Fmoc-L-Pro(4-CF3)-OH (2S,4S)

Chemical name: (2S,4S)-1-(9-Fluorenylmethyloxycarbonyl)-4-trifluoromethyl-pyrrolidine-2-carboxylic acid // Synonyms: (2S,4S)-Fmoc-4-trifluoromethyl-pyrrolidine-2-carboxylic acid, Fmoc-4-trifluoromethyl-proline (2S,4S), Fmoc-Pro(4-CF3)-OH (2S,4S)

  • Product code:FAA4320
  • CAS No.:1242934-32-2
  • Formula:C21H18F3NO4
  • Storage temperature:2-8°C
  • Molecular weight:405.37 g/mol

from €225.00

Grouped product items
Qty Packing unit Price SKU Availability
250 mg
€225.00
FAA4320.0250
<10 business days
1 g
€650.00
FAA4320.0001
<10 business days
5 g
€2,600.00
FAA4320.0005
<10 business days
references

The Outcomes of Decorated Prolines in the Discovery of Antimicrobial Peptides from Temporin-L; E. Buommino, A. Carotenuto, I. Antignano, R. Bellavita, B. Casciaro, M. R. Loffredo, F. Merlino, E. Novellino, M. L. Mangoni, F. P. Nocera, D. Brancaccio, P. Punzi, D. Roversi, R. Ingenito, E. Bianchi and P. Grieco; ChemMedChem 2019; 14: 1283-1290. DOI: https://doi.org/10.1002/cmdc.201900221.

Comparative effects of trifluoromethyl- and methyl-group substitutions in proline; V. Kubyshkin, S. Pridma and N. Budisa; New Journal of Chemistry 2018; 42: 13461-13470. DOI: https://doi.org/10.1039/c8nj02631a.

Discovery of Pyrrolidine-Containing GPR40 Agonists: Stereochemistry Effects a Change in Binding Mode; E. A. Jurica, X. Wu, K. N. Williams, A. S. Hernandez, D. S. Nirschl, R. A. Rampulla, A. Mathur, M. Zhou, G. Cao, C. Xie, B. Jacob, H. Cai, T. Wang, B. J. Murphy, H. Liu, C. Xu, L. K. Kunselman, M. B. Hicks, Q. Sun, D. M. Schnur, D. F. Sitkoff, E. A. Dierks, A. Apedo, D. B. Moore, K. A. Foster, M. E. Cvijic, R. Panemangalore, N. A. Flynn, B. D. Maxwell, Y. Hong, Y. Tian, J. J. Wilkes, B. A. Zinker, J. M. Whaley, J. C. Barrish, J. A. Robl, W. R. Ewing and B. A. Ellsworth; Journal of medicinal chemistry 2017; 60: 1417-1431. DOI: https://doi.org/10.1021/acs.jmedchem.6b01559.

gamma-(S)-Trifluoromethyl proline: evaluation as a structural substitute of proline for solid state (19)F-NMR peptide studies; V. Kubyshkin, S. Afonin, S. Kara, N. Budisa, P. K. Mykhailiuk and A. S. Ulrich; Org Biomol Chem 2015; 13: 3171-3181. DOI: https://doi.org/10.1039/c5ob00034c.


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