Synthesis and Taste Properties of 4,1′,4′,6′-Tetrahalodeoxysucrose Analogues.
✍ Scribed by A. S. Md. Sofian; C. Kuan Lee
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 203 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract A variety of 4‐substituted quinolin‐2(1__H__)‐ones were prepared and evaluated for __N__‐methyl‐D‐aspar‐tate (NMDA) receptor binding site activity and their abilities to inhibit neurotoxicity. The 4‐(2‐car‐bethoxyethanamino)‐7‐chloro‐3‐nitroquinolin‐2(1__H__)‐one (**9b**) exhibited favo
myo-Inositol 1,4,6-u-&phosphate, in optically inactive and active forms, was prepared in order to compare its biological activity with that of myo-inositol 1,3,4,6-tetrakisphosphate which releases Ca2+ from an intracellular store.