49 results on '"McKittrick B"'
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2. The discovery of potent, selectivity, and orally bioavailable pyrozoloquinolines as PDE10 inhibitors for the treatment of Schizophrenia
3. ChemInform Abstract: Condensation of Ethyl Mandelate with a Cinnamate Ester: Bicyclocarbolactone Formation.
4. ChemInform Abstract: Design and Synthesis of Phosphinic Acids That Triply Inhibit Endothelin Converting Enzyme, Angiotensin Converting Enzyme and Neutral Endopeptidase 24.11.
5. ChemInform Abstract: Highly Potent and Selective Inhibitors of Endothelin Converting Enzyme.
6. ChemInform Abstract: Synthesis of C3 Heteroatom-Substituted Azetidinones That Display Potent Cholesterol Absorption Inhibitory Activity.
7. Crystal structure of catalytic domain of TACE with hydroxamate inhibitor
8. Hepatitis C virus NS3-4A serine protease inhibitors: SAR of moiety with improved potency
9. Hepatitis C virus NS3-4A serine protease inhibitors: SAR of [formula omitted] moiety with improved potency
10. ChemInform Abstract: The Gif System as a Tool in Medicinal Chemistry: The Oxidation of Sch 57726 Under GoAggIII Conditions.
11. ChemInform Abstract: Stereoselective Synthesis and Biological Activity of cis‐Azetidinones as Cholesterol Absorption Inhibitors.
12. ChemInform Abstract: Synthetic Entries to 6‐Fluoro‐7‐substituted Indole Derivatives.
13. FERRY: access control and quota management service
14. Design and synthesis of phosphinic acids that triply inhibit endothelin converting enzyme, angiotensin converting enzyme and neutral endopeptidase 24.11
15. Highly potent and selective inhibitors of endothelin converting enzyme
16. Synthesis of C3 Heteroatom-Substituted Azetidinones That Display Potent Cholesterol Absorption Inhibitory Activity
17. Potent Tetracyclic Guanine Inhibitors of PDE1 and PDE5 Cyclic Guanosine Monophosphate Phosphodiesterases with Oral Antihypertensive Activity
18. The Gif system as a tool in medicinal chemistry: the oxidation of Sch 57726 under GoAgg^I^I^I conditions
19. Stereoselective synthesis and biological activity of cis azetidinones as cholesterol absorption inhibitors
20. ChemInform Abstract: A SIMPLE SYNTHESIS OF THE NATURAL BENZOFURANOQUINONE, ACAMELIN
21. ChemInform Abstract: Advances in the Chemistry of 2,3‐Epoxy Alcohols. New Methodology for Contra‐ Trans‐Diaxial Opening and Selective Enediol Oxidation.
22. ChemInform Abstract: NATURAL BENZOFURANS: SYNTHESIS OF THE ARYLBENZOFURAN CONSTITUENTS OF SOPHORA TOMENTOSA
23. ChemInform Abstract: syn‐Stereoselective Epoxidation of Allylic Ethers Using CF3CO3H.
24. ChemInform Abstract: NATURAL BENZOFURANS. SYNTHESIS OF EUPOMATENOIDS‐1, ‐3, ‐4, ‐5, ‐6, ‐7, AND ‐13
25. ChemInform Abstract: SYNTHESIS OF THE YEAST ANTIOXIDANT BENZOFURAN AND ANALOGS
26. BOOK AND FILM REVIEWS: A PSSC Problem Book: Guided Assignments in PSSC Physics
27. Synthesis of a γ-Secretase Inhibitor.
28. ChemInform Abstract: Synthesis of C3 Heteroatom-Substituted Azetidinones That Display Potent Cholesterol Absorption Inhibitory Activity.
29. ChemInform Abstract: Design and Synthesis of Phosphinic Acids That Triply Inhibit Endothelin Converting Enzyme, Angiotensin Converting Enzyme and Neutral Endopeptidase 24.11.
30. ChemInform Abstract: Highly Potent and Selective Inhibitors of Endothelin Converting Enzyme.
31. ChemInform Abstract: Condensation of Ethyl Mandelate with a Cinnamate Ester: Bicyclocarbolactone Formation.
32. History and Prospects of Drug Discovery and Development Collaboration between Industry and Academia.
33. Peptide Nucleic Acids Containing Cationic/Amino-Alkyl Modified Bases Promote Enhanced Hybridization Kinetics and Thermodynamics with Single-Strand DNA.
34. Generation of Leads for γ-Secretase Modulation.
35. Discovery of potent iminoheterocycle BACE1 inhibitors.
36. The discovery of potent, selective, and orally active pyrazoloquinolines as PDE10A inhibitors for the treatment of Schizophrenia.
37. Discovery of SCH 900271, a Potent Nicotinic Acid Receptor Agonist for the Treatment of Dyslipidemia.
38. Discovery of a potent thiadiazole class of histamine h3 receptor antagonist for the treatment of diabetes.
39. Discovery of a series of potent arylthiadiazole H(3) antagonists.
40. Iminoheterocycles as gamma-secretase modulators.
41. Structure and activity relationships of tartrate-based TACE inhibitors.
42. Discovery of Dinaciclib (SCH 727965): A Potent and Selective Inhibitor of Cyclin-Dependent Kinases.
43. Design and synthesis of tricyclic sulfones as gamma-secretase inhibitors with greatly reduced Notch toxicity.
44. The discovery of novel tartrate-based TNF-alpha converting enzyme (TACE) inhibitors.
45. Discovery and SAR of cyclic isothioureas as novel NPY Y1 receptor antagonists.
46. Design and discovery of 1,3-benzodiazepines as novel dopamine antagonists.
47. Discovery of novel hydroxamates as highly potent tumor necrosis factor-alpha converting enzyme inhibitors. Part II: optimization of the S3' pocket.
48. Discovery of novel hydroxamates as highly potent tumor necrosis factor-alpha converting enzyme inhibitors: Part I--discovery of two binding modes.
49. Pyrazolo[1,5-a]pyrimidines as orally available inhibitors of cyclin-dependent kinase 2.
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