15 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
28621538	63	Discovery of Highly Potent and Selective Small-Molecule Reversible Factor D Inhibitors Demonstrating Alternative Complement Pathway Inhibition in Vivo.	Novartis Pharma
28157311	11	Structure-Based Library Design and Fragment Screening for the Identification of Reversible Complement Factor D Protease Inhibitors.	Novartis Institutes For Biomedical Research
27914800	11	Discovery of a new isomannide-based peptidomimetic synthetized by Ugi multicomponent reaction as human tissue kallikrein 1 inhibitor.	Universidade Federal Fluminense
27155563	5	Isocoumarins, miraculous natural products blessed with diverse pharmacological activities.	Quaid-I-Azam University
26848109	8	The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins.	Campus
26393374	34	Improving the Selectivity of Engineered Protease Inhibitors: Optimizing the P2 Prime Residue Using a Versatile Cyclic Peptide Library.	Queensland University Of Technology
25682203	13	Pyrido-imidazodiazepinones as a new class of reversible inhibitors of human kallikrein 7.	University Of Montpellier
24900785	64	Isomannide-based peptidomimetics as inhibitors for human tissue kallikreins 5 and 7.	Universidade Federal Do Abc
24211642	49	Identification by in silico and in vitro screenings of small organic molecules acting as reversible inhibitors of kallikreins.	Universit£
23849879	23	1,2,4-Triazole derivatives as transient inactivators of kallikreins involved in skin diseases.	Universit£
22959247	20	Isomannide derivatives as new class of inhibitors for human kallikrein 7.	Universidade Federal Do Tri£Ngulo Mineiro
21903387	12	Biological evaluation and docking studies of natural isocoumarins as inhibitors for human kallikrein 5 and 7.	Universidade Federal Do Tri£Ngulo Mineiro
24158442	40	Transition state analogues of Plasmodium falciparum and human orotate phosphoribosyltransferases.	Albert Einstein College Of Medicine
17028581	3	Inhibitors of Polo-like kinase reveal roles in spindle-pole maintenance.	University Of Cambridge
10715152	151	5,6-Dihydropyran-2-ones possessing various sulfonyl functionalities: potent nonpeptidic inhibitors of HIV protease.	Parke-Davis Pharmaceutical Research