29750-72-9

Upstream product

• 551-16-6 6-Aminopenicillanic Acid 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 35160-71-5 p-nitrobenzyl 6β-phthalimidylpenicillanate 
• 81658-72-2 p-nitrobenzyl 6β-aminopenicillanate p-toluenosulfonic acid salt 

Downstream Products

• 141044-39-5 Z(NO₂)-Ahx-penicillin-ONb 
• 112100-10-4 (2S,5R,6R)-1-aza-3,3'-dimethyl-6-(4-N-benzyloxycarbonylbutanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester 
• 129544-14-5 p-nitrobenzyl 6β-tritylaminopenicillanate 
• 726201-89-4 bis(p-nitrobenzyl) 6-[N-(p-nitrobenzyloxycarbonyl)glycyl-L-α-aminopimelyl]aminopenicillanate 
• 156662-97-4 p-nitrobenzyl 6β-tritylaminopenicillanate 1β-oxide 
• 156663-08-0 2-[(2R,3R)-2-(2,5-Dioxo-pyrrolidin-1-ylsulfanyl)-4-oxo-3-(trityl-amino)-azetidin-1-yl]-3-methyl-but-2-enoic acid 4-nitro-benzyl ester 
• 156663-02-4 p-nitrobenzyl (2R)-3-methyl-2-(4-oxo-5-tritylimino-3-thiazolidynyl)-3-butenoate 
• 156663-04-6 p-nitrobenzyl 3-methyl-2-(4-oxo-5-tritylimino-3-thiazolidynyl)-2-butenoate 
• 58244-55-6 4-nitrobenzyl(2S,5R,6R)-3,3-dimethyl-7-oxo-6-phenoxyacetamido-1-aza-4-thiabicyclo<3.2.0>heptane-2-carboxylate 
• 112078-60-1 (2S,5R,6R)-1-aza-3,3'-dimethyl-6-<(4R)-4-(benzyloxycarbonylamino)-5-(p-nitrobenzyloxycarbonyl)-butanamido>-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester 
• 112078-58-7 (2S,5R,6R)-1-aza-3,3'-dimethyl-6-(5-p-nitrobenzyloxycarbonylpentanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester 
• 112078-59-8 (2S,5R,6R)-1-aza-3,3'-dimethyl-6-(5-N-benzyloxycarbonylaminopentanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester 
• 87118-93-2 p-Nitrobenzyl 6-<3-(Carbamoyl)ureido>penicillanate 
• 87118-90-9 p-Nitrobenzyl 6-Thioureidopenicillanate 

Relevant academic research and scientific papers

The perfect penicillin? Inhibition of a bacterial DD-peptidase by peptidoglycan-mimetic β-lactams

6-(Glycyl-L-α-aminopimelyl)-aminopenicillanic acid and 7-(glycyl-L-α-aminopimelyl)-aminocephalosporanic acid have been synthesized as Streptomyces sp. peptidoglycan-mimetic β-lactams. These compounds inactivate the Streptomyces R61 DD-peptidase with rate