25 results on '"Zhang, Yanan"'
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2. Discovery of Arylsulfonamides as Dual Orexin Receptor Agonists
3. Development of pH/Glutathione-Responsive Theranostic Agents Activated by Glutathione S-Transferase π for Human Colon Cancer
4. Neuropeptide FF and Its Receptors: Therapeutic Applications and Ligand Development
5. Synthesis and Pharmacological Evaluation of 1-Phenyl-3-Thiophenylurea Derivatives as Cannabinoid Type-1 Receptor Allosteric Modulators
6. Development of 3-(4-Chlorophenyl)-1-(phenethyl)urea Analogues as Allosteric Modulators of the Cannabinoid Type-1 Receptor: RTICBM-189 is Brain Penetrant and Attenuates Reinstatement of Cocaine-Seeking Behavior
7. Blocking Alcoholic Steatosis in Mice with a Peripherally Restricted Purine Antagonist of the Type 1 Cannabinoid Receptor
8. Novel Diarylurea Based Allosteric Modulators of the Cannabinoid CB1 Receptor: Evaluation of Importance of 6-Pyrrolidinylpyridinyl Substitution
9. Novel Diarylurea Based Allosteric Modulators of the Cannabinoid CB1 Receptor: Evaluation of Importance of 6-Pyrrolidinylpyridinyl Substitution
10. Novel β-Carboline/Hydroxamic Acid Hybrids Targeting Both Histone Deacetylase and DNA Display High Anticancer Activity via Regulation of the p53 Signaling Pathway
11. Diarylureas as Allosteric Modulators of the Cannabinoid CB1 Receptor: Structure–Activity Relationship Studies on 1-(4-Chlorophenyl)-3-{3-[6-(pyrrolidin-1-yl)pyridin-2-yl]phenyl}urea (PSNCBAM-1)
12. Identification of N-[(5-{[(4-Methylphenyl)sulfonyl]amino}-3-(trifluoroacetyl)-1H-indol-1-yl)acetyl]-l-leucine (NTRC-824), a Neurotensin-like Nonpeptide Compound Selective for the Neurotensin Receptor Type 2
13. Identification of 1-({[1-(4-Fluorophenyl)-5-(2-methoxyphenyl)-1H-pyrazol-3-yl]carbonyl}amino)cyclohexane Carboxylic Acid as a Selective Nonpeptide Neurotensin Receptor Type 2 Compound
14. Peripherally Selective Diphenyl Purine Antagonist of the CB1 Receptor
15. Substituted Tetrahydroisoquinolines as Selective Antagonists for the Orexin 1 Receptor
16. Diphenyl Purine Derivatives as Peripherally Selective Cannabinoid Receptor 1 Antagonists
17. Design and Synthesis of Cannabinoid Receptor 1 Antagonists for Peripheral Selectivity
18. Synthesis and Biological Evaluation of Bivalent Ligands for the Cannabinoid 1 Receptor
19. Conformationally Constrained Analogues of N-(Piperidinyl)-5-(4-Chlorophenyl)-1-(2,4- Dichlorophenyl)-4-Methyl-1H-Pyrazole-3-Carboxamide (SR141716): Design, Synthesis, Computational Analysis, And Biological Evaluations
20. Diarylureas as AllostericModulators of the CannabinoidCB1 Receptor: Structure–Activity Relationship Studies on 1-(4-Chlorophenyl)-3-{3-[6-(pyrrolidin-1-yl)pyridin-2-yl]phenyl}urea(PSNCBAM-1).
21. Identification of N-[(5-{[(4-Methylphenyl)sulfonyl]amino}-3-(trifluoroacetyl)-1H-indol-1-yl)acetyl]-l-leucine(NTRC-824), a Neurotensin-like Nonpeptide Compound Selective for theNeurotensin Receptor Type 2.
22. Peripherally Selective DiphenylPurine Antagonistof the CB1 Receptor.
23. SubstitutedTetrahydroisoquinolines as Selective Antagonistsfor the Orexin 1 Receptor.
24. Diphenyl Purine Derivativesas Peripherally SelectiveCannabinoid Receptor 1 Antagonists.
25. Design and Synthesis ofCannabinoid Receptor 1 Antagonists for Peripheral Selectivity.
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