CAS 59587-94-9
:acide (4S)-4-[(tert-butoxycarbonyl)amino]-5-oxo-5-phénoxypentanoïque (nom non préféré)
Formule :C16H21NO6
InChI :InChI=1/C16H21NO6/c1-16(2,3)23-15(21)17-12(9-10-13(18)19)14(20)22-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,18,19)/t12-/m0/s1
Code InChI :UUGORLVQLJSWBX-LBPRGKRZSA-N
SMILES :CC(C)(C)OC(=O)N[C@@H](CCC(=O)O)C(=O)OC1=CC=CC=C1
Synonymes :- Boc-Glu-Phenyl Ester
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Boc-Glu-phenyl ester
CAS :Bachem ID: 4029196.
Formule :C16H21NO6Degré de pureté :> 99%Couleur et forme :White PowderMasse moléculaire :332.35(S)-4-((tert-Butoxycarbonyl)amino)-5-oxo-5-phenoxypentanoic acid
CAS :(S)-4-((tert-Butoxycarbonyl)amino)-5-oxo-5-phenoxypentanoic acidFormule :C16H21NO6Degré de pureté :97%Masse moléculaire :323.35(S)-4-((tert-Butoxycarbonyl)amino)-5-oxo-5-phenoxypentanoic acid
CAS :(S)-4-((tert-Butoxycarbonyl)amino)-5-oxo-5-phenoxypentanoic acidFormule :C16H21NO6Degré de pureté :97%Masse moléculaire :323.34Boc-Glu-phenyl ester
CAS :Boc-Glu-phenyl ester is an inhibitor of bacterial protein synthesis. It was first synthesized as a synthetic substrate for the enzyme staphylococcal protease and has been shown to be active against both human and staphylococcal cells, with activity against strains resistant to other antibiotics. Boc-Glu-phenyl ester inhibits the synthesis of proteins by binding to the catalytic site of the enzyme and preventing formation of peptide bonds. This inhibition leads to cell death due to a lack of critical proteins required for cellular function. Boc-Glu-phenyl ester is also specific for staphylococci, which may be due to its ability to inhibit the production of epidermolytic exotoxins.
Formule :C16H21NO6Degré de pureté :Min. 95%Masse moléculaire :323.34 g/mol





