35010-96-9

Usage

Chemical Properties

White powder

Upstream product

• 61058-42-2 Z-Pro-Gly-OMe 
• 1668-10-6 glycinamide hydrochloride 
• 1148-11-4 N-Benzyloxycarbonyl-L-proline 
• 3304-59-4 N-benzyloxycarbonyl-L-proline p-nitrophenyl ester 

Downstream Products

• 136315-46-3 N^α-Benzyloxycarbonyl-L-leucyl-L-arginyl-L-prolylglycine amide acetate sesquihydrate 
• 61058-42-2 Z-Pro-Gly-OMe 
• 2766-18-9 N-carbobenzoxyprolylglycine 
• 97985-95-0 {(S)-1-[(S)-1-{[((S)-1-{(S)-1-[(S)-2-(Carbamoylmethyl-carbamoyl)-pyrrolidine-1-carbonyl]-4-guanidino-butylcarbamoyl}-3-methyl-butylcarbamoyl)-methyl]-carbamoyl}-2-(4-hydroxy-phenyl)-ethylcarbamoyl]-2-hydroxy-ethyl}-carbamic acid benzyl ester 
• 97985-97-2 amide of benzyloxycarbonylarginylprolylglycine 
• 51776-33-1 luteinizing hormone-releasing hormone (4-10) 
• 132478-01-4 (S)-1-[(S)-2-((S)-2-{(R)-2-[(S)-2-((S)-2-Amino-3-hydroxy-propionylamino)-3-(4-hydroxy-phenyl)-propionylamino]-3-phenyl-propionylamino}-4-methyl-pentanoylamino)-5-guanidino-pentanoyl]-pyrrolidine-2-carboxylic acid carbamoylmethyl-amide 
• 77659-17-7 Z-Pro-Ser-Tyr-D-Ala-Leu-(O₂N)Arg-Pro-Gly-NH₂ 
• 77659-12-2 Z-D-Ala-Leu-(O₂N)Arg-Pro-Gly-NH₂ 
• 41271-84-5 Z-Leu-(O₂N)Arg-Pro-Gly-NH₂ 
• 41271-83-4 Z-(O₂N)Arg-Pro-Gly-NH₂ 

Relevant academic research and scientific papers

PEPTIDE DEFORMYLASE INHIBITORS

Novel PDF inhibitors of Formula (I), pharmaceutical compositions thereof and their use in treating bacterial infections are described.

Synthesis and biological evaluation of analogues of the antibiotic pantocin B

Strains of the bacteria Erwinia herbicola produce antibiotics that effectively control E. amylovora, the bacterial pathogen responsible for the plant disease fire blight. Pantocin B was the first of these antibiotics to be characterized, and a flexible sy

Large-Scale Synthesis of Mammalian Gonadoliberin without Protection of Side-Chain Functions

A simple, large-scale preparation of mammalian gonadoliberin was elaborated using classical solution methods without protecting side-chain functions.At the final stage, a hexapeptide segment was condensed with the corresponding tetrapeptide and the obtain

SYNTHESIS OF 3(NH2); Pro3; D-Ala6>- and 2(NO2); Pro3; D-Ala6>LULIBERINS

In order to study the influence of substituents of the aromatic ring of D-phenylalanine on the inhibiting capacity of luliberian analogs, we have synthesized two new analogs: 2; Pro3; D-Ala6>- and