FPL64176

CAS No. 120934-96-5

FPL64176( ARC-64176 | FPL-64176 )

Catalog No. M10781 CAS No. 120934-96-5

FPL64176 (ARC-64176) is a potent L-type Ca++ channel activator with EC50 of 16 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 72 Get Quote
10MG 115 Get Quote
25MG 250 Get Quote
50MG 462 Get Quote
100MG 672 Get Quote
500MG 1404 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    FPL64176
  • Note
    Research use only, not for human use.
  • Brief Description
    FPL64176 (ARC-64176) is a potent L-type Ca++ channel activator with EC50 of 16 nM.
  • Description
    FPL64176 (ARC-64176) is a potent L-type Ca++ channel activator with EC50 of 16 nM; prolongs action potential duration and enhances contractility in guinea pig papillary muscle, induces contractile response with EC50 of 0.2 uM; produces biexponential tail current decays at -50 mV with fast and slow time constants of 4.30 +/- 0.30 and 44.52 +/- 4.56 msec, respectively; produces large increases in cardiac contractile force and diastolic blood pressure in anesthetized dogs (100 mg/kg, i.v.). Heart Failure Discontinued.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ARC-64176 | FPL-64176
  • Pathway
    GPCR/G Protein
  • Target
    Calcium Channel
  • Recptor
    Calcium Channel
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    120934-96-5
  • Formula Weight
    347.414
  • Molecular Formula
    C22H21NO3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (287.84 mM)
  • SMILES
    O=C(C1=C(C)NC(C)=C1C(C2=CC=CC=C2CC3=CC=CC=C3)=O)OC
  • Chemical Name
    2,5-Dimethyl-4-[2-(phenylmethyl)benzoyl]-1H-pyrrole-3-carboxylic acid methyl ester

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Baxter AJ, et al. J Med Chem. 1993 Sep 17;36(19):2739-44. 2. Rampe D, et al. J Pharmacol Exp Ther. 1993 Jun;265(3):1125-30. 3. Zheng W, et al. Mol Pharmacol. 1991 Nov;40(5):734-41. 4. Liu L, et al. Neuropharmacology. 2003 Aug;45(2):281-92.
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