24 articles for thisTarget

---

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

PMID	Data	Article Title	Organization
27783978	9	Recent discovery of non-nucleobase thymidine phosphorylase inhibitors targeting cancer.	Aimst University
24686016	22	Discovery of mixed type thymidine phosphorylase inhibitors endowed with antiangiogenic properties: synthesis, pharmacological evaluation and molecular docking study of 2-thioxo-pyrazolo[1,5-a][1,3,5]triazin-4-ones. Part II.	National University of Singapore
24177367	6	Fragment-based approach to the design of 5-chlorouracil-linked-pyrazolo[1,5-a][1,3,5]triazines as thymidine phosphorylase inhibitors.	National University of Singapore
24131420	33	Design of novel potent inhibitors of human uridine phosphorylase-1: synthesis, inhibition studies, thermodynamics, and in vitro influence on 5-fluorouracil cytotoxicity.	Pontifical Catholic University of Rio Grande Do Sul
23871912	36	A structure-activity relationship study of 1,2,4-triazolo[1,5-a][1,3,5]triazin-5,7-dione and its 5-thioxo analogues on anti-thymidine phosphorylase and associated anti-angiogenic activities.	National University of Singapore
23688695	1	Synthesis of pyrazolo[1,5-a][1,3,5]triazine derivatives as inhibitors of thymidine phosphorylase.	National University of Singapore
20053558	17	Structural diversity of nucleoside phosphonic acids as a key factor in the discovery of potent inhibitors of rat T-cell lymphoma thymidine phosphorylase.	Academy of Sciences of The Czech Republic
15658853	31	Aminoimidazolylmethyluracil analogues as potent inhibitors of thymidine phosphorylase and their bioreductive nitroimidazolyl prodrugs.	University of Manchester
14552762	12	Identification of a novel class of inhibitor of human and Escherichia coli thymidine phosphorylase by in silico screening.	University of Manchester
12467627	7	Design of novel N-(2,4-dioxo-1,2,3,4-tetrahydro-thieno[3,2-d]pyrimidin-7-yl)-guanidines as thymidine phosphorylase inhibitors, and flexible docking to a homology model.	Attenuon
21195612	5	8-Aza-7,9-dideazaxanthine acyclic nucleoside phosphonate inhibitors of thymidine phosphorylase.	Academy of Sciences of The Czech Republic
20138520	1	The role of phosphate in the action of thymidine phosphorylase inhibitors: Implications for the catalytic mechanism.	University At Buffalo
17870212	7	Xanthine oxidase-activated prodrugs of thymidine phosphorylase inhibitors.	The University of Manchester
17181163	6	Synthesis and evaluation of multisubstrate bicyclic pyrimidine nucleoside inhibitors of human thymidine phosphorylase.	Attenuon
16942029	22	5'-O-tritylinosine and analogues as allosteric inhibitors of human thymidine phosphorylase.	Instituto De QuíMica MéDica (Csic)
12519058	8	Potential tumor-selective nitroimidazolylmethyluracil prodrug derivatives: inhibitors of the angiogenic enzyme thymidine phosphorylase.	University of Manchester
12182865	88	Structure-activity relationship of biaryl acylsulfonamide analogues on the human EP(3) prostanoid receptor.	Merck Frosst Centre For Therapeutic Research
10891120	7	Novel nonsubstrate inhibitors of human thymidine phosphorylase, a potential target for tumor-dependent angiogenesis.	Istituto Di Genetica Biochimica Ed Evoluzionistica
30615449	24	Design of Novel Inhibitors of Human Thymidine Phosphorylase: Synthesis, Enzyme Inhibition, in Vitro Toxicity, and Impact on Human Glioblastoma Cancer.	Universidade Federal Do Pampa
29046238	17	1,3,5-Triazines: A promising scaffold for anticancer drugs development.	Universit£
29247859	26	Synthesis and biological evaluation of novel 1-(aryl-aldehyde-oxime)uracil derivatives as a new class of thymidine phosphorylase inhibitors.	Yunnan University
29853339	22	Rational design of bis-indolylmethane-oxadiazole hybrids as inhibitors of thymidine phosphorylase.	Imam Abdulrahman Bin Faisal University
16039528	16	Defining Cdk5 ligand chemical space with small molecule inhibitors of tau phosphorylation.	Harvard Medical School
15664518	4	Enhanced ligand affinity for receptors in which components of the binding site are independently mobile.	University of Sheffield