Fmoc-Pro-OH [71989-31-6] HEADING_TITLE

N-Fmoc-L-proline

Other Names: Fmoc-L-Pro-OH

Catalog # AFP101 CAS 71989-31-6
Formula C20H19NO4 M.W. 337.4

Fmoc-Pro-OH

 

 

 

 

 

 

 

 

Fmoc-Pro-OH readily dissolves in DMF or NMP.  Proline is the only natural cyclic amino acid.  Proline residues disrupt β-sheet formation and strongly promote turn formation.  Proline residues in the first two positions of the C-terminal can promote diketopiperazine formation.  Using 2-chlorotrityl resin in place of Wang resin can prevent this undesired side reaction.

Products Similar to Fmoc-Pro-OH

Cat. # Product Cat. # Product
AFP191 Fmoc-Pro-OPfp ABP101 Boc-Pro-OH
AFP201 Fmoc-D-Pro-OH ABP201 Boc-D-Pro-OH
AFP291 Fmoc-D-Pro-OPfp ABP105 Boc-Pro-OMe
UFP102 Fmoc-beta-HPro-OH ABP220 Boc-D-Pro-OSu
UFP202 Fmoc-D-beta-HPro-OH UBP102 Boc-beta-HPro-OH
UFP131 Fmoc-azetidine-2-carboxylic acid UBP202 Boc-D-beta-HPro-OH
UFP231 Fmoc-D-azetidine-2-carboxylic acid UBP131 Boc-Azetidine-2-carboxylic acid
UFP101 Fmoc-Hyp-OH UBP231 Boc-D-Azetidine-2-carboxylic acid
UFP115 Fmoc-Hyp(tBu)-OH UBP101 Boc-Hyp-OH
UFP111 Fmoc-Hyp(Bzl)-OH UBP111 Boc-Hyp(Bzl)-OH
UFP106 Fmoc-Oic-OH UBP103 Boc-Hyp-OMe
UFC115 Fmoc-Thz-OH UBP104 Boc-Hyp-OEt
DFP101 Fmoc-Prolinol ABP110 Boc-4-Oxo-Pro-OH
AZP101 Z-Pro-OH ABP115 Boc-4-Oxo-Pro-OMe
AZP201 Z-D-Pro-OH UBC115 Boc-Thz-OH
AZP103 Z-Pro-NH2 UBC215 Boc-D-Thz-OH
DZP101 Z-Prolinol DBP201 Boc-D-Prolinol

MSDS