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Fmoc-L-trans-Hyp(Ph)-OH
Nombre químico: (2S,4R)-1-(9-Fluorenylmethyloxycarbonyl)-4-phenoxy-pyrrolidine-2-carboxylic acid // Sinónimos: (2S,4R)-Fmoc-4-phenoxyl-pyrrolidine-2-carboxylic acid, (2S,4R)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)-4-phenoxypyrrolidine-2-carboxylic acid, Fmoc-L-Pro(4-OPh)-OH (2S,4R),Fmoc-L-Hyp(Ph)-OH, Fmoc-Hyp( Ph)-OH, Fmoc-L-Hyp(Ph)-OH (2S,4R), Fmoc-cis-Hyp(Ph
- Nº Artículo:FAA5210
- Nº CAS:1313390-76-9
- Fórmula:C26H23NO5
- Storage temperature:2-8°C
- Masa molecular:429,46 g/mol
from 450,00 €
description
Discovery of Potent Antagonists of the Antiapoptotic Protein XIAP for the Treatment of Cancer. Thorsten K. Oost, Chaohong Sun, Robert C. Armstrong, Ali-Samer Al-Assaad, Stephen F. Betz, Thomas L. Deckwerth, Hong Ding, Steven W. Elmore, Robert P. Meadows, Edward T. Olejniczak, Andrew Oleksijew, Tilman Oltersdorf, Saul H. Rosenberg, Alexander R. Shoemaker, Kevin J. Tomaselli, Hua Zou, Stephen W. Fesik; J. Med. Chem. 2004; 47(18): 4417-4426. DOI: 10.1021/jm040037k
Large ring-forming alkylations provide facile access to composite macrocycles. Tristan E. Rose , Kenneth V. Lawson, Patrick. G. Harran; Chem. Sci. 2015; 6: 2219-2223. DOI: 10.1039/C4SC03848G
The Outcomes of Decorated Prolines in the Discovery of Antimicrobial Peptides from Temporin‐L. Elisabetta Buommino, Alfonso Carotenuto, Ignazio Antignano, Rosa Bellavita, Bruno Casciaro, Maria Rosa Loffredo, Francesco Merlino, Ettore Novellino, Maria Luisa Mangoni, Francesca Paola Nocera, Diego Brancaccio, Pasqualina Punzi, Daniela Roversi, Raffaele Ingenito, Elisabetta Bianchi, Paolo Grieco; ChemMedChem 2019; 14: 1283-1290. DOI: 10.1002/cmdc.201900221
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All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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