18 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
26638045	58	Synthesis, experimental evaluation and molecular modelling of hydroxamate derivatives as zinc metalloproteinase inhibitors.	Uit The Arctic University of Norway
25559080	38	Additivity or cooperativity: which model can predict the influence of simultaneous incorporation of two or more functionalities in a ligand molecule?	The State University of New York
23988485	5	Synthesis and enzymatic evaluation of phosphoramidon and itsß anomer: Anomerization ofa-l-rhamnose triacetate upon phosphitylation.	Jiangxi Science and Technology Normal University
22894131	4	Water mediated ligand functional group cooperativity: the contribution of a methyl group to binding affinity is enhanced by a COO(-) group through changes in the structure and thermodynamics of the hydration waters of ligand-thermolysin complexes.	The State University of New York
7783143	66	Hydroxamic acids as potent inhibitors of endothelin-converting enzyme from human bronchiolar smooth muscle.	Berlex Laboratories
8021926	41	New thiol inhibitors of neutral endopeptidase EC 3.4.24.11: synthesis and enzyme active-site recognition.	University of Paris
8340909	14	Excursions in drug discovery.	Merck Research Laboratories
1588550	10	Definition and display of steric, hydrophobic, and hydrogen-bonding properties of ligand binding sites in proteins using Lee and Richards accessible surface: validation of a high-resolution graphical tool for drug design.	Ciba-Geigy
12443790	3	Silanediol-based inhibitor of thermolysin.	State University of New York
	11	Thiol and hydroxamic acid containing inhibitors of endothelin converting enzyme	TBA
20494587	24	Identification of novel quinazolin-4(3H)-ones as inhibitors of thermolysin, the prototype of the M4 family of proteinases.	University of Troms£
	2	Inhibitory stereochemistry of N-chloroacetyl-N-hydroxyleucine methyl ester for thermolysin	TBA
19072688	22	Discovery of potent thermolysin inhibitors using structure based virtual screening and binding assays.	University of Tromsø
12951085	10	Reversed hydroxamate-bearing thermolysin inhibitors mimic a high-energy intermediate along the enzyme-catalyzed proteolytic reaction pathway.	Pohang University of Science and Technology
9934463	6	Inhibition stereochemistry of hydroxamate inhibitors for thermolysin.	Pohang University of Science and Technology
9871678	8	Inhibition of thermolysin with nitrone-bearing substrate analogs: a new type of thermolysin inhibitors.	Pohang University of Science and Technology
9046341	44	Meta-substituted benzofused macrocyclic lactams as zinc metalloprotease inhibitors.	Ciba-Geigy
9046340	23	Ortho-substituted benzofused macrocyclic lactams as zinc metalloprotease inhibitors.	Novartis Pharmaceuticals