37 articles for thisTarget

---

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

PMID	Data	Article Title	Organization
26260335	14	Tight binding enantiomers of pre-clinical drug candidates.	Victoria University Of Wellington
31484	4	Stereoelectronic factors in the binding of substrate analogues and inhibitors to purine nucleoside phosphorylase isolated from human erythrocytes.	TBA
22264015	29	N-phosphonocarbonylpyrrolidine derivatives of guanine: a new class of bi-substrate inhibitors of human purine nucleoside phosphorylase.	Academy Of Sciences Of The Czech Republic
19386496	3	Synthesis of analogs of forodesine HCl, a human purine nucleoside phosphorylase inhibitor-Part II.	Biocryst Pharmaceuticals
19170524	38	Third-generation immucillins: syntheses and bioactivities of acyclic immucillin inhibitors of human purine nucleoside phosphorylase.	Industrial Research
18778937	15	Immucillins in custom catalytic-site cavities.	Albert Einstein College Of Medicine Of Yeshiva University
17004717	22	Simplified analogues of immucillin-G retain potent human purine nucleoside phosphorylase inhibitory activity.	Universit£
15163207	27	Targeting the polyamine pathway with transition-state analogue inhibitors of 5'-methylthioadenosine phosphorylase.	Industrial Research
14613329	11	Synthesis of second-generation transition state analogues of human purine nucleoside phosphorylase.	Industrial Research
12852771	26	Exploring structure-activity relationships of transition state analogues of human purine nucleoside phosphorylase.	Industrial Research
8478902	18	Nucleosides. 5. Synthesis of guanine and formycin B derivatives as potential inhibitors of purine nucleoside phosphorylase.	National Defense Medical Center
8254607	36	Structure-based design of inhibitors of purine nucleoside phosphorylase. 3. 9-Arylmethyl derivatives of 9-deazaguanine substituted on the methylene group.	Biocryst Pharmaceuticals
1578487	12	Inhibitors of human purine nucleoside phosphorylase. Synthesis of pyrrolo[3,2-d]pyrimidines, a new class of purine nucleoside phosphorylase inhibitors as potentially T-cell selective immunosuppressive agents. Description of 2,6-diamino-3,5-dihydro-7-(3-thienylmethyl)-4H-pyrrolo[3,2-d] pyrimidin-4-o	Warner-Lambert
1573639	17	Inhibitors of human purine nucleoside phosphorylase. Synthesis and biological activities of 8-amino-3-benzylhypoxanthine and related analogues.	Warner-Lambert
3123692	6	Synthesis and evaluation of 5-amino-1-beta-D-ribofuranosyl-1,2,4-triazole-3-carboxamidine and certain related nucleosides as inhibitors of purine nucleoside phosphorylase.	Nucleic Acid Research Institute
3091835	3	Inhibitors of human purine nucleoside phosphorylase. Synthesis, purine nucleoside phosphorylase inhibition, and T-cell cytotoxicity of 2,5-diaminothiazolo[5,4-d]pyrimidin-7(6H)-one and 2,5-diaminothiazolo[4,5-d]pyrimidin-7(6H)-one. Two thio isosteres of 8-aminoguanine.	TBA
3093681	7	Synthesis of 8-amino-3-deazaguanine via imidazole precursors. Antitumor activity and inhibition of purine nucleoside phosphorylase.	TBA
11959007	27	Benzimidazole-4,7-diones as inhibitors of protozoal (Toxoplasma gondii) purine nucleoside phosphorylase.	Universit£
	19	Phosphonate derivatives of N9-benzylguanine: a new class of potent purine nucleoside phosphorylase inhibitors	TBA
20817362	25	Exploring new inhibitors of Plasmodium falciparum purine nucleoside phosphorylase.	Instituto De ParasitologíA Y Biomedicina LóPez-Neyra
19620996	2	Enzymatic transition states and dynamic motion in barrier crossing.	Albert Einstein College Of Medicine
20189401	24	Structural-based design and synthesis of novel 9-deazaguanine derivatives having a phosphate mimic as multi-substrate analogue inhibitors for mammalian PNPs.	Tokyo University Of Pharmacy And Life Sciences
20129792	10	Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies.	Universidade Federal Da Bahia
19386498	3	Synthesis of analogs of forodesine HCl, a human purine nucleoside phosphorylase inhibitor-Part I.	Biocryst Pharmaceuticals
18800772	18	A beta-fluoroamine inhibitor of purine nucleoside phosphorylase.	Industrial Research
17544667	10	Synthesis and biological evaluation of 9-deazaguanine derivatives connected by a linker to difluoromethylene phosphonic acid as multi-substrate analogue inhibitors of PNP.	Tokyo University Of Pharmacy And Life Sciences
12502369	8	8-Aza-immucillins as transition-state analogue inhibitors of purine nucleoside phosphorylase and nucleoside hydrolases.	Industrial Research
10522701	14	Synthesis and biological evaluation of 1,1-difluoro-2-(tetrahydro-3-furanyl)ethylphosphonic acids possessing a N9-purinylmethyl functional group at the ring. a new class of inhibitors for purine nucleoside phosphorylases.	Tokyo University Of Pharmacy & Life Science
8632418	21	Guanine, pyrazolo[3,4-d]pyrimidine, and triazolo[4,5-d]pyrimidine (8-azaguanine) phosphonate acyclic derivatives as inhibitors of purine nucleoside phosphorylase.	Burroughs Wellcome
8421291	73	Structure-based design of inhibitors of purine nucleoside phosphorylase. 1. 9-(arylmethyl) derivatives of 9-deazaguanine.	Biocryst Pharmaceuticals
8230137	14	9-[(Phosphonoalkyl)benzyl]guanines. Multisubstrate analogue inhibitors of human erythrocyte purine nucleoside phosphorylase.	Burroughs Wellcome
8164252	18	Structure-based design of inhibitors of purine nucleoside phosphorylase. 4. A study of phosphate mimics.	Ciba-Geigy
7699692	14	[[(Guaninylalkyl)phosphinico]methyl]phosphonic acids. Multisubstrate analogue inhibitors of human erythrocyte purine nucleoside phosphorylase.	Burroughs Wellcome