59524-62-8

Upstream product

• 18814-49-8 tert-butoxycarbonyl-L-alanyl-D-isoglutamine benzyl ester 
• 18800-75-4 D-γ-methyl isoglutamine hydrochloride 
• 18814-49-8 Boc-L-alanyl-D-isoglutamine benzyl ester 

Downstream Products

• 123725-39-3 N-<(2RS,2'S)-2-<2-(benzyloxymethyl)-2-(tert-butoxycarbonylamino)ethoxy>propanoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 142489-58-5 N-(7-oxotetradecanoyl)-L-alanyl-D-isoglutamine benzyl ester 
• 141949-72-6 (R)-4-{(S)-2-[2-(2-tert-Butoxycarbonylamino-cyclohexyloxy)-acetylamino]-propionylamino}-4-carbamoyl-butyric acid benzyl ester 
• 56772-92-0 muramyl dipeptide 
• 87137-44-8 C₄₂H₄₂N₈O₁₇^(2-)*2Na⁽¹⁺⁾ 
• 123418-20-2 N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester 
• 123418-18-8 N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester 
• 62853-36-5 L-alanyl-(γ-benzyl ester D-isoglutamine) 
• 85472-21-5 6-(benzyloxycarbonylamino)hexyl β-glycoside of N-acetyl-4,6-O-benzylidenemuramyl-L-alanyl-D-isoglutamine benzyl ester 
• 137040-49-4 (2S,4R,5R,6R)-6-((R)-1,2-Dihydroxy-ethyl)-4,5-dihydroxy-tetrahydro-pyran-2-carboxylic acid [(S)-1-((R)-3-benzyloxycarbonyl-1-carbamoyl-propylcarbamoyl)-ethylcarbamoyl]-methyl ester 
• 137040-52-9 (R)-4-Carbamoyl-4-((S)-2-{[(2S,4R,5R,6R)-6-((R)-1,2-dihydroxy-ethyl)-4,5-dihydroxy-tetrahydro-pyran-2-carbonyl]-amino}-propionylamino)-butyric acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of cyclopropanoid 2-epi-muramyldipeptide analogues as potential immunostimulants

The preparation of cyclopropanoid 2-epi-muramyldipeptide analogues from suitable substituted cyclopropylamines is described.

Synthesis of cyclopropanoid analogues of N-acyl-muramyldipeptide as potential immunostimulants

The preparation of diastereomerically pure cyclopropanoid muramyldipeptide analogues from suitable substituted cyclopropylamines is described.

Synthesis of Spacered Cyclopropanoid Muramyldipeptide Analogues as Potential Immunostimulants

A novel class of cyclopropanoic muramyldipeptide analogues containing an additional methylene spacer between the cyclopropane ring and the lactyl residue has been prepared by a straightforward synthesis starting from isopropyl (R)-lactate.

Synthesis of Acyclic Analogs of N-Acetylmuramyl-L-alanyl-D-isoglutamine (MDP)

The synthesis of the acyclic MDP analogs 27-37 is described, the carbohydrate moiety of muramic acid being replaced by acyclic amino alcohol structures.Their preparation was accomplished by hydrolytic cleavage of the cyclic, disubstituted 3-morpholinones

Novel immunological adjuvant compounds and methods of preparation thereof

This application relates to novel immunological adjuvant compounds of the formula: STR1 wherein each of R and R1 are the same or different and are hydrogen or an acyl radical; R2 is an unsubstituted or substituted alkyl radical, or an unsubstituted or substituted aryl radical; X is an aminoacyl moiety; and Y is D-isoasparagine or D-isoglutamine.