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BAY K 8644, S(−)- (CAS 98625-26-4)

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Alternate Names:
(S)-(−)-Bay K 8644
Application:
BAY K 8644, S(−)- is an L-type Ca2+-channel activator
CAS Number:
98625-26-4
Purity:
≥99%
Molecular Weight:
356.3
Molecular Formula:
C16H15F3N2O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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BAY K 8644, specifically the S(−)-enantiomer, is a potent chemical modulator of calcium channels, primarily targeting the L-type calcium channels which are for the regulation of calcium influx in various cell types. This compound acts as an agonist, enhancing the channel′s opening probability, which leads to an increased intracellular calcium concentration. The mechanism by which BAY K 8644 exerts its effect involves binding to the channel in a state-dependent manner, preferentially associating with and stabilizing the open state of the channel. This unique action makes it an invaluable tool in research, especially in studies aimed at understanding the physiological and pathological roles of L-type calcium channels in cellular processes. Through its ability to modulate calcium dynamics precisely, BAY K 8644 has facilitated the exploration of calcium′s pivotal role in signaling pathways, cellular contraction, and secretion processes, thereby contributing significantly to the advancement of cellular and molecular biology research fields. When used in conjunction with BIX01294, BAY K 8644, S(−)- facilitates the reprogramming of mouse embryonic fibroblasts following transduction with Oct4/Klf4.5. BAY K 8644, S(−)- is specifically methyl 2,6-dimethyl-5-nitro-4-[2-(trifluoromethyl)phenyl]-1,4-dihydropyridine-3-carboxylate, with an (S)-configuration at the 4-position.


BAY K 8644, S(−)- (CAS 98625-26-4) References

  1. Preferential action of gabapentin and pregabalin at P/Q-type voltage-sensitive calcium channels: inhibition of K+-evoked [3H]-norepinephrine release from rat neocortical slices.  |  Dooley, DJ., et al. 2002. Synapse. 45: 171-90. PMID: 12112396
  2. Effects of the enantiomers of BayK 8644 on the charge movement of L-type Ca channels in guinea-pig ventricular myocytes.  |  Artigas, P., et al. 2003. J Membr Biol. 193: 215-27. PMID: 12962282
  3. Comparison of the effects of BAY K 8644 on cardiac Ca2+ current and Ca2+ channel gating current.  |  Hadley, RW. and Lederer, WJ. 1992. Am J Physiol. 262: H472-7. PMID: 1371650
  4. L-type Ca2+ channels contribute to current-evoked spike firing and associated Ca2+ signals in cerebellar Purkinje neurons.  |  Gruol, DL., et al. 2006. Cerebellum. 5: 146-54. PMID: 16818389
  5. Opposite cardiac actions of the enantiomers of Bay K 8644 at different membrane potentials in guinea-pig papillary muscles.  |  Ravens, U. and Schöpper, HP. 1990. Naunyn Schmiedebergs Arch Pharmacol. 341: 232-9. PMID: 1692975
  6. The effects of strychnine on the regulation of voltage-dependent calcium channels by dihydropyridines in brain and heart.  |  O'Neill, SK. and Bolger, GT. 1990. Pharmacol Biochem Behav. 35: 833-40. PMID: 1693213
  7. Characterization of the relaxant response to N,N'-dipropyl-1,2-bis(2,6-dichloro-4-hydroxyphenyl)ethylenediamine in porcine coronary arteries.  |  Moritz, A., et al. 2007. J Pharmacol Exp Ther. 321: 699-706. PMID: 17322023
  8. Citral sensing by Transient [corrected] receptor potential channels in dorsal root ganglion neurons.  |  Stotz, SC., et al. 2008. PLoS One. 3: e2082. PMID: 18461159
  9. Cardamonin is a bifunctional vasodilator that inhibits Ca(v)1.2 current and stimulates K(Ca)1.1 current in rat tail artery myocytes.  |  Fusi, F., et al. 2010. J Pharmacol Exp Ther. 332: 531-40. PMID: 19923439
  10. Failure of Bay K 8644 to induce RhoA kinase-dependent calcium sensitization in rabbit blood vessels.  |  Alvarez, SM., et al. 2010. Br J Pharmacol. 160: 1326-37. PMID: 20590624
  11. Pharmacological profile of 2-bromoterguride at human dopamine D2, porcine serotonin 5-hydroxytryptamine 2A, and α2C-adrenergic receptors, and its antipsychotic-like effects in rats.  |  Jantschak, F., et al. 2013. J Pharmacol Exp Ther. 347: 57-68. PMID: 23863695
  12. The optical isomers of the 1,4-dihydropyridine BAY K 8644 show opposite effects on Ca channels.  |  Franckowiak, G., et al. 1985. Eur J Pharmacol. 114: 223-6. PMID: 2412855
  13. Enantiomer selectivity and the development of tolerance to the behavioral effects of the calcium channel activator BAY K 8644.  |  O'Neill, SK. and Bolger, GT. 1988. Brain Res Bull. 21: 865-72. PMID: 2465070
  14. Calcium Channel Blocker Nifedipine Suppresses Colorectal Cancer Progression and Immune Escape by Preventing NFAT2 Nuclear Translocation.  |  Wu, L., et al. 2020. Cell Rep. 33: 108327. PMID: 33113363
  15. The amyloid beta-protein of Alzheimer's disease increases acetylcholinesterase expression by increasing intracellular calcium in embryonal carcinoma P19 cells.  |  Sberna, G., et al. 1997. J Neurochem. 69: 1177-84. PMID: 9282941

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

BAY K 8644, S(−)-, 10 mg

sc-203525
10 mg
$398.00

BAY K 8644, S(−)-, 50 mg

sc-203525A
50 mg
$1428.00