(R)-Zelebrudomide is a Bruton’s Tyrosine Kinase (BTK) degrader synthesized as an isomer of the PROTAC compound Zelebrudomide. It selectively induces the degradation of BTK, a crucial target in the treatment of various hematological malignancies. This compound is utilized in research to investigate its potential therapeutic applications in autoimmune diseases and cancers where BTK is implicated.
(R)-Zelebrudomide is a Bruton’s Tyrosine Kinase (BTK) degrader synthesized as an isomer of the PROTAC compound Zelebrudomide. It selectively induces the degradation of BTK, a crucial target in the treatment of various hematological malignancies. This compound is utilized in research to investigate its potential therapeutic applications in autoimmune diseases and cancers where BTK is implicated.
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