✦ LIBER ✦

Application of a conformationally restricted Phe-Leu dipeptide mimetic to the design of a combined inhibitor of angiotensin I-converting enzyme and neutral endopeptidase 24.11

✍ Scribed by Flynn, Gary A.; Beight, Douglas W.; Mehdi, Shujaath; Koehl, Jack R.; Giroux, Eugene L.; French, John F.; Hake, Paul W.; Dage, Richard C.

Book ID: 115518270
Publisher: American Chemical Society
Year: 1993
Tongue: English
Weight: 568 KB
Volume: 36
Category: Article
ISSN: 0022-2623
DOI: 10.1021/jm00068a022

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Design and synthesis of a new class of c

Design and synthesis of a new class of conformationally constrained inhibitors to probe the active sites of thermolysine and neutral endopeptidase 24.11

✍ Eric Fillion; Denis Gravel 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 310 KB

The design as well as the synthesis, resolution, and biological evaluation of the neutral endopeptidase 24.11 inhibitors, (1S,2R,5S)-(-)-[(2-mercapto-5-phenyl-cyclopentanecarbonyl)amino]-acetic acid and (1R,2S,5R)-(+)- [(2-mercapto-5-phenyl-cyclopentanecarbonyl)-amino]-acetic acid are described.

ChemInform Abstract: Design and Synthesi

ChemInform Abstract: Design and Synthesis of a New Class of Conformationally Constrained Inhibitors to Probe the Active Sites of Thermolysine and Neutral Endopeptidase 24.11.

✍ E. FILLION; D. GRAVEL 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB