Bio-Connect
Chemical Structure
Chemical Structure
Chemical Structure

Tubastatin A [1239262-52-2]

Research Use Only
AG-CR1-3900
AdipoGen Life Sciences
CAS Number1239262-52-2
Product group Chemicals
Estimated Purity>98%
Molecular Weight335.4
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Tubastatin A
  • Delivery Days Customer
    10
  • CAS Number
    1239262-52-2
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Molecular Formula
    C20H21N3O2
  • Molecular Weight
    335.4
  • Scientific Description
    Cell permeable potent and selective class IIb histone deacetylase 6 (HDAC6) inhibitor (IC50=15nM, >1000-fold selective against other HDACs and 60-fold for HDAC8). Neuroprotective. Effectively prevents neuronal cell death (by >95% at 10microM) upon oxidative stress induction by HCA and selectively induces cellular alpha-tubulin, but not histone H4, hyperacetylation (2.5 to 5microM) in primary rat cortical neuron cultures. Improves cognition in Alzheimers disease transgenic mice. Exhibits cardioprotective and anticancer chemotherapeutic activities. Reduces tumor growth and cell proliferation and induces cell cycle arrest in G1. Inhibits TNFalpha (IC50=272nM) and IL-6 (IC50=712nM) in LPS-stimulated human THP-1 macrophages and displays anti-inflammatory activity in animal models. Antileishmanial. HDAC6 deacetylates tubulin, HSP90 and the core histones (H2A, H2B, H3, H4). Histone deacetylases act via the formation of large multiprotein complexes. HDAC6 plays an important role in microtubule-dependent cell motility, transcriptional regulation, degradation of misfolded proteins and cell cycle and is involved in autophagy, inflammation, cancer and neurodegeneration. - Chemical. CAS: 1252003-15-8. Formula: C20H21N3O2. MW: 335.4. Cell permeable potent and selective class IIb histone deacetylase 6 (HDAC6) inhibitor (IC50=15nM, >1000-fold selective against other HDACs and 60-fold for HDAC8). Neuroprotective. Effectively prevents neuronal cell death (by >95% at 10microM) upon oxidative stress induction by HCA and selectively induces cellular alpha-tubulin, but not histone H4, hyperacetylation (2.5 to 5microM) in primary rat cortical neuron cultures. Improves cognition in Alzheimers disease transgenic mice. Exhibits cardioprotective and anticancer chemotherapeutic activities. Reduces tumor growth and cell proliferation and induces cell cycle arrest in G1. Inhibits TNFalpha (IC50=272nM) and IL-6 (IC50=712nM) in LPS-stimulated human THP-1 macrophages and displays anti-inflammatory activity in animal models. Antileishmanial. HDAC6 deacetylates tubulin, HSP90 and the core histones (H2A, H2B, H3, H4). Histone deacetylases act via the formation of large multiprotein complexes. HDAC6 plays an important role in microtubule-dependent cell motility, transcriptional regulation, degradation of misfolded proteins and cell cycle and is involved in autophagy, inflammation, cancer and neurodegeneration.
  • SMILES
    CN1CCC2=C(C1)C1=CC=CC=C1N2CC1=CC=C(C=C1)C(=O)NO
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200