19870-47-4

Upstream product

• 113-98-4 Penicillin G potassium 
• 541-41-3 chloroformic acid ethyl ester 
• 39879-63-5 penicillin-G N-ethylpiperidine salt 

Downstream Products

• 62984-93-4 4-[6β-(2-phenyl-acetylamino)-penicillanoyl]-morpholine 
• 122214-49-7 6β-(2-phenyl-acetylamino)-penicillanic acid-(2-morpholino-ethyl ester) 
• 119621-35-1 6β-(2-phenyl-acetylamino)-penicillanic acid-(3-diethylamino-propyl ester) 
• 122218-31-9 ethyl-bis-{2-[6β-(2-phenyl-acetylamino)-penicillanoyloxy]-ethyl}-amine 
• 809-71-2 6β-(2-phenyl-acetylamino)-penicillanic acid 4-dimethylamino-phenyl ester 
• 69578-02-5 S-phenyl benzylpenicillinthiocarboxylate 
• 80127-23-7 allyl (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 
• 23536-57-4 N-[6β-(2-phenyl-acetylamino)-penicillanoyl]-glycine 
• 3689-73-4 penethacillin 
• 101634-63-3 benzylpenicillin-phenyl ester 
• 1947-61-1 <2S-<2α,5α,6β>>-7-oxo-6-<(phenylacetyl)amino>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxamide 
• 76002-95-4 <2H3>-methyl benzylpenicillinate 
• 23536-54-1 (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid ethylamide 
• 142762-72-9 <2S-<2α,5α,6β>>-N,N'-<1,2-ethanediyl>bis<3,3-dimethyl-7-oxo-6-<(phenylacetyl)amino>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxamide> 

Relevant academic research and scientific papers

A series of penicillin derived C2-symmetric inhibitors of HIV-1 proteinase: synthesis, mode of interaction, and structure-activity relationships.

The C2-symmetric diester 1 was identified by random screening as a novel inhibitor of HIV-1 proteinase. This led to the preparation of a series of related more potent amides from readily accessible penicillins. Many of the compounds showed potent antivira

Studies related to Penicillins. Part 20. The Mechanism of the Rearangement of Methyl Benzylpenicillinate to Methyl Benzylpenillonate

In boiling benzene containing a trace of iodine, methyl benzylpenicillinate (1) isomerises to methyl benzylpenillonate (10a).The rearrangement is triggered by a 4,7-bond cleavage of the penicillinate (1a) and probably involves the formation of methyl (4S)