3-[2-Amino-2-imidazolin-4(5)-yl]alanine (enduracididine) and 2-[2-amino-2-imidazolin-4(5)-yl] acetic acid in seeds of Lonchocarpus sericeus
✍ Scribed by Linda E. Fellows; Robert C. Hider; E.Arthur Bell
- Book ID
- 107841890
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- English
- Weight
- 321 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0031-9422
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
In the title compound, C 19 H 17 O 3 N 4 S, a substituted oxadiazole derivative and an important biologically active compound, electron delocalization in the oxadiazole ring is reflected in the C-N bond lengths.
The title compound, C~17~H~13~BrO~3~S, was prepared by alkaline hydrolysis of ethyl 2-[5-(4-bromophenyl)-3-methylsulfanyl-1-benzofuran-2-yl]acetate. There are two symmetry-independent molecules in the asymmetric unit. The 4-bromophenyl rings are rotated out of the benzofuran planes, with dihedral an
## Abstract magnified image The paper describes synthesis and antituberculosis activity of α‐[5‐(5‐amino‐1,3,4‐thiadiazol‐2‐yl)‐imidazol‐2‐ylthio]acetic acids (**5a,b**). The compounds were tested against __Mycobacterium tuberculosis__ strain H37Rv in comparison to rifampicin. Compounds exhibited