Description
A selective inhibitor of T-type calcium channels (IC50 = 6.8 μM); exhibits no activity against L-type calcium channels up to 100 μM; inhibits tremor in mice (20 mg/kg and 12.5 mg/kg in GABAA α1-null and harmaline-induced tremor models, respectively); inhibits Kv channels (IC50 = 80 nM)
Formal name: 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
Synonyms:
Molecular weight: 564.6
CAS: 357400-13-6
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Ion Channel Modulation|Blockers||Research Area|Cancer|Angiogenesis||Research Area|Cancer|Transcription Factors|HIF-1α||Research Area|Cancer|Tumor Microenvironment||Research Area|Cardiovascular System|Vasculature|Smooth Muscle Cells||Research Area|Cell Biology|Cell Signaling|Calcium Mobilization||Research Area|Neuroscience