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MS6105

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Catalog No. T81747Cas No. 2891709-58-1

MS6105 is a chimeric LDH protein hydrolysis-targeted PROTAC that degrades LDHA and LDHB efficiently, with its activity contingent on both time and the ubiquitin-proteasome system, exhibiting anticancer properties [1]. Additionally, as a click chemistry reagent possessing an Alkyne group, MS6105 can partake in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with Azide-bearing molecules.

MS6105

MS6105

😃Good
Catalog No. T81747Cas No. 2891709-58-1
MS6105 is a chimeric LDH protein hydrolysis-targeted PROTAC that degrades LDHA and LDHB efficiently, with its activity contingent on both time and the ubiquitin-proteasome system, exhibiting anticancer properties [1]. Additionally, as a click chemistry reagent possessing an Alkyne group, MS6105 can partake in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with Azide-bearing molecules.
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Product Introduction

Bioactivity
Description
MS6105 is a chimeric LDH protein hydrolysis-targeted PROTAC that degrades LDHA and LDHB efficiently, with its activity contingent on both time and the ubiquitin-proteasome system, exhibiting anticancer properties [1]. Additionally, as a click chemistry reagent possessing an Alkyne group, MS6105 can partake in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with Azide-bearing molecules.
In vitro
MS6105 (compound 22), when administered at concentrations ranging from 10 nM to 10 μM over 48 hours, effectively induces time- and concentration-dependent degradation of LDHA and LDHB in PANC1 cells, exhibiting DC50 values of 38 nM for LDHA and 74 nM for LDHB, respectively [1].
Chemical Properties
Molecular Weight1228.59
FormulaC65H81N9O9S3
Cas No.2891709-58-1
Storage & Solubility Information
StorageShipping with blue ice.

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