ChemicalBook--->CAS DataBase List--->1257116-00-9

1257116-00-9

1257116-00-9 Structure

1257116-00-9 Structure
IdentificationBack Directory
[Name]

RQ-00311651
[CAS]

1257116-00-9
[Synonyms]

RQ-00311651
[Molecular Formula]

C19H18F3N5O2
[MOL File]

1257116-00-9.mol
[Molecular Weight]

405.37
Chemical PropertiesBack Directory
[Boiling point ]

655.8±55.0 °C(Predicted)
[density ]

1.425±0.06 g/cm3(Predicted)
[pka]

11.95±0.10(Predicted)
Hazard InformationBack Directory
[Description]

RQ-00311651 is a novel T-type Ca2+ channel blocker, in distinct rodent models for neuropathic and visceral pain. RQ-00311651 strongly suppressed T currents when tested at holding potentials of -65 ~ -60 mV, but not -80 mV, in the Cav3.1- or Cav3.2-expressing cells. RQ-00311651 also inhibited high K-induced Ca signaling in those cells.
[Uses]

RQ-00311651 is a T-type calcium channel blocker that specifically targets the Cav3.2 isoform with a role in neuropathic and visceral pain. RQ-00311651 significantly inhibits T currents in HEK293 cells expressing human Cav3.1 or Cav3.2. RQ-00311651 also inhibited high potassium-induced calcium signaling. RQ-00311651 also inhibits antiallergic properties in rats and mice with neuropathic pain induced by spinal nerve injury or Paclitaxel (HY-B0015). Oral and intraperitoneal injection (10-20 mg/kg) inhibits Cerulein (HY-A0190)-induced acute pancreatitis and cyclophosphamide-induced cystitis in mice[1].
[References]

[1] Therapeutic potential of RQ-00311651, a novel T-type Ca2+ channel blocker, in distinct rodent models for neuropathic and visceral pain
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