24 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
28197315	10	Affinity-Based Selectivity Profiling of an In-Class Selective Competitive Inhibitor of Acyl Protein Thioesterase 2.	University Of Michigan
28280261	84	Non-kinase targets of protein kinase inhibitors.	The University Of Sydney
26854376	31	Non-symmetrical furan-amidines as novel leads for the treatment of cancer and malaria.	University Of Manchester
23953689	37	Design, synthesis, biological and structural evaluation of functionalized resveratrol analogues as inhibitors of quinone reductase 2.	Purdue University
18400335	39	A novel quantitative structure-activity relationship method to predict the affinities of MT3 melatonin binding site.	Lanzhou University
22494098	8	Dabigatran and dabigatran ethyl ester: potent inhibitors of ribosyldihydronicotinamide dehydrogenase (NQO2).	Caprotec Bioanalytics
23131339	6	Synthesis of novel¿¿3 receptor ligands via an unusual Knoevenagel condensation.	Moscow State University
20684563	176	Discovery of N-{1-[3-(3-oxo-2,3-dihydrobenzo[1,4]oxazin-4-yl)propyl]piperidin-4-yl}-2-phenylacetamide (Lu AE51090): an allosteric muscarinic M1 receptor agonist with unprecedented selectivity and procognitive potential.	H. Lundbeck
20558073	28	Design, synthesis, and biological evaluation of resveratrol analogues as aromatase and quinone reductase 2 inhibitors for chemoprevention of cancer.	Purdue University
22206487	17	Design, synthesis, and biological evaluation of potent quinoline and pyrroloquinoline ammosamide analogues as inhibitors of quinone reductase 2.	Purdue University
21859103	21	Novel inhibitors of NRH:quinone oxidoreductase 2 (NQO2): crystal structures, biochemical activity, and intracellular effects of imidazoacridin-6-ones.	University Of Manchester
21105712	25	Potential chemopreventive agents based on the structure of the lead compound 2-bromo-1-hydroxyphenazine, isolated from Streptomyces species, strain CNS284.	Purdue University
21377769	30	Design and synthesis of naphthalenic derivatives as new ligands at the melatonin binding site MT3.	University Of Lille
21261296	6	Bioactive compounds from the fern Lepisorus contortus.	Yunnan Normal University
21074425	44	In silico identification and biochemical evaluation of novel inhibitors of NRH:quinone oxidoreductase 2 (NQO2).	University Of Manchester And Manchester Cancer Research Center
20356739	18	Imidazoacridin-6-ones as novel inhibitors of the quinone oxidoreductase NQO2.	The University Of Manchester And Manchester Cancer Research Center
20036559	31	Triazoloacridin-6-ones as novel inhibitors of the quinone oxidoreductases NQO1 and NQO2.	University Of Manchester And Manchester Cancer Research Center
12213062	70	Synthesis of a novel series of benzocycloalkene derivatives as melatonin receptor agonists.	Takeda Chemical Industries
11960497	36	Synthesis of nitroindole derivatives with high affinity and selectivity for melatoninergic binding sites MT(3).	Institut De Chimie Pharmaceutique Albert Lespagnol
9166718	19	Differential expression of multiple somatostatin receptors in the rat cerebellum during development.	Dynamique Des Systemes Neuroendocriniens
9163561	56	The putative 5-HT1A receptor antagonist DU125530 blocks the discriminative stimulus of the 5-HT1A receptor agonist flesinoxan in pigeons.	Cns-Pharmacology
8824284	43	Identification of a novel hypothalamic neuropeptide Y receptor associated with feeding behavior.	Bayer