Behera AK; Mishra BK; Tzou S; Brockway O; Babu B; Zeller M; Westbrook C; Mooberry SL; Lee M; Pati H
Chem Biol Drug Des; 2011 Oct; 78(4):700-8. PubMed ID: 21752198
[TBL] [Abstract][Full Text] [Related]
3. Novel p-Functionalized Chromen-4-on-3-yl Chalcones Bearing Astonishing Boronic Acid Moiety as MDM2 Inhibitor: Synthesis, Cytotoxic Evaluation and Simulation Studies.
Bhatia RK; Singh L; Garg R; Kaur M; Yadav M; Madan J; Kancherla S; Pissurlenkar RRS; Coutinho EC
Med Chem; 2020; 16(2):212-228. PubMed ID: 31146672
[TBL] [Abstract][Full Text] [Related]
4. Synthesis and biological evaluation of indolyl chalcones as antitumor agents.
Kumar D; Kumar NM; Akamatsu K; Kusaka E; Harada H; Ito T
Bioorg Med Chem Lett; 2010 Jul; 20(13):3916-9. PubMed ID: 20627724
[TBL] [Abstract][Full Text] [Related]
5. Synthesis and anti-cancer activity evaluation of new dimethoxylated chalcone and flavanone analogs.
Ketabforoosh SH; Kheirollahi A; Safavi M; Esmati N; Ardestani SK; Emami S; Firoozpour L; Shafiee A; Foroumadi A
Arch Pharm (Weinheim); 2014 Nov; 347(11):853-60. PubMed ID: 25201534
[TBL] [Abstract][Full Text] [Related]
6. Design, Synthesis and Docking Studies of Flavokawain B Type Chalcones and Their Cytotoxic Effects on MCF-7 and MDA-MB-231 Cell Lines.
Abu Bakar A; Akhtar MN; Mohd Ali N; Yeap SK; Quah CK; Loh WS; Alitheen NB; Zareen S; Ul-Haq Z; Shah SAA
Molecules; 2018 Mar; 23(3):. PubMed ID: 29518053
[TBL] [Abstract][Full Text] [Related]
7. Synthesis and SAR studies of bis-chromenone derivatives for anti-proliferative activity against human cancer cells.
Venkateswararao E; Sharma VK; Manickam M; Yun J; Jung SH
Bioorg Med Chem Lett; 2014 Nov; 24(22):5256-9. PubMed ID: 25442319
[TBL] [Abstract][Full Text] [Related]
8. Heterocyclic chalcone analogues as potential anticancer agents.
Sharma V; Kumar V; Kumar P
Anticancer Agents Med Chem; 2013 Mar; 13(3):422-32. PubMed ID: 22721390
[TBL] [Abstract][Full Text] [Related]
9. Hybrid alpha-bromoacryloylamido chalcones. Design, synthesis and biological evaluation.
Romagnoli R; Baraldi PG; Carrion MD; Cruz-Lopez O; Cara CL; Balzarini J; Hamel E; Canella A; Fabbri E; Gambari R; Basso G; Viola G
Bioorg Med Chem Lett; 2009 Apr; 19(7):2022-8. PubMed ID: 19250822
[TBL] [Abstract][Full Text] [Related]
10. Design, synthesis, and biological evaluation of Mannich bases of heterocyclic chalcone analogs as cytotoxic agents.
Reddy MV; Su CR; Chiou WF; Liu YN; Chen RY; Bastow KF; Lee KH; Wu TS
Bioorg Med Chem; 2008 Aug; 16(15):7358-70. PubMed ID: 18602831
[TBL] [Abstract][Full Text] [Related]
11. Synthesis of novel β-carboline based chalcones with high cytotoxic activity against breast cancer cells.
Chauhan SS; Singh AK; Meena S; Lohani M; Singh A; Arya RK; Cheruvu SH; Sarkar J; Gayen JR; Datta D; Chauhan PM
Bioorg Med Chem Lett; 2014 Jul; 24(13):2820-4. PubMed ID: 24844196
[TBL] [Abstract][Full Text] [Related]
12. Anthraquinone-chalcone hybrids: synthesis, preliminary antiproliferative evaluation and DNA-interaction studies.
Marković V; Debeljak N; Stanojković T; Kolundžija B; Sladić D; Vujčić M; Janović B; Tanić N; Perović M; Tešić V; Antić J; Joksović MD
Eur J Med Chem; 2015 Jan; 89():401-10. PubMed ID: 25462255
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of 4'-hydroxy-3'-piperidinomethylchalcone derivatives and their cytotoxicity against PC-3 cell lines.
Gul HI; Yerdelen KO; Gul M; Das U; Pandit B; Li PK; Secen H; Sahin F
Arch Pharm (Weinheim); 2007 Apr; 340(4):195-201. PubMed ID: 17351963
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Synthesis of a series of novel dihydroartemisinin derivatives containing a substituted chalcone with greater cytotoxic effects in leukemia cells.
Yang X; Wang W; Tan J; Song D; Li M; Liu D; Jing Y; Zhao L
Bioorg Med Chem Lett; 2009 Aug; 19(15):4385-8. PubMed ID: 19501507
[TBL] [Abstract][Full Text] [Related]
16. A novel class of achiral seco-analogs of CC-1065 and the duocarmycins: design, synthesis, DNA binding, and anticancer properties.
Kupchinsky S; Centioni S; Howard T; Trzupek J; Roller S; Carnahan V; Townes H; Purnell B; Price C; Handl H; Summerville K; Johnson K; Toth J; Hudson S; Kiakos K; Hartley JA; Lee M
Bioorg Med Chem; 2004 Dec; 12(23):6221-36. PubMed ID: 15519165
[TBL] [Abstract][Full Text] [Related]
17. Synthesis and Cytotoxic Activities of Difluoro-Dimethoxy Chalcones.
Yamali C; Gul HI; Ozgun DO; Sakagam H; Umemura N; Kazaz C; Gul M
Anticancer Agents Med Chem; 2017; 17(10):1426-1433. PubMed ID: 28356013
[TBL] [Abstract][Full Text] [Related]
18. Syntheses and potential anti-prostate cancer activities of ionone-based chalcones.
Zhou J; Geng G; Batist G; Wu JH
Bioorg Med Chem Lett; 2009 Feb; 19(4):1183-6. PubMed ID: 19138519
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and cytotoxicity studies of novel 2-Hydrazonylpyrido[2,3-b]pyrazin-3(4H)-ones.
Zhang G; Liu Y; Wang S; Zhou C; Huang Q; Gong P
Arch Pharm (Weinheim); 2012 Jan; 345(1):49-56. PubMed ID: 21953529
[TBL] [Abstract][Full Text] [Related]
20. Anticancer effects of synthetic hexahydrobenzo [g]chromen-4-one derivatives on human breast cancer cell lines.
Pordeli M; Nakhjiri M; Safavi M; Ardestani SK; Foroumadi A
Breast Cancer; 2017 Mar; 24(2):299-311. PubMed ID: 27250840
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
