22 results on '"Ohkubo, Mitsuru"'
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2. Orally available pyridinylpyrimidine derivatives as novel RANKL-induced osteoclastogenesis inhibitors
3. Isoxazolopyridone derivatives as allosteric metabotropic glutamate receptor 7 antagonists
4. Solid-phase synthesis of aryl, heteroaryl, and sterically hindered alkyl amines using the Curtius rearrangement
5. Discovery of potent and selective PARP-1 and PARP-2 inhibitors: SBDD analysis via a combination of X-ray structural study and homology modeling
6. Design, synthesis, and structure–activity relationships of potent GPIIb/IIIa antagonists: discovery of FK419
7. An efficient synthesis of the orally-active GpIIb/IIIa antagonist FR184764
8. Development of an orexin-2 receptor selective agonist, [Ala11, d-Leu15]orexin-B
9. A new class of type I protein geranylgeranyltransferase (GGTase I) inhibitor
10. Synthesis and biological activities of NB-506 analogues modified at the glucose group
11. Synthesis and biological activities of NB-506 analogues: Effects of the positions of two hydroxyl groups at the indole rings
12. Synthesis and biological activities of topoisomerase I inhibitors, 6-N-amino analogues of NB-506
13. Solid phase synthesis of aryl and heteroaryl amines using the Curtius rearrangement
14. Synthesis of Dissymmetric Indolocarbazole Glycosides Using the Mitsunobu Reaction at the Glycosylation Step
15. Synthesis of NB-506, A new anticancer agent
16. Design, synthesis, and evaluation of fibrinogen inhibitors, ω-(p-amidinophenoxy) alkanoylaspartic acid derivatives
17. Practical synthesis of indolopyrrolocarbazoles
18. Neurochemical and electrophysiological studies on FR115427, a novel non-competitive NMDA receptor antagonist
19. Total synthesis of a new topoisomerase II inhibitor BE 10988
20. Natural products syntheses using anodic oxidation of phenols as a key step
21. An efficient enantioselective preparation of 2-substituted-3-hydroxypropionic acids via chemo-enzymatic reaction
22. Synthesis of (±)-silphinene using electrochemical method as a key step
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