Fmoc-L-Pro(4-guanidino-Pbf)-OH (2S,4R)

Chemical name: (2S,4R)-1-(9-Fluorenylmethyloxycarbonyl)-4-(3-(2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran-5-ylsulfonyl)guanidino)pyrrolidine-2-carboxylic acid // Synonyms: (2S,4R)-Fmoc-4-(N'-Pbf-guanidino)-pyrrolidine-2-carboxylic acid,(2S,4R)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)-4-(3-(2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran-5-ylsulfonyl)guanidino)pyrrolidine-2- carboxylic acid, Fmoc-Pro(4-guanidino-Pbf)-OH(2S,4

  • Product code:FAA5220
  • CAS No.:1864002-98-1
  • Formula:C34H38N4O7S
  • Storage temperature:2-8°C
  • Molecular weight:646.75 g/mol

from €300.00

Grouped product items
Qty Packing unit Price SKU Availability
250 mg
€300.00
FAA5220.0250
<10 business days
1 g
€900.00
FAA5220.0001
<10 business days
5 g
€3,600.00
FAA5220.0005
>20 business days
Safety Data Sheets
references

Structural Development of Cell-Penetrating Peptides Containing Cationic Proline Derivatives; H. Kobayashi, T. Misawa, M. Oba, N. Hirata, Y. Kanda, M. Tanaka, K. Matsuno, Y. Demizu; Chem. Pharm. Bulletin 2018; 66(5): 575-580. https://doi.org/10.1248/cpb.c18-00079.

Effect of Preorganized Charge-Display on the Cell-Penetrating Properties of Cationic Peptides; Y. A. Nagel, P. S. Raschle, H. Wennemers; Angew. Chem. Int. Ed. 2017; 56(1): 122-126. https://doi.org/10.1002/anie.201607649.

Plasmid DNA delivery by arginine-rich cell-penetrating peptides containing unnatural amino acids; T. Kato, H. Yamashita, T. Misawa, K. Nishida, M. Kurihara, M. Tanaka, Y. Demizu, M. Oba; Bioorg. Med. Chem. 2016; 24(12): 2681-2687. https://doi.org/10.1016/j.bmc.2016.04.031.

Substitution of Arginine with Proline and Proline Derivatives in Melanocyte-Stimulating Hormones Leads to Selectivity for Human Melanocortin 4 Receptor; H. Qu, M. Cai, A. V. Mayorov, P. Grieco, M. Zingsheim, D. Trivedi, V. J. Hruby; J. Med. Chem. 2009; 52(12): 3627-3635. https://doi.org/10.1021/jm801300c.

Rational Design of a-Conotoxin Analogues Targeting a7 Nicotinic Acetylcholine Receptors; C. Armishaw, A. A. Jensen, T. Balle, R. J. Clark, K. Harpsøe, C. Skonberg, T. Liljefors, K. Strømgaard; J. Biol. Chem. 2009; 284(14): 9498-9512. https://doi.org/10.1074/jbc.M806136200.

Synthesis of Proteins Containing Modified Arginine Residues; A. K. Choudhury, S. Y. Golovine, L. M. Dedkova, S. M. Hecht; Biochem. 2007; 46(13): 406-4076. https://doi.org/10.1021/bi062042r.

Practical and Efficient Synthesis of Orthogonally Protected Constrained 4-Guanidinoprolines; M. Tamaki, G. Han, V. J. Hruby; J. Org. Chem. 2001; 66(3): 1038-1042. https://doi.org/10.1021/jo005626m.

Synthesis of Alanine and Proline Amino Acids with Amino or Guanidinium Substitution on the Side Chain; Z. Zhang, A. V. Aerschot, C. Hendrix, R. Busson, F. David, P. Sandra, P. Herdewijn; Tetrahedron 2000; 56(16): 2513-2522. https://doi.org/10.1016/S0040-4020(00)00123-X.

Conformationally restricted arginine analogs; T. R. Webb, C. Eigenbrot; J. Org. Chem. 1991; 56(9): 3009-3016. https://doi.org/10.1021/jo00009a016.


* Disclaimer
Prices are excl. tax, excl. shipping.
We refer to our general terms and conditions.
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.

Do you need further information about this product?

get in contact

Quick contact

Please send me more information about

Posts

We found other products you might like!