16 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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New 5H-pyridazino[4,5-b]indole derivatives. Synthesis and studies as inhibitors of blood platelet aggregation and inotropics.

Universidad De Navarra
Novel sulfonylurea derivatives as H3 receptor antagonists. Preliminary SAR studies.

Universidad De Navarra
Novel antagonists of 5-HT3 receptors. Synthesis and biological evaluation of piperazinylquinoxaline derivatives.

Universidad De Navarra
Building a MCHR1 homology model provides insight into the receptor-antagonist contacts that are important for the development of new anti-obesity agents.

Universidad De Navarra
Synthesis and anti-inflammatory/antioxidant activities of some new ring substituted 3-phenyl-1-(1,4-di-N-oxide quinoxalin-2-yl)-2-propen-1-one derivatives and of their 4,5-dihydro-(1H)-pyrazole analogues.

Universidad De Navarra
The role of imidazole and benzimidazole heterocycles in Chagas disease: A review.

Universidad De Navarra
Examination of multiple Trypanosoma cruzi targets in a new drug discovery approach for Chagas disease.

Universidad De Navarra
Synthesis of new thiophene and benzo[b]thiophene hydrazide derivatives as human NPY Y(5) antagonists.

Universidad De Navarra
Synthesis and molecular modeling of new 1-aryl-3-[4-arylpiperazin-1-yl]-1-propane derivatives with high affinity at the serotonin transporter and at 5-HT(1A) receptors.

Universidad De Navarra
In Vitro and in Vivo Anti-Trypanosoma cruzi Activity of New Arylamine Mannich Base-Type Derivatives.

Universidad De Navarra
New 1-aryl-3-(4-arylpiperazin-1-yl)propane derivatives, with dual action at 5-HT1A serotonin receptors and serotonin transporter, as a new class of antidepressants.

Universidad De Navarra
Rational modification of Mannich base-type derivatives as novel antichagasic compounds: Synthesis, in vitro and in vivo evaluation.

Universidad De Navarra
Development and Therapeutic Potential of Selenazo Compounds.

Universidad De Navarra
Structure-activity relationship of new antimalarial 1-aryl-3-susbtituted propanol derivatives: Synthesis, preliminary toxicity profiling, parasite life cycle stage studies, target exploration, and targeted delivery.

Universidad De Navarra
Phenotypic Screening To Discover Novel Chemical Series as Efficient Antihemorrhagic Agents.

Universidad De Navarra
A major role for a set of non-active site mutations in the development of HIV-1 protease drug resistance.

The Johns Hopkins University