TTA-A2

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Based on 1 publication(s) in Google Scholar

TTA-A2 is a potent, selective and orally active t-type voltage gated calcium channel antagonist with reduced pregnane X receptor (PXR) activation. TTA-A2 is equally potent against the Cav3.1 (a1G) and Cav3.2 (a1H) channels with IC50 values of 89 nM and 92 nM, respectively, at -80 and -100 mV holding potentials. TTA-A2 can be used for the research of a variety of human neurological diseases, including sleep disorders and epilepsy.

For research use only. We do not sell to patients.

  • Purity: 99.33%
  • CAS No.: 953778-63-7
  • Formula: C20H21F3N2O2
  • Molecular Weight:378.39
  • Storage:
    Powder   -20°C, 3 years ; In solvent   -80°C, 6 months , -20°C, 1 month
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