36 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
722731	1	Prodrugs of 9-beta-D-arabinofuranosyladenine. 1. Synthesis and evaluation of some 5'-(O-acyl) derivatives.	TBA
10450967	4	The design and synthesis of inhibitors of adenosine 5'-monophosphate deaminase.	Agrevo
21138280	33	Investigations into the origin of the molecular recognition of several adenosine deaminase inhibitors.	Bar-Ilan University
16078836	13	Novel, highly potent adenosine deaminase inhibitors containing the pyrazolo[3,4-d]pyrimidine ring system. Synthesis, structure-activity relationships, and molecular modeling studies.	Universit£
14761206	10	Inhibition of adenosine deaminase by novel 5:7 fused heterocycles containing the imidazo[4,5-e][1,2,4]triazepine ring system: a structure-activity relationship study.	University of Maryland
11606136	10	Design, synthesis, and biological evaluation of novel nucleoside and nucleotide analogues as agents against DNA viruses and/or retroviruses.	Academia Sinica
11101360	14	Adenosine deaminase inhibitors: synthesis and biological evaluation of unsaturated, aromatic, and oxo derivatives of (+)-erythro-9-(2'S-hydroxy-3'R-nonyl)adenine [(+)-EHNA].	University of Rhode Island
9397178	1	Enzymatic properties of the unnatural beta-L-enantiomers of 2',3'-dideoxyadenosine and 2',3'-didehydro-2',3'-dideoxyadenosine.	University of Montpellier
7562937	48	Synthesis and biological evaluation of N6-cycloalkyl derivatives of 1-deazaadenine nucleosides: a new class of anti-human immunodeficiency virus agents.	Universit£
8289197	20	Adenosine deaminase inhibitors: synthesis and structure-activity relationships of 2-hydroxy-3-nonyl derivatives of azoles.	Universit£
1433220	12	Adenosine deaminase inhibitors. Synthesis and biological evaluation of C1' and nor-C1' derivatives of (+)-erythro-9-(2(S)-hydroxy-3(R)-nonyl)adenine.	University of Rhode Island
2066996	4	Purine and 1-deazapurine ribonucleosides and deoxyribonucleosides: synthesis and biological activity.	Universit£
2002459	28	Adenosine deaminase inhibitors: synthesis and structure-activity relationships of imidazole analogues of erythro-9-(2-hydroxy-3-nonyl)adenine.	Universit£
3339608	10	Adenosine deaminase inhibitors. Synthesis and biological activity of deaza analogues of erythro-9-(2-hydroxy-3-nonyl)adenine.	Universit£
3585903	2	Synthesis, structure, and biological activity of certain 2-deoxy-beta-D-ribo-hexopyranosyl nucleosides and nucleotides.	TBA
4068002	2	Study on the inhibition of adenosine deaminase.	TBA
6699873	10	Adenosine deaminase inhibitors. Synthesis of deaza analogues of erythro-9-(2-hydroxy-3-nonyl)adenine.	TBA
6604819	5	Adenosine deaminase inhibitors. Synthesis and biological evaluation of (+/-)-3,6,7,8-tetrahydro-3-[(2-hydroxyethoxy)methyl]imidazo[4,5-d] [1,3]diazepin-8-ol and some selected C-5 homologues of pentostatin.	TBA
11677121	4	A unique ring-expanded acyclic nucleoside analogue that inhibits both adenosine deaminase (ADA) and guanine deaminase (GDA; guanase): synthesis and enzyme inhibition studies of 4,6-diamino-8H-1-hydroxyethoxymethyl-8-iminoimidazo[4,5-e][1,3]diazepine.	University of Maryland
	4	Adenosine deaminase inhibitors. Synthesis and biological evaluation of chain modified analogs of (+)-EHNA	TBA
11356110	2	Synthesis and biological evaluation of purine-containing butenolides.	Academia Sinica
11170651	47	AMP deaminase inhibitors. 5. Design, synthesis, and SAR of a highly potent inhibitor series.	Metabasis Therapeutics
10780908	40	AMP deaminase inhibitors. 4. Further N3-substituted coformycin aglycon analogues: N3-alkylmalonates as ribose 5'-monophosphate mimetics.	Metabasis Therapeutics
10780907	63	AMP deaminase inhibitors. 3. SAR of 3-(carboxyarylalkyl)coformycin aglycon analogues.	Metabasis Therapeutics
10780906	94	AMP deaminase inhibitors. 2. Initial discovery of a non-nucleotide transition-state inhibitor series.	Metabasis Therapeutics
9873405	9	Adenosine deaminase inhibitors. Synthesis and biological evaluation of aralkyladenines (ARADS).	University of Rhode Island
9341908	2	Effect of a chemical modification on the hydrated adenosine intermediate produced by adenosine deaminase and a model reaction for a potential mechanism of action of 5-aminoimidazole ribonucleotide carboxylase.	Southern Illinois University
8295218	3	Adenosine deaminase inhibitors. Synthesis and biological evaluation of 4-amino-1-(2(S)-hydroxy-3(R)-nonyl)-1H-imidazo[4,5-c]pyridine (3-deaza-(+)-EHNA) and certain C1' derivatives.	University of Rhode Island
7966142	4	Adenosine deaminase inhibitors. Synthesis and biological evaluation of putative metabolites of (+)-erythro-9-(2S-hydroxy-3R-nonyl)adenine.	University of Rhode Island
7473592	2	Design, synthesis, and structure-activity relationship of novel dinucleotide analogs as agents against herpes and human immunodeficiency viruses.	Academia Sinica
7401106	21	Heat-induced formation of alpha,beta-unsaturated nucleoside dialdehydes and their activity with adenosine deaminase.	TBA
7086847	4	Inhibitors of adenosine deaminase. Studies in combining high-affinity enzyme-binding structural units. erythro-1,6-Dihydro-6-(hydroxymethyl)-9-(2-hydroxy-3-nonyl)purine and erythro-9-(2-hydroxy-3-nonyl)purine.	TBA
6965728	5	Binding specificities of adenosine aminohydrolase from calf intestinal mucosa with dialdehydes derived from hexofuranosyladenine nucleosides.	TBA
28951094	27	Modifications of flexible nonyl chain and nucleobase head group of (+)-erythro-9-(2's-hydroxy-3's-nonyl)adenine [(+)-EHNA] as adenosine deaminase inhibitors.	Advinus Therapeutics
8100350	137	Cloned somatostatin receptors: identification of subtype-selective peptides and demonstration of high affinity binding of linear peptides.	University of Pennsylvania
17317569	7	High-throughput screening for human lysosomal beta-N-Acetyl hexosaminidase inhibitors acting as pharmacological chaperones.	Research Institute, Hospital For Sick Children