112592-90-2

Usage

Uses

Used in Pharmaceutical Industry:
(2S)-2-[[(2S)-1-[(2S)-6-amino-2-[[(2S,3R)-2-amino-3-hydroxy-butanoyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-5-(diaminomethylideneamino)pentanoic acid is used as a pharmaceutical agent for its potential therapeutic effects on various diseases and conditions. Its unique structure and functional groups allow it to interact with biological targets and modulate cellular processes, making it a promising candidate for drug development.
Used in Nutritional Supplements:
This peptide molecule can also be used in nutritional supplements to support overall health and well-being. Its role in physiological and biochemical functions may contribute to maintaining a balanced and healthy body.
Used in Cosmetic Industry:
(2S)-2-[[(2S)-1-[(2S)-6-amino-2-[[(2S,3R)-2-amino-3-hydroxy-butanoyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-5-(diaminomethylideneamino)pentanoic acid may be utilized in cosmetic products for its potential benefits to skin health and appearance. Its interaction with biological targets could lead to improved skin hydration, elasticity, and overall skin quality.

InChI:InChI=1/C21H40N8O6/c1-12(30)16(23)18(32)27-13(6-2-3-9-22)19(33)29-11-5-8-15(29)17(31)28-14(20(34)35)7-4-10-26-21(24)25/h12-16,30H,2-11,22-23H2,1H3,(H,27,32)(H,28,31)(H,34,35)(H4,24,25,26)/t12-,13+,14+,15+,16+/m1/s1

Upstream product

• 78432-02-7 Benzyloxycarbonylthreonyl(ε-tert-butoxycarbonyllysyl)prolylarginine 
• 154509-00-9 Boc-Thr(OBn)-Lys(2Cl,Z)-Pro-Arg(Tos)-OBn 
• 74-79-3 L-arginine 
• 3304-59-4 N-benzyloxycarbonyl-L-proline p-nitrophenyl ester 
• 55322-38-8 (α-Benzyloxycarbonyl-ε-tert-butoxycarbonyllysyl)prolylarginine 
• 60889-67-0 N-benzyloxycarbonyl-L-prolyl-L-arginine 
• 2212-69-3 N₂-benzyloxycarbonyl-N₆-t-butoxycarbonyl-L-lysine 4-nitrophenyl ester 
• 154508-97-1 Boc-Lys(2Cl,Z)-Pro-Arg(Tos)-OBn 
• 66336-81-0 Boc-Pro-Arg(Tos)-OBn 
• 66336-82-1 H-Pro-Arg(Tos)-OBn 
• 61543-20-2 Boc-Arg(Tos)-OBzl 
• 13836-37-8 Boc-Arg(Tos)-OH 
• 29388-63-4 H-Arg(Tos)-OBzl 

Relevant academic research and scientific papers

Enantiospecific C-H Activation Using Ruthenium Nanocatalysts

The activation of C-H bonds has revolutionized modern synthetic chemistry. However, no general strategy for enantiospecific C-H activation has been developed to date. We herein report an enantiospecific C-H activation reaction followed by deuterium incorporation at stereogenic centers. Mechanistic studies suggest that the selectivity for the α-position of the directing heteroatom results from a four-membered dimetallacycle as the key intermediate. This work paves the way to novel molecular chemistry on nanoparticles.

Thioacylating Agents. Use of Thiobenzimidazolone Derivatives for the Preparation of Thiotuftsin Analogs.

The properties and characteristic reactions of thioacylating reagents 1 are described.These reagents are able to introduce thioamide linkages into a growing peptide at a specific site in the sequence.The generality and efficiency of this methodology is demonstrated by the synthesis of the three monothioanalogues of tuftsin.

Method for protecting guanidino group and restoring the same

A guanidino group in an amino acid or a peptide can be protected with a specific protective group, i.e. lower alkoxybenzenesulfonyl group or tri-lower alkylbenzenesulfonyl group, and the protective group may easily be removed without affecting the amino acid or the peptide to be derived from the protected amino acid or peptide. Thus, the method is useful in the related chemical industries, especially in the peptide synthesis.