104199-72-6

Upstream product

• 34619-03-9 tert-butyldicarbonate 
• 104199-71-5 N¹,N⁸-bis(benzyloxycarbonylglycyl)-spermidine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 73453-98-2 1-(4-aminobutyl)-1,2,3,4,5,6-hexahydropyrimidine 
• 104199-70-4 (2-{3-[4-(2-Benzyloxycarbonylamino-acetylamino)-butyl]-tetrahydro-pyrimidin-1-yl}-2-oxo-ethyl)-carbamic acid benzyl ester 
• 2899-60-7 Cbz-Gly-ONSuc 
• 124-20-9 N-(3-aminopropyl)-1,4-diaminobutane 
• 60341-62-0 carbobenzyloxyglycinesuccinimido ester 

Downstream Products

• 941297-01-4 C₄₂H₅₉N₇O₁₀ 
• 941297-04-7 C₄₀H₅₅N₇O₁₀ 
• 1026698-09-8 C₄₀H₅₇N₇O₁₀ 
• 96304-42-6 trypanothione disulfide 

Relevant academic research and scientific papers

The synthesis and inhibitory activity of dethiotrypanothione and analogues against trypanothione reductase

(Chemical Equation Presented) Trypanothione reductase (TR) catalyzes the NADPH-dependent reduction of trypanothione disulfide (1). TR plays a central role in the trypanosomatid parasite's defense against oxidative stress and has emerged as a promising tar

Synthesis and NMR Characterization of the Trypanosomatid Metabolite, N1,N8-Bis(glutathionyl)spermidine Disulphide (Trypanothione Disulphide)

An optimized chemical synthesis of the novel trypanosomatid metabolite, N1,N8-bis(glutathionyl)spermidine (trypanothione disulphide) is described, and its solution structure has been investigated by NMR spectroscopy.The 1H, 13C, and