These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
188 related articles for article (PubMed ID: 18827378)
1. Design and synthesis of cinanserin analogs as severe acute respiratory syndrome coronavirus 3CL protease inhibitors. Yang Q; Chen L; He X; Gao Z; Shen X; Bai D Chem Pharm Bull (Tokyo); 2008 Oct; 56(10):1400-5. PubMed ID: 18827378 [TBL] [Abstract][Full Text] [Related]
2. Cinanserin is an inhibitor of the 3C-like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro. Chen L; Gui C; Luo X; Yang Q; Günther S; Scandella E; Drosten C; Bai D; He X; Ludewig B; Chen J; Luo H; Yang Y; Yang Y; Zou J; Thiel V; Chen K; Shen J; Shen X; Jiang H J Virol; 2005 Jun; 79(11):7095-103. PubMed ID: 15890949 [TBL] [Abstract][Full Text] [Related]
3. Synthesis and evaluation of isatin derivatives as effective SARS coronavirus 3CL protease inhibitors. Chen LR; Wang YC; Lin YW; Chou SY; Chen SF; Liu LT; Wu YT; Kuo CJ; Chen TS; Juang SH Bioorg Med Chem Lett; 2005 Jun; 15(12):3058-62. PubMed ID: 15896959 [TBL] [Abstract][Full Text] [Related]
4. Discovering severe acute respiratory syndrome coronavirus 3CL protease inhibitors: virtual screening, surface plasmon resonance, and fluorescence resonance energy transfer assays. Chen L; Chen S; Gui C; Shen J; Shen X; Jiang H J Biomol Screen; 2006 Dec; 11(8):915-21. PubMed ID: 17092912 [TBL] [Abstract][Full Text] [Related]
5. Discovery of potent anilide inhibitors against the severe acute respiratory syndrome 3CL protease. Shie JJ; Fang JM; Kuo CJ; Kuo TH; Liang PH; Huang HJ; Yang WB; Lin CH; Chen JL; Wu YT; Wong CH J Med Chem; 2005 Jun; 48(13):4469-73. PubMed ID: 15974598 [TBL] [Abstract][Full Text] [Related]
6. New developments for the design, synthesis and biological evaluation of potent SARS-CoV 3CL(pro) inhibitors. Regnier T; Sarma D; Hidaka K; Bacha U; Freire E; Hayashi Y; Kiso Y Bioorg Med Chem Lett; 2009 May; 19(10):2722-7. PubMed ID: 19362479 [TBL] [Abstract][Full Text] [Related]
7. Structure-based design and synthesis of highly potent SARS-CoV 3CL protease inhibitors. Shao YM; Yang WB; Peng HP; Hsu MF; Tsai KC; Kuo TH; Wang AH; Liang PH; Lin CH; Yang AS; Wong CH Chembiochem; 2007 Sep; 8(14):1654-7. PubMed ID: 17722121 [No Abstract] [Full Text] [Related]
8. Synthesis, docking studies, and evaluation of pyrimidines as inhibitors of SARS-CoV 3CL protease. Ramajayam R; Tan KP; Liu HG; Liang PH Bioorg Med Chem Lett; 2010 Jun; 20(12):3569-72. PubMed ID: 20494577 [TBL] [Abstract][Full Text] [Related]
9. Design and synthesis of a series of serine derivatives as small molecule inhibitors of the SARS coronavirus 3CL protease. Konno H; Wakabayashi M; Takanuma D; Saito Y; Akaji K Bioorg Med Chem; 2016 Mar; 24(6):1241-54. PubMed ID: 26879854 [TBL] [Abstract][Full Text] [Related]
10. Design, synthesis, and evaluation of trifluoromethyl ketones as inhibitors of SARS-CoV 3CL protease. Shao YM; Yang WB; Kuo TH; Tsai KC; Lin CH; Yang AS; Liang PH; Wong CH Bioorg Med Chem; 2008 Apr; 16(8):4652-60. PubMed ID: 18329272 [TBL] [Abstract][Full Text] [Related]
11. Inhibitor design for SARS coronavirus main protease based on "distorted key theory". Du QS; Sun H; Chou KC Med Chem; 2007 Jan; 3(1):1-6. PubMed ID: 17266617 [TBL] [Abstract][Full Text] [Related]
12. Structure-based design, synthesis, and biological evaluation of a series of novel and reversible inhibitors for the severe acute respiratory syndrome-coronavirus papain-like protease. Ghosh AK; Takayama J; Aubin Y; Ratia K; Chaudhuri R; Baez Y; Sleeman K; Coughlin M; Nichols DB; Mulhearn DC; Prabhakar BS; Baker SC; Johnson ME; Mesecar AD J Med Chem; 2009 Aug; 52(16):5228-40. PubMed ID: 19645480 [TBL] [Abstract][Full Text] [Related]
13. Discovery of a novel family of SARS-CoV protease inhibitors by virtual screening and 3D-QSAR studies. Tsai KC; Chen SY; Liang PH; Lu IL; Mahindroo N; Hsieh HP; Chao YS; Liu L; Liu D; Lien W; Lin TH; Wu SY J Med Chem; 2006 Jun; 49(12):3485-95. PubMed ID: 16759091 [TBL] [Abstract][Full Text] [Related]
14. Synthesis and evaluation of pyrazolone compounds as SARS-coronavirus 3C-like protease inhibitors. Ramajayam R; Tan KP; Liu HG; Liang PH Bioorg Med Chem; 2010 Nov; 18(22):7849-54. PubMed ID: 20947359 [TBL] [Abstract][Full Text] [Related]
15. Development of a red-shifted fluorescence-based assay for SARS-coronavirus 3CL protease: identification of a novel class of anti-SARS agents from the tropical marine sponge Axinella corrugata. Hamill P; Hudson D; Kao RY; Chow P; Raj M; Xu H; Richer MJ; Jean F Biol Chem; 2006 Aug; 387(8):1063-74. PubMed ID: 16895476 [TBL] [Abstract][Full Text] [Related]
16. Evaluation of metal-conjugated compounds as inhibitors of 3CL protease of SARS-CoV. Hsu JT; Kuo CJ; Hsieh HP; Wang YC; Huang KK; Lin CP; Huang PF; Chen X; Liang PH FEBS Lett; 2004 Sep; 574(1-3):116-20. PubMed ID: 15358550 [TBL] [Abstract][Full Text] [Related]
17. High-throughput screening identifies inhibitors of the SARS coronavirus main proteinase. Blanchard JE; Elowe NH; Huitema C; Fortin PD; Cechetto JD; Eltis LD; Brown ED Chem Biol; 2004 Oct; 11(10):1445-53. PubMed ID: 15489171 [TBL] [Abstract][Full Text] [Related]
18. Maturation mechanism of severe acute respiratory syndrome (SARS) coronavirus 3C-like proteinase. Li C; Qi Y; Teng X; Yang Z; Wei P; Zhang C; Tan L; Zhou L; Liu Y; Lai L J Biol Chem; 2010 Sep; 285(36):28134-40. PubMed ID: 20489209 [TBL] [Abstract][Full Text] [Related]
19. Structure-based drug design and structural biology study of novel nonpeptide inhibitors of severe acute respiratory syndrome coronavirus main protease. Lu IL; Mahindroo N; Liang PH; Peng YH; Kuo CJ; Tsai KC; Hsieh HP; Chao YS; Wu SY J Med Chem; 2006 Aug; 49(17):5154-61. PubMed ID: 16913704 [TBL] [Abstract][Full Text] [Related]
20. Discovery of unsymmetrical aromatic disulfides as novel inhibitors of SARS-CoV main protease: Chemical synthesis, biological evaluation, molecular docking and 3D-QSAR study. Wang L; Bao BB; Song GQ; Chen C; Zhang XM; Lu W; Wang Z; Cai Y; Li S; Fu S; Song FH; Yang H; Wang JG Eur J Med Chem; 2017 Sep; 137():450-461. PubMed ID: 28624700 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]