Date published: 2025-11-22

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Nemadipine-B (CAS 79925-38-5)

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Alternate Names:
Felodipine Diethyl Ester
Application:
Nemadipine-B is a cell permeable L-type calcium channel protein inhibitor
CAS Number:
79925-38-5
Molecular Weight:
398.3
Molecular Formula:
C19H21Cl2NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Nemadipine-A is a cell permeable L-type calcium channel protein inhibitor in C. elegans.


Nemadipine-B (CAS 79925-38-5) References

  1. A small-molecule screen in C. elegans yields a new calcium channel antagonist.  |  Kwok, TC., et al. 2006. Nature. 441: 91-5. PMID: 16672971
  2. Synthesis, Biological Evaluation and Molecular Docking Studies of Novel Di-hydropyridine Analogs as Potent Antioxidants.  |  Sudhana, SM. and Adi, PJ. 2019. Curr Top Med Chem. 19: 2676-2686. PMID: 31702500
  3. Automated Functional Screening for Modulators of Optogenetically Activated Neural Responses in Living Organisms.  |  Lagoy, RC., et al. 2021. Methods Mol Biol. 2191: 221-233. PMID: 32865748
  4. A Highly Chemically Robust 3D Interpenetrated MOF Heterogeneous Catalyst for the Synthesis of Hantzsch 1,4-Dihydropyridines and Drug Molecules.  |  Sahoo, R., et al. 2024. Small. 20: e2309281. PMID: 38191986
  5. Facile One-Pot Synthesis and Anti-Microbial Activity of Novel 1,4-Dihydropyridine Derivatives in Aqueous Micellar Solution under Microwave Irradiation.  |  Goswami, A., et al. 2024. Molecules. 29: PMID: 38474626
  6. A new In–SiO 2 composite catalyst in the solvent-free multicomponent synthesis of Ca 2+ channel blockers nifedipine and nemadipine B.  |  Affeldt, Ricardo F., et al. 2012. New Journal of Chemistry. 36.7: 1502-1511.
  7. Light induced synthesis of symmetrical and unsymmetrical dihydropyridines in ethyl lactate–water under tunable conditions.  |  Ghosh, Partha Pratim, et al. 2013. Tetrahedron Letters. 54.2: 138-142.
  8. L-Proline catalyzed synthesis of structurally diverse 1, 4-dihydropyridines fused with medicinally privileged heterocyclic systems.  |  Khandelwal, Sarita, et al. 2014. Current Organocatalysis. 1.1: 51-58.
  9. First report about the use of micellar keggin heteropolyacids as catalysts in the green multicomponent synthesis of nifedipine derivatives.  |  Palermo, Valeria, et al. 2016. Catalysis Letters. 146: 1634-1647.
  10. Mechanochemical enzymatic synthesis of 1, 4‐dihydropyridine calcium antagonists and derivatives.  |  Jiang, Ling, et al. 2019. Journal of Chemical Technology & Biotechnology. 94.8: 2555-2560.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Nemadipine-B, 10 mg

sc-203157
10 mg
$275.00