1316672-53-3Relevant academic research and scientific papers
Synthesis and biological activity of N-substitutedtetrahydro-γ- Carbolines containing peptide residues
Sokolova, Nadezhda V.,Nenajdenko, Valentine G.,Sokolov, Vladimir B.,Vinogradova, Daria V.,Shevtsova, Elena F.,Dubova, Ludmila G.,Bachurin, Sergey O.
, p. 155 - 162 (2014/02/14)
The synthesis of novel peptide conjugates of N-substituted-tetrahydro- γ-carbolines has been performed using the sequence of the Ugi multicomponent reaction and Cu(I)-catalyzed click chemistry. The effect of obtained γ-carboline-peptide conjugates on the
Design and synthesis of bile acid-peptide conjugates linked via triazole moiety
Sokolova, Nadezhda V.,Latyshev, Gennadij V.,Lukashev, Nikolay V.,Nenajdenko, Valentine G.
supporting information; experimental part, p. 4921 - 4926 (2011/08/22)
A conjugation of bile acids with peptides via Cu(i)-catalyzed click chemistry has been described. Novel bile acid-peptide conjugates linked via a 1,2,3-triazole moiety based on cholic, deoxycholic and lithocholic acid derivatives were synthesized using Cu
Synthesis and testing of trifluoromethyl-containing phosphonate-peptide conjugates as inhibitors of serine hydrolases
Sokolova, Nadezhda V.,Nenajdenko, Valentine G.,Sokolov, Vladimir B.,Serebryakova, Olga G.,Makhaeva, Galina F.
supporting information; experimental part, p. 7216 - 7218 (2012/01/15)
A modification of novel fluorinated organophosphorous compounds containing terminal alkyne group by different azidopeptides via Cu(I)-catalyzed click chemistry has been described. The inhibitor activity of trifluoromethyl- containing methylphosphonates an
