39 results on '"Nchinda, Aloysius"'
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2. Correction to “Identification of 2,4-Disubstituted Imidazopyridines as Hemozoin Formation Inhibitors with Fast-Killing Kinetics and In Vivo Efficacy in the Plasmodium falciparum NSG Mouse Model”
3. Identification of 2,4-Disubstituted Imidazopyridines as Hemozoin Formation Inhibitors with Fast-Killing Kinetics and In Vivo Efficacy in the Plasmodium falciparum NSG Mouse Model
4. Synthesis, Structure–Activity Relationship, and Mechanistic Studies of Aminoquinazolinones Displaying Antimycobacterial Activity
5. Lerisetron Analogues with Antimalarial Properties: Synthesis, Structure–Activity Relationship Studies, and Biological Assessment
6. Erratum for Brunschwig et al., “UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria”
7. Antimalarial Lead-Optimization Studies on a 2,6-Imidazopyridine Series within a Constrained Chemical Space To Circumvent Atypical Dose–Response Curves against Multidrug Resistant Parasite Strains
8. UCT943, a Next-Generation Plasmodium falciparum PI4K Inhibitor Preclinical Candidate for the Treatment of Malaria
9. Identification of Fast-Acting 2,6-Disubstituted Imidazopyridines That Are Efficacious in the in Vivo Humanized Plasmodium falciparum NODscidIL2Rγnull Mouse Model of Malaria
10. Novel Antitubercular 6-Dialkylaminopyrimidine Carboxamides from Phenotypic Whole-Cell High Throughput Screening of a SoftFocus Library: Structure–Activity Relationship and Target Identification Studies
11. Identification of a Potential Antimalarial Drug Candidate from a Series of 2-Aminopyrazines by Optimization of Aqueous Solubility and Potency across the Parasite Life Cycle
12. Medicinal Chemistry Optimization of Antiplasmodial Imidazopyridazine Hits from High Throughput Screening of a SoftFocus Kinase Library: Part 1
13. 2,4-Diaminothienopyrimidines as Orally Active Antimalarial Agents
14. Structure–Activity-Relationship Studies around the 2-Amino Group and Pyridine Core of Antimalarial 3,5-Diarylaminopyridines Lead to a Novel Series of Pyrazine Analogues with Oral in Vivo Activity
15. Structure–Activity Relationship Studies of Orally Active Antimalarial 3,5-Substituted 2-Aminopyridines
16. Characterization of angiotensin I-converting enzyme N-domain selectivity using positional-scanning combinatorial libraries of fluorescence resonance energy transfer peptides
17. 3,5-Diaryl-2-aminopyridines as a Novel Class of Orally Active Antimalarials Demonstrating Single Dose Cure in Mice and Clinical Candidate Potential
18. Novel Orally Active Antimalarial Thiazoles
19. Catalytic properties of recombinant dipeptidyl carboxypeptidase from Escherichia coli: a comparative study with angiotensin I-converting enzyme
20. Residue L143 of the Foot-and-Mouth Disease Virus Leader Proteinase Is a Determinant of Cleavage Specificity
21. Development of Domain‐Selective Angiotensin I‐Converting Enzyme Inhibitors
22. Synthesis and molecular modeling of a lisinopril–tryptophan analogue inhibitor of angiotensin I-converting enzyme
23. Synthesis of novel keto-ACE analogues as domain-selective angiotensin I-converting enzyme inhibitors
24. Crystal Structure of the N Domain of Human Somatic Angiotensin I-converting Enzyme Provides a Structural Basis for Domain-specific Inhibitor Design
25. Novel ketomethylene inhibitors of angiotensin I-converting enzyme (ACE): inhibition and molecular modelling
26. Development of Domain‐Selective Angiotensin I‐Converting Enzyme Inhibitors
27. Positional-Scanning Combinatorial Libraries of Fluorescence Resonance Energy Transfer Peptides for Defining Substrate Specificity of the Angiotensin I-Converting Enzyme and Development of Selective C-Domain Substrates
28. Novel Heterocyclic Analogues of the HIV‐1 Protease Inhibitor, Ritonavir.
29. Chromone Studies. Part 15. Formation and Condensation of Baylis—Hillman Adducts in DABCO‐Catalyzed Reactions of Chromone‐3‐carbaldehydes with Acrylonitrile.
30. Chromone studies. Part 15. Formation and condensation of Baylis–Hillman adducts in DABCO-catalysed reactions of chromone-3-carbaldehydes with acrylonitrile
31. Novel Heterocyclic Analogues of the HIV‐1 Protease Inhibitor, Ritonavir
32. Chromone Studies. Part 14. Unprecedented Dimerization of Chromone-3-carbaldehyde-Derived Baylis—Hillman Adducts.
33. Chromone Studies. Part 13. Synthesis and Electron-Impact Mass Spectrometric Studies of 5-Hydroxy-2-isopropyl-7-methoxychromone, a Constituent of the Medicinal Plant Baeckea frutescens, and Side-Chain Analogues
34. Chromone studies. Part 14. Unprecedented dimerisation of chromone-3-carbaldehyde-derived Baylis-Hillman adducts
35. Chromone Studies. Part 14.1 Unprecedented Dimerisation of Chromone-3-Carbaldehyde-Derived Baylis–Hillman Adducts
36. Chromone Studies. Part 11. Synthesis and Electron-Impact Mass Spectrometric Study of Granulosin and Side-Chain Analogues.
37. Chromone Studies. Part 11.1 Synthesis and Electron-Impact Mass Spectrometric Study of Granulosin and Side-Chain Analogues
38. ChemInform Abstract: Chromones Studies. Part 10. Substituent Effects on the Basicity of 2-(N,N-Dimethylamino)chromones.
39. Chromone studies. Part 10.1 Substituent effects on the basicity of 2-(N,N-dimethylamino)chromones
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