Poly(His-Asp-Ser-Gly) was synthesized from the fully protected tetrapeptide active ester hydrochloride, which was prepared by stepwise coupling, using pentachlorophenyl ester and mixed anhydride methods. Complete deprotection of the protected tetrapeptide polymer was achieved by using 90% trifluoroa
Studies of enzyme active sites: Synthesis and catalytic properties of L-histidylglycyl-L-aspartyl-L-seryl-L-phenylalanine
β Scribed by A. Kapoor; Soon M. Kang; Mary Ann Trimboli
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- English
- Weight
- 209 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The L-D-D tripeptide
A number of structural analogs of the antitumor compound, L-canavanine, [L-2-amino-4-(guanidinooxy)butyric acid], a Ξ΄-oxa analog of L-arginine, have been synthesized and their growth-inhibitory effects evaluated in cultured MIA-PaCa-2 pancreatic carcinoma cells by the 3-(4,5-dimethylthiazol-2-yl)-2,
A number of congeners of the antitumor compound L-canaline, [L-2-amino-4-(aminooxy)butyric acid], a structural analog of L-ornithine, have been synthesized and their growth-inhibitory effects evaluated in cultured MIA-PaCa-2 cells, a human pancreatic adenosarcoma, by the 3-(4,5-dimethylthiazol-2-yl)