117751-79-8

Upstream product

• 501-53-1 benzyl chloroformate 
• 75266-40-9 N-benzyloxycarbonyl-L-α-vinylglycine methyl ester 
• 75266-39-6 methyl (S)-2-<<(benzyloxy)carbonyl>amino>-4-(methylsulfinyl)butanoate 
• 83972-33-2 N-<(benzyloxy)carbonyl>-DL-methionine methyl ester 
• 4434-61-1 N-(benzyloxycarbonyl)methionine 
• 80656-34-4 N-<(benzoyloxy)carbonyl>-D,L-vinylglycine methyl ester 
• 56762-93-7 methyl (S)-2-(benzyloxycarbonylamino)-4-methylmercaptobutanoate 
• 1152-62-1 Cbz-Met-OH 

Downstream Products

• 142698-78-0 methyl (2S,3S)-2-<(benzyloxy)carbonylamino>-4-chloro-3-hydroxybutanoate 
• 129956-64-5 (S)-2-Benzyloxycarbonylamino-4-(4-chloro-phenylamino)-3-hydroxy-butyric acid methyl ester 
• 98777-31-2 (S)-2-Benzyloxycarbonylamino-3-hydroxy-4-phenylsulfanyl-butyric acid methyl ester 
• 98777-62-9 methyl DL-2-<(benzyloxy)carbonylamino>-4-chloro-3-hydroxybutanoate 
• 1219595-99-9 C₂₃H₂₈N₂O₈ 
• 1219595-87-5 C₂₃H₃₄N₂O₉ 
• 1219595-84-2 C₂₃H₂₈N₂O₇ 
• 1219595-98-8 C₂₃H₂₈N₂O₇ 
• 1219595-82-0 C₁₉H₂₈N₂O₇ 
• 129956-63-4 (Z)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-but-2-enoic acid methyl ester 
• 117751-72-1 methyl (2S,3R)-3-acetoxy-2-(benzyloxycarbonyl)aminobutanoate 
• 117751-88-9 O-acetyl-N-benzyloxycarbonyl-L-allothreonine methyl ester 
• 117751-71-0 2(S),3(R)-methyl 2-N-benzyloxycarbonylamino-4-bromo-3-hydroxybutanoate 
• 117751-87-8 (2S,3R)-2-Benzyloxycarbonylamino-4-bromo-3-hydroxy-butyric acid methyl ester 

Relevant academic research and scientific papers

INHIBITORS OF APOL1 AND METHODS OF USING SAME

The disclosure provides at least one entity chosen from compounds of formula (I), solid state forms of the same, compositions comprising the same, and methods of using the same, including use in treating focal segmental glomerulosclerosis (FSGS) and/or non-diabetic kidney disease (NDKD).

Structure and Stereochemistry of Three Phytotoxins, Syringomycin, Syringotoxin and Syringostatin, Produced by Pseudomonas syringae pv. syringae

The structures of two phytotoxins, syringomycin and syringotoxin, produced by Pseudomonas syringae pv. syringae, were determined.Several amino acid residues of syringomycin were different from those in the syringostatins.Syringotoxin B proved to be syringostatin A.The three kinds of phytotoxins showed close structural similarity, and the stereochemistry of their components was deduced and compared.

UNUSUAL α-AMINOACIDS FROM VINYLGLYCINE

The easily available L-vinylglycine derivative 1 is used in the synthesis of unusual multifunctional α-aminoacids such as 2 and 3.