NNC 55-0396

NNC 55-0396

CAT N°: 17216
Price:

From 75.00 63.75

NNC 55-0396 is a selective inhibitor of T-type calcium channels that blocks Cav3.1 in stably expressing HEK293 cells (IC50 = 6.8 ?M) with no discernible effect on high voltage-activated (L-type) channels in INS-1 cells up to a concentration of 100 ?M.{34694} NNC 55-0396 suppresses tremor in two murine models, the GABAA ?1-null (20 mg/kg) and harmaline-induced (12.5 mg/kg) tremor models, and was better tolerated than mibefradil (Item No. 15037).{34695} In arterial smooth muscle cells, NCC 55-0396 (IC50 = 80 nM) inhibits voltage-dependent K+ channels but does not affect their voltage sensitivity.{34696} NNC 55-0396 (1-5 ?M) also suppresses angiogenesis in vitro by inhibiting hypoxia-inducible factor-1? activity, and it slows tumor growth of flank xenografts of U87MG cells in mice when administered at 20 mg/kg.{34697}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • cyclopropanecarboxylic acid, (1S,2S)-2-[2-[[3-(1H-benzimidazol-2-yl)propyl]methylamino]ethyl]-6-fluoro-1,2,3,4-tetrahydro-1-(1-methylethyl)-2-naphthalenyl ester, dihydrochloride
  • Correlated keywords
    • 357400-14-7 HEK-293 NNC550396 NNC-550396 INS1 GABA-A a1 HIF-1? HIF1? 1a gamma?aminobutyric aminobutyrate
  • Product Overview:
    NNC 55-0396 is a selective inhibitor of T-type calcium channels that blocks Cav3.1 in stably expressing HEK293 cells (IC50 = 6.8 ?M) with no discernible effect on high voltage-activated (L-type) channels in INS-1 cells up to a concentration of 100 ?M.{34694} NNC 55-0396 suppresses tremor in two murine models, the GABAA ?1-null (20 mg/kg) and harmaline-induced (12.5 mg/kg) tremor models, and was better tolerated than mibefradil (Item No. 15037).{34695} In arterial smooth muscle cells, NCC 55-0396 (IC50 = 80 nM) inhibits voltage-dependent K+ channels but does not affect their voltage sensitivity.{34696} NNC 55-0396 (1-5 ?M) also suppresses angiogenesis in vitro by inhibiting hypoxia-inducible factor-1? activity, and it slows tumor growth of flank xenografts of U87MG cells in mice when administered at 20 mg/kg.{34697}

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