Phosphinate pseudopeptide are analogs of peptides containing phosphinate moiety in a place of the amide bond. Due to this, the organophosphorus fragment resembles the tetrahedral transition state of the amide bond hydrolysis. Additionally, it is also capable of coordinating metal ions, for example, zinc or magnesium ions. These two properties of phosphinate pseudopeptides make them an ideal candidate for metal-related protease inhibitors. This research investigates the influence of additional residue in the P2 position on the inhibitory properties of phosphinopeptides. The synthetic strategy is proposed, based on retrosynthetic analysis. The N-C-P bond formation in the desired compounds is conveniently available from the three-component con...
AbstractFragment-Based Identification of Phosphatase InhibitorsbyKatherine Anne RawlsDoctor of Philo...
The molecular structures of three phosphorus-based peptide inhibitors of aspartyl proteinases comple...
AbstractSome novel N-[1(RS)-carboxy-3-phenylpropyl]tripeptide p-aminobenzoates have been synthesised...
Several studies have demonstrated that the synthesis of phosphinic peptides is a very effective appr...
The nature of the interaction of the transition-state analogue inhibitor l-leucinephosphonic acid (L...
Metallocarboxypeptidases (MCPs) of the M14 family are Zn2+-dependent exoproteases present in almost ...
Petrosaspongiolide M (PM) is an anti-inflammatory marine metabolite that displays a potent inhibitor...
Serine proteases comprise about one-third of all proteases, and defective regulation of serine prote...
The oxytocinase subfamily of M1 aminopeptidases, consisting of ER aminopeptidase 1 (ERAP1), ER amino...
Funding: C.M.C. is funded by the Wellcome Trust (210486/Z/18/Z and [204821/Z/16/Z] to the University...
Seven crystal structures of alanyl aminopeptidase from <i>Neisseria meningitides</i> (the etiologica...
Phosphopantetheine is an essential biomolecule required for life. The enzyme phosphopantothenoylcyst...
Aminopeptidase N (APN; EC 3.4.11.2) purified from Escherichia coli has been crystallized with the op...
a-Amino-C-phosphinic acids and derivatives are an important group of compounds of synthetic and medi...
Intracellular leucine aminopeptidases (PepA) are metalloproteases from the family M17. These enzymes...
AbstractFragment-Based Identification of Phosphatase InhibitorsbyKatherine Anne RawlsDoctor of Philo...
The molecular structures of three phosphorus-based peptide inhibitors of aspartyl proteinases comple...
AbstractSome novel N-[1(RS)-carboxy-3-phenylpropyl]tripeptide p-aminobenzoates have been synthesised...
Several studies have demonstrated that the synthesis of phosphinic peptides is a very effective appr...
The nature of the interaction of the transition-state analogue inhibitor l-leucinephosphonic acid (L...
Metallocarboxypeptidases (MCPs) of the M14 family are Zn2+-dependent exoproteases present in almost ...
Petrosaspongiolide M (PM) is an anti-inflammatory marine metabolite that displays a potent inhibitor...
Serine proteases comprise about one-third of all proteases, and defective regulation of serine prote...
The oxytocinase subfamily of M1 aminopeptidases, consisting of ER aminopeptidase 1 (ERAP1), ER amino...
Funding: C.M.C. is funded by the Wellcome Trust (210486/Z/18/Z and [204821/Z/16/Z] to the University...
Seven crystal structures of alanyl aminopeptidase from <i>Neisseria meningitides</i> (the etiologica...
Phosphopantetheine is an essential biomolecule required for life. The enzyme phosphopantothenoylcyst...
Aminopeptidase N (APN; EC 3.4.11.2) purified from Escherichia coli has been crystallized with the op...
a-Amino-C-phosphinic acids and derivatives are an important group of compounds of synthetic and medi...
Intracellular leucine aminopeptidases (PepA) are metalloproteases from the family M17. These enzymes...
AbstractFragment-Based Identification of Phosphatase InhibitorsbyKatherine Anne RawlsDoctor of Philo...
The molecular structures of three phosphorus-based peptide inhibitors of aspartyl proteinases comple...
AbstractSome novel N-[1(RS)-carboxy-3-phenylpropyl]tripeptide p-aminobenzoates have been synthesised...