43 results on '"Andrew K. Takle"'
Search Results
2. Supplementary Figure 3 from Demonstration of a Genetic Therapeutic Index for Tumors Expressing Oncogenic BRAF by the Kinase Inhibitor SB-590885
3. Supplementary Figure 1 from Demonstration of a Genetic Therapeutic Index for Tumors Expressing Oncogenic BRAF by the Kinase Inhibitor SB-590885
4. Data from Demonstration of a Genetic Therapeutic Index for Tumors Expressing Oncogenic BRAF by the Kinase Inhibitor SB-590885
5. Identification of pyrimidinyl piperazines as non-iminosugar glucocerebrosidase (GCase) pharmacological chaperones
6. Potent oxadiazole CGRP receptor antagonists for the potential treatment of migraine
7. The identification of potent, selective and CNS penetrant furan-based inhibitors of B-Raf kinase
8. Demonstration of a Genetic Therapeutic Index for Tumors Expressing Oncogenic BRAF by the Kinase Inhibitor SB-590885
9. (1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors
10. Collaborative approaches to anticancer drug discovery and development: a Cancer Research UK perspective
11. Pleuromutilins. Part 1 The identification of novel mutilin 14-carbamates
12. Preparation and reactivity of carbapenem-2-stannane
13. Chiral oxime ethers in asymmetric synthesis. Part 4. Asymmetric synthesis of N-protected amines and β-amino acids by the addition of organometallic reagents to ROPHy/SOPHy-derived aldoximes
14. Novel C-2 Substituted Carbapenem Derivatives. Part IV. Synthesis and Biological Activity of Five Membered Heteroaromatic Derivatives
15. Cycloadditions of Cephalosporins. A Comprehensive Study of the Reaction of Cephalosporin Triflates with Olefins, Acetylenes, and Dienes To Form [2 + 2] and [4 + 2] Adducts
16. Identification of clinical candidates from the benzazepine class of histamine H3 receptor antagonists
17. The discovery of the benzazepine class of histamine H3 receptor antagonists
18. O-(1-Phenylbutyl)benzyloxyacetaldoxime, a Versatile Reagent for the Asymmetric Synthesis of Protected 1,2-Aminoalcohols and 2-Hydroxymethyl Nitrogen Heterocycles
19. ChemInform Abstract: Cycloadditions of Cephalosporins. A General Synthesis of Novel 2,3- Fused Cyclobutane and Cyclobutene Cephems
20. ChemInform Abstract: Cycloadditions of Cephalosporins. The Formation (4 + 2) Adducts with 5- Membered Heterocycles
21. ChemInform Abstract: Novel C-2 Substituted Carbapenem Derivatives. Part 1. Synthesis and Biological Activity of Non-Aromatic Heterocyclic Derivatives
22. ChemInform Abstract: Chiral Oxime Ethers in Asymmetric Synthesis. Part 4. Asymmetric Synthesis of N-Protected Amines and β-Amino Acids by the Addition of Organometallic Reagents to ROPHy/SOPHy-Derived Aldoximes
23. ChemInform Abstract: Preparation and Reactivity of Carbapenem-2-stannane
24. Orally active C-6 heteroaryl- and heterocyclyl-substituted imidazo[1,2-a]pyridine acid pump antagonists (APAs)
25. Aryl sulphonyl amides as potent agonists of the growth hormone secretagogue (ghrelin) receptor
26. Potent achiral agonists of the growth hormone secretagogue (ghrelin) receptor. Part 2: Lead optimisation
27. Corrigendum to '(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors' [Bioorg. Med. Chem. Lett. 15 (2005) 3402–3406]
28. Pyridone derivatives as potent, orally bioavailable VLA-4 integrin antagonists
29. The Identification of Potent and Selective Imidazole-Based Inhibitors of B-Raf Kinase
30. The identification of potent and selective imidazole-based inhibitors of B-Raf kinase
31. Chiral oxime ethers in asymmetric synthesis. O-(1-Phenylbutyl)benzyloxyacetaldoxime, a versatile reagent for the asymmetric synthesis of protected 1,2-aminoalcohols, alpha-amino acid derivatives, and 2-hydroxymethyl nitrogen heterocycles including iminosugars
32. (1H-imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: further optimisation as highly potent and selective MSK-1-inhibitors
33. Asymmetric Synthesis of N-Protected Amino Acids by the Addition of Organolithium Carboxyl Synthons to ROPHy/SOPHy-Derived Aldoximes and Ketoximes
34. Asymmetric synthesis of N-protected amino acids by the addition of organolithium carboxyl synthons to ROPHy/SOPHy-derived aldoximes and ketoximes
35. 6-Aryl-pyrazolo[3,4-b]pyridines: Potent Inhibitors of Glycogen Synthase Kinase-3 (GSK-3)
36. 6-heteroaryl-pyrazolo[3,4-b]pyridines: potent and selective inhibitors of glycogen synthase kinase-3 (GSK-3)
37. O‐(1‐Phenylbutyl)benzyloxyacetaldoxime, a Versatile Reagent for the Asymmetric Synthesis of Protected 1,2‐Amino Alcohols and 2‐Hydroxymethyl Nitrogen Heterocycles
38. Novel C-2 substituted carbapenem derivatives. Part I. Synthesis and biological activity of non-aromatic heterocyclic derivatives
39. Corrigendum to 'Pyridone derivatives as potent and selective VLA-4 integrin antagonists' [Bioorg. Med. Chem. Lett. 16 (2006) 2256–2259]
40. Asymmetric synthesis of N-protected amino acids by the addition of organolithium carboxyl synthons to ROPHy/SOPHy-derived aldoximes and ketoximesChiral oxime ethers in asymmetric synthesis. Part 6.1
41. Cycloadditions of cephalosporins. The formation of [4+2] adducts with 5-membered heterocycles
42. Cycloadditions of cephalosporins. A general synthesis of novel 2,3-fused cyclobutane and cyclobutene cephems
43. Novel tricyclic pyrazole BRAF inhibitors with imidazole or furan central scaffolds
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.