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Fmoc-L-Pro(4-NH-Alloc)-OH (2S,4S)
Nombre químico: (2S,4S)-4-Allyloxycarbonylamino-1-(9-fluorenylmethyloxycarbonyl)-pyrrolidine-2-carboxylic acid // Sinónimos: (4S)-4-Allyloxycarbonylamino-1-(9-fluorenylmethyloxycarbonyl)-L-proline, Fmoc-Pro(4-NH-Alloc)-OH (2S,4S), Fmoc-Pro(4-NH-Aloc)-OH, Fmoc-L-Pro(4-NH-Aloc)-OH
- Nº Artículo:FAA3175
- Nº CAS:274676-10-7
- Fórmula:C24H24N2O6
- Storage temperature:2-8°C
- Masa molecular:436,46 g/mol
- Pureza:min. 99%
- Pureza Enantiomérica:min. 99,7%
from 85,00 €
description
The proximity of the amine and carboxylic acid enforced by the pyrrolidine ring in cis-4-amino-proline can induce both beta and gamma turn depending on the location of the intramolecular hydrogen bond. Turns have been identified as sites for posttranslational modification of proteins. This is particularly true with respect to phosphorylation and glycosylation. Additionally, formation of gamma-turns may initiate formation of beta-sheets in protein folding. Preparing analogues of naturally occurring hexapeptide echinocandin B bearing an aminoproline residue imparts greatly improved water solubility.
Fmoc-Pro(4-NH-Alloc) is used in peptide synthesis.
references
N-alpha-Benzoyl-Cis-4-Amino-L-Proline: A gamma-Turn Mimetic; Timothy P. Curran, Nicole M. Chandler, Robert J. Kennedy and Meghan T. Keaney; Tetrahedron Letters 1996; 37(12): 1933-1936.
Total Synthesis and Antifungal Evaluation of Cyclic Aminohexapeptides; Larry L. Klein, Leping Li, Hui-Ju Chen, Cynthia B. Curty, David A. DeGoey, David J. Grampovnik, Christina L. Leone, Sheela A. Thomas, Clinton M. Yeung, Kenneth W. Funk, Vimal Kishore, Edwin O. Lundell, Dariusz Wodka, Jon A. Meulbroek, Je€rey D. Alder, Angela M. Nilius, Paul A. Lartey and Jacob J. Plattner; Bioorganic & Medicinal Chemistry 2000; 8: 1677-1696.
The cis-4-Amino-L-proline Residue as a Scaffold for the Synthesis of Cyclic and Linear Endomorphin-2 Analogues;
Adriano Mollica, Francesco Pinnen, Azzurra Stefanucci, Federica Feliciani, Cristina Campestre, Luisa Mannina, Anatoly P. Sobolev, Gino Lucente, Peg Davis, Josephine Lai, Shou-Wu Ma, Frank Porreca, and Victor J. Hruby; J. Med. Chem. 2012; 55: 3027−3035. dx.doi.org/10.1021/jm201402v.
Tian, Yuan; Wang, Dongyuan; Li, Jingxu; Shi, Chuan; Zhao, Hui; Niu, Xiaogang; Li, Zigang Chemical Communications (2016), 52(59), 9275-9278. DOI:10.1039/C6CC04672J;
Roses, Cristina; Carbajo, Daniel; Sanclimens, Gloria; Farrera-Sinfreu, Josep; Blancafort, Adriana; Oliveras, Gloria; Cirac, Anna D.; Bardaji, Eduard; Puig, Teresa; Planas, Marta; et al Tetrahedron (2012), 68(23), 4406-4412. DOI:10.1016/j.tet.2012.02.003.
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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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