76338-91-5

Upstream product

• 67-56-1 methanol 
• 76338-90-4 α-amino-γ-bromobutyric acid hydrobromide 
• 82636-35-9 methyl α-amino-γ-bromobutyrate hydrochloride 
• 501-53-1 benzyl chloroformate 
• 1885-14-9 phenyl chloroformate 

Downstream Products

• 126116-63-0 N-benzyloxycarbonyl-O-<(6'-hydroxy-4,4'-dimethoxydihydrochalcone)-2'-yl>homoserine methyl ester 
• 81546-76-1 2-Amino-4-(3-benzyloxycarbonylamino-3-methoxycarbonyl-propylsulfanyl)-butyric acid 
• 84677-06-5 (benzyloxycarbonylamino)cyclopropanecarboxylic acid 
• 84677-05-4 methyl 1-(((benzyloxy)carbonyl)amino)cyclopropane-1-carboxylate 
• 81546-71-6 methyl N^α-benzyloxycarbonylamino-γ-nitrobutyrate 
• 93000-22-7 19-O-<3-<(benzyloxycarbonyl)amino>-3-carbomethoxypropyl>steviolbioside 
• 245368-86-9 2-amino-4-nitro-butyric acid methyl ester 
• 245368-88-1 2-[N-[4-[N-[(2-acetamido-4(3H)oxopyrido[2,3-d]pyrimidin-6-yl)methyl]formamido]benzoyl]amino]-4-nitrobutanoic acid methyl ester 
• 245368-87-0 2-{4-[(2-acetylamino-4-oxo-3,4,5,6,7,8-hexahydro-pyrido[2,3-d]pyrimidin-6-ylmethyl)-formyl-amino]-benzoylamino}-4-nitro-butyric acid methyl ester 
• 126116-64-1 N-benzyloxycarbonyl-O-<(6'-hydroxy-4,4'-dimethoxydihydrochalcone)-2'-yl>homoserine 
• 126116-69-6 homoseryl>glycine 
• 126116-68-5 N-benzyloxycarbonyl-homoseryl>glycine ethyl ester 
• 126116-66-3 homoseryl>glycine benzyl ester 
• 81546-73-8 dicyclohexylammonium N^α-benzyloxycarbonylamino-γ-nitrobutyrate 

Relevant academic research and scientific papers

DIAZEPINONE DERIVATIVES AND THEIR USE IN THE TREATMENT OF HEPATITIS B INFECTIONS

Provided herein are compounds of formula (I) and (V) useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.

Synthesis of the γ-sulfinic acid and γ-nitro analogues of 5- deazatetrahydrofolic acid

Analogues of 5-deaza-5,6,7,8-tetrahydrofolic acid with a γ-sulfinic acid group or γ-nitro group in place of the γ-carboxyl group of the glutamate side chain were synthesized as diastereomeric mixtures, and were tested for their ability to inhibit the grow

Design and synthesis of phosphonate inhibitors of glutamine synthetase

Inhibitors 1-4 have been shown previously to undergo enzymatic phosphorylation by glutamine synthetase (GS). Phosphonates 6-9 were designed as chemically stable analogues of these phosphorylated inhibitors, incorporating either a tetrahedral sulfur group

Comestibles sweetened with alpha amino acid dihydrochalcones

Dihydrochalcones of the formula STR1 are disclosed wherein X is H or OH and R is a lower alkyl. These materials are useful as sweeteners for edibles. A process for preparing these compounds using a novel intermediate is disclosed as are acid and base neutralization products of the subject dihydrochalcones.

Flavonone precursors for alpha amino acid dihydrochalcones

Dihydrochalcones of the formula STR1 are disclosed wherein X is H or OH and R is a lower alkyl. These materials are useful as sweeteners for edibles. A process for preparing these compounds using a novel intermediate is disclosed as are acid and base neutralization products of the subject dihydrochalcones.

Alpha amino acid dihydrochalcones

Dihydrochalcones of the formula STR1 are disclosed wherein X is H or OH and R is lower alkyl. These materials are useful as sweeteners for edibles. A process for preparing these compounds using a novel intermediate is disclosed as are acid and base neutralization products of the subject dihydrochalcones.