Chlormethine hydrochloride

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Cl(CH₂)₆OSi(CH₃)₃ CAS#: 34714-00-6 F.W.: 208.80

Analysis Note Assay (argentometric): &#8805 98.0 % Melting range (upper value): &#8804 73 &#176C Identity (IR): passes test

Analysis Note Assay (argentometric): &#8805 98.0 % Melting range (upper value): &#8804 73 &#176C Identity (IR): passes test

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.

Application Protein degrader builiding block C5 Lenalidomide-C 3 -NH 2 hydrochloride enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology . This conjugate contains a Cereblon

Application Protein degrader builiding block C5 Lenalidomide-C 6 -NH 2 hydrochloride enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology . This conjugate contains a Cereblon