Protease Inhibitors

BCN-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:Viscous liquidIC50&amp: Target:PEGs Alkyl/etherIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3

BCN-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:Viscous liquidIC50&amp: Target:PEGs Alkyl/etherIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3

HiTrap &#174 Benzamidine FF (high sub) is an excellent tool for removal of proteolytic activity from a protein. Application Benzamidine Sepharose &#8482 4 Fast FLow (high sub) is an excellent tool for removal and/or purification of trypsin and

Chemical structure: amino acid derivatives Biochem/physiol Actions A metalloprotease inhibitor selective for aminopeptidase. Bestatin is a competitive and specific inhibitor of leucine aminopeptidase, aminopeptidase B, and triamino peptidase.

Chemical structure: amino acid derivatives Biochem/physiol Actions A metalloprotease inhibitor selective for aminopeptidase. Bestatin is a competitive and specific inhibitor of leucine aminopeptidase, aminopeptidase B, and triamino peptidase.

Chemical structure: amino acid derivatives Biochem/physiol Actions A metalloprotease inhibitor selective for aminopeptidase. Bestatin is a competitive and specific inhibitor of leucine aminopeptidase, aminopeptidase B, and triamino peptidase.

Chemical structure: amino acid derivatives Biochem/physiol Actions A metalloprotease inhibitor selective for aminopeptidase. Bestatin is a competitive and specific inhibitor of leucine aminopeptidase, aminopeptidase B, and triamino peptidase.

Chemical structure: amino acid derivatives Biochem/physiol Actions A metalloprotease inhibitor selective for aminopeptidase. Bestatin is a competitive and specific inhibitor of leucine aminopeptidase, aminopeptidase B, and triamino peptidase.

Betulinic acid (BetA), a pentacyclic triterpene anticancer candidate, may be used to study its function and activity as an activator of mitochondrial pathway apoptosis involving p53- and CD95-independent mechanisms. Betulinic acid is used to study

Betulinic acid (BetA), a pentacyclic triterpene anticancer candidate, may be used to study its function and activity as an activator of mitochondrial pathway apoptosis involving p53- and CD95-independent mechanisms. Betulinic acid is used to study

Betulinic acid (BetA), a pentacyclic triterpene anticancer candidate, may be used to study its function and activity as an activator of mitochondrial pathway apoptosis involving p53- and CD95-independent mechanisms. Betulinic acid is used to study

Betulinic acid (BetA), a pentacyclic triterpene anticancer candidate, may be used to study its function and activity as an activator of mitochondrial pathway apoptosis involving p53- and CD95-independent mechanisms. Betulinic acid is used to study