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Chemical Structure
Chemical Structure
Chemical Structure

PTACH [848354-66-5]

Research Use Only
CDX-P0063
Chemodex
CAS Number848354-66-5
Product group Chemicals
Estimated Purity>95%
Molecular Weight390.56
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    PTACH [848354-66-5]
  • Delivery Days Customer
    10
  • CAS Number
    848354-66-5
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Hazard Information
    Danger
  • Molecular Formula
    C20H26N2O2S2
  • Molecular Weight
    390.56
  • Scientific Description
    Chemical. CAS: 848354-66-5. Formula: C20H26N2O2S2. MW: 390.56. Synthetic. Non-hydroxamate HDAC inhibitor (HDACi) (IC50: 32, 48 and 41nM for HDAC4, HDAC1 and HDAC6, respectively). Cell-permeable prodrug that is intracellularly converted to a potent HDAC inhibitor. Predicted to exhibit a similar HDAC binding mode as that of SAHA, interacting with the active-site zinc targeting group. Shown to exhibit comparable antiproliferative and apoptotic activity as SAHA against various cancer cell lines. Inhibits growth of various cancer cells in vitro (EC50 = 1.1 - 9.1mM). Also reactivates latent HIV-1 gene expression. - Non-hydroxamate HDAC inhibitor (HDACi) (IC50: 32, 48 and 41nM for HDAC4, HDAC1 and HDAC6, respectively). Cell-permeable prodrug that is intracellularly converted to a potent HDAC inhibitor. Predicted to exhibit a similar HDAC binding mode as that of SAHA, interacting with the active-site zinc targeting group. Shown to exhibit comparable antiproliferative and apoptotic activity as SAHA against various cancer cell lines. Inhibits growth of various cancer cells in vitro (EC50 = 1.1 - 9.1microM). Also reactivates latent HIV-1 gene expression.
  • SMILES
    CC(C)C(=O)SCCCCCCC(=O)NC1=NC(=CS1)C1=CC=CC=C1
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352200