41 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
27240464	24	Identification, synthesis and evaluation of SARS-CoV and MERS-CoV 3C-like protease inhibitors.	Academia Sinica
21470860	9	Virtual screening identification of novel severe acute respiratory syndrome 3C-like protease inhibitors and in vitro confirmation.	Chonnam National University
19625187	22	Investigation of the pharmacophore space of Severe Acute Respiratory Syndrome coronavirus (SARS-CoV) NTPase/helicase by dihydroxychromone derivatives.	Konkuk University
19233643	16	Aryl diketoacids (ADK) selectively inhibit duplex DNA-unwinding activity of SARS coronavirus NTPase/helicase.	Konkuk University
24332657	35	Identification of novel drug scaffolds for inhibition of SARS-CoV 3-Chymotrypsin-like protease using virtual and high-throughput screenings.	University of Illinois At Chicago
24316352	27	Synthesis, modification and docking studies of 5-sulfonyl isatin derivatives as SARS-CoV 3C-like protease inhibitors.	Tianjin University of Science and Technology
24125888	2	Design, synthesis, and bioevaluation of viral 3C and 3C-like protease inhibitors.	Kansas State University
23647823	27	Dieckol, a SARS-CoV 3CL(pro) inhibitor, isolated from the edible brown algae Ecklonia cava.	Korea Research Institute of Bioscience and Biotechnology
23202846	4	Design, synthesis and crystallographic analysis of nitrile-based broad-spectrum peptidomimetic inhibitors for coronavirus 3C-like proteases.	The Chinese University of Hong Kong
20947359	18	Synthesis and evaluation of pyrazolone compounds as SARS-coronavirus 3C-like protease inhibitors.	Academia Sinica
20934345	20	Biflavonoids from Torreya nucifera displaying SARS-CoV 3CL(pro) inhibition.	Korea Research Institute of Bioscience and Biotechnology
20167482	10	SARS-CoV 3CLpro inhibitory effects of quinone-methide triterpenes from Tripterygium regelii.	Korea Research Institute of Bioscience and Biotechnology
19540764	1	Quantitative high-throughput screening identifies inhibitors of anthrax-induced cell death.	National Human Genome Research Institute
19362479	15	New developments for the design, synthesis and biological evaluation of potent SARS-CoV 3CL(pro) inhibitors.	Kyoto Pharmaceutical University
17709464	8	Novel small-molecule inhibitors of transmissible gastroenteritis virus.	National Health Research Institute
17855091	7	Structure-based design, synthesis, and biological evaluation of peptidomimetic SARS-CoV 3CLpro inhibitors.	Purdue University
29544147	36	Structure-guided design of potent and permeable inhibitors of MERS coronavirus 3CL protease that utilize a piperidine moiety as a novel design element.	Wichita State University
9884068	18	Functional effects of the muscarinic receptor agonist, xanomeline, at 5-HT1 and 5-HT2 receptors.	Smithkline Beecham Pharmaceuticals
19278250	64	A selective matrix metalloprotease 12 inhibitor for potential treatment of chronic obstructive pulmonary disease (COPD): discovery of (S)-2-(8-(methoxycarbonylamino)dibenzo[b,d]furan-3-sulfonamido)-3-methylbutanoic acid (MMP408).	Wyeth Research
19256503	32	Hit to lead account of the discovery of a new class of inhibitors of Pim kinases and crystallographic studies revealing an unusual kinase binding mode.	Boehringer Ingelheim Pharmaceuticals
19226143	17	Exploiting the pyrazolo[3,4-d]pyrimidin-4-one ring system as a useful template to obtain potent adenosine deaminase inhibitors.	Universita Di Pisa
19217779	15	Discovery and optimization of piperidyl benzamide derivatives as a novel class of 11beta-HSD1 inhibitors.	Amgen
19296695	38	Development of a novel virtual screening cascade protocol to identify potential trypanothione reductase inhibitors.	University of Alberta