527 related articles for article (PubMed ID: 27217001)
21. 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]
22. Design, synthesis and biological evaluation of a series of pyrano chalcone derivatives containing indole moiety as novel anti-tubulin agents.
Wang G; Li C; He L; Lei K; Wang F; Pu Y; Yang Z; Cao D; Ma L; Chen J; Sang Y; Liang X; Xiang M; Peng A; Wei Y; Chen L
Bioorg Med Chem; 2014 Apr; 22(7):2060-79. PubMed ID: 24629450
[TBL] [Abstract][Full Text] [Related]
23. Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents.
Bhat BA; Dhar KL; Puri SC; Saxena AK; Shanmugavel M; Qazi GN
Bioorg Med Chem Lett; 2005 Jun; 15(12):3177-80. PubMed ID: 15893928
[TBL] [Abstract][Full Text] [Related]
24. DNA-binding affinity and anticancer activity of β-carboline-chalcone conjugates as potential DNA intercalators: Molecular modelling and synthesis.
Shankaraiah N; Siraj KP; Nekkanti S; Srinivasulu V; Sharma P; Senwar KR; Sathish M; Vishnuvardhan MV; Ramakrishna S; Jadala C; Nagesh N; Kamal A
Bioorg Chem; 2015 Apr; 59():130-9. PubMed ID: 25771335
[TBL] [Abstract][Full Text] [Related]
25. New chalcone-type compounds and 2-pyrazoline derivatives: synthesis and caspase-dependent anticancer activity.
Chouiter MI; Boulebd H; Pereira DM; Valentão P; Andrade PB; Belfaitah A; Silva AM
Future Med Chem; 2020 Mar; 12(6):493-509. PubMed ID: 32100558
[No Abstract] [Full Text] [Related]
26. Molecular Docking Study, Cytotoxicity, Cell Cycle Arrest and Apoptotic Induction of Novel Chalcones Incorporating Thiadiazolyl Isoquinoline in Cervical Cancer.
Tantawy MA; Sroor FM; Mohamed MF; El-Naggar ME; Saleh FM; Hassaneen HM; Abdelhamid IA
Anticancer Agents Med Chem; 2020; 20(1):70-83. PubMed ID: 31696811
[TBL] [Abstract][Full Text] [Related]
27. Design, synthesis, docking studies and biological evaluation of novel chalcone derivatives as potential histone deacetylase inhibitors.
Mohamed MFA; Shaykoon MSA; Abdelrahman MH; Elsadek BEM; Aboraia AS; Abuo-Rahma GEAA
Bioorg Chem; 2017 Jun; 72():32-41. PubMed ID: 28346873
[TBL] [Abstract][Full Text] [Related]
28. Design, synthesis, and evaluation of chalcone analogues incorporate α,β-Unsaturated ketone functionality as anti-lung cancer agents via evoking ROS to induce pyroptosis.
Zhu M; Wang J; Xie J; Chen L; Wei X; Jiang X; Bao M; Qiu Y; Chen Q; Li W; Jiang C; Zhou X; Jiang L; Qiu P; Wu J
Eur J Med Chem; 2018 Sep; 157():1395-1405. PubMed ID: 30196062
[TBL] [Abstract][Full Text] [Related]
29. Anticancer activity of novel 3-(furan-2-yl)pyrazolyl and 3-(thiophen-2-yl)pyrazolyl hybrid chalcones: Synthesis and in vitro studies.
Helmy MT; Sroor FM; Mahrous KF; Mahmoud K; Hassaneen HM; Saleh FM; Abdelhamid IA; Mohamed Teleb MA
Arch Pharm (Weinheim); 2022 Mar; 355(3):e2100381. PubMed ID: 34939695
[TBL] [Abstract][Full Text] [Related]
30. Synthesis and antiproliferative evaluation of 23-hydroxybetulinic acid derivatives.
Lan P; Wang J; Zhang DM; Shu C; Cao HH; Sun PH; Wu XM; Ye WC; Chen WM
Eur J Med Chem; 2011 Jun; 46(6):2490-502. PubMed ID: 21496972
[TBL] [Abstract][Full Text] [Related]
31. Novel chalcone derivatives as hypoxia-inducible factor (HIF)-1 inhibitor: synthesis, anti-invasive and anti-angiogenic properties.
Wang L; Chen G; Lu X; Wang S; Han S; Li Y; Ping G; Jiang X; Li H; Yang J; Wu C
Eur J Med Chem; 2015 Jan; 89():88-97. PubMed ID: 25462229
[TBL] [Abstract][Full Text] [Related]
32. Design, synthesis and cytotoxic activities of novel aliphatic amino-substituted flavonoids.
Liu G; Ge Z; Zhao M; Zhou Y
Molecules; 2013 Nov; 18(11):14070-84. PubMed ID: 24232740
[TBL] [Abstract][Full Text] [Related]
33. 1,3,4-oxadiazole/chalcone hybrids: Design, synthesis, and inhibition of leukemia cell growth and EGFR, Src, IL-6 and STAT3 activities.
Fathi MAA; Abd El-Hafeez AA; Abdelhamid D; Abbas SH; Montano MM; Abdel-Aziz M
Bioorg Chem; 2019 Mar; 84():150-163. PubMed ID: 30502626
[TBL] [Abstract][Full Text] [Related]
34. Iodine mediated pyrazolo-quinoline derivatives as potent anti-proliferative agents.
Kasaboina S; Ramineni V; Banu S; Bandi Y; Nagarapu L; Dumala N; Grover P
Bioorg Med Chem Lett; 2018 Feb; 28(4):664-667. PubMed ID: 29409753
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Synthesis and cytotoxicity of 2,5-dihydroxychalcones and related compounds.
Nam NH; Hong DH; You YJ; Kim Y; Bang SC; Kim HM; Ahn BZ
Arch Pharm Res; 2004 Jun; 27(6):581-8. PubMed ID: 15283456
[TBL] [Abstract][Full Text] [Related]
37. Design, Synthesis and Bioactivity Evaluation of Novel Chalcone Derivatives Possessing Tryptophan Moiety with Dual Activities of Anti-Cancer and Partially Restoring the Proliferation of Normal Kidney Cells Pre-Treated with Cisplatin.
He M; Yu M; Li C; Meng X; Su J; Zhu Y; Yao R
Anticancer Agents Med Chem; 2022; 22(10):1945-1961. PubMed ID: 34674626
[TBL] [Abstract][Full Text] [Related]
38. Design, synthesis, and ex vivo anti-drug resistant cervical cancer activity of novel molecularly targeted chalcone derivatives.
Yang Z; Wang Y; Ablise M; Maimaiti A; Mutalipu Z; Yan T; Liu ZY; Aihaiti A
Bioorg Chem; 2024 Aug; 149():107498. PubMed ID: 38805911
[TBL] [Abstract][Full Text] [Related]
39. Design and synthesis of novel 2'-hydroxy group substituted 2-pyridone derivatives as anticancer agents.
Lv Z; Zhang Y; Zhang M; Chen H; Sun Z; Geng D; Niu C; Li K
Eur J Med Chem; 2013 Sep; 67():447-53. PubMed ID: 23920246
[TBL] [Abstract][Full Text] [Related]
40. Synthesis and Biological Evaluation of Amino Chalcone Derivatives as Antiproliferative Agents.
Lu CF; Wang SH; Pang XJ; Zhu T; Li HL; Li QR; Li QY; Gu YF; Mu ZY; Jin MJ; Li YR; Hu YY; Zhang YB; Song J; Zhang SY
Molecules; 2020 Nov; 25(23):. PubMed ID: 33255804
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]