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(S)-(−)-Bay K8644

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For Research Use Only | Not For Clinical Use
CATAP98625264
CAS98625-26-4
MDL NumberMFCD00153769
Molecular Weight356.30
InChI KeyZFLWDHHVRRZMEI-ZDUSSCGKSA-N
Description≥98% (HPLC), solid
SolubilityH2O: slightly soluble; ethanol: soluble (Organic solutions are stable for at least 20 days at RT.)
Assay≥98% (HPLC)
Coloryellow
Formsolid
Size1MG, 5MG
Storage Conditions2-8°C
1

Calcium Channel Agonist, (+/-)-Bay K8644, Causes a Transient Increase in Striatal Monoamine Oxidase Activity in Balb/c Mice

Supriti Samantaray, Goutam Chandra, Kochupurackal P Mohanakumar

Neurosci Lett. 2003 May 15;342(1-2):73-6.

PMID: 12727321

1

Calcium Channel Agonist, (+/-)-Bay K8644, Causes an Immediate Increase in the Striatal 1-methyl-4-phenylpyridinium Level Following Systemic Administration of the Dopaminergic Neurotoxin, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, in Balb/c Mice

Supriti Samantaray, Kochupurackal P Mohanakumar

Neurosci Lett. 2003 Jul 31;346(1-2):69-72.

PMID: 12850550

1

Effects of Calcium Channel Activators BAY-K8644 and CGP-28392 on Steroidogenesis in Granulosa Cells of the Domestic Hen

E K Asem, B K Tsang

Biochem Biophys Res Commun. 1987 Jul 15;146(1):314-20.

PMID: 2440434

1

Effects of the Ca Agonist Bay K8644 on 45Ca Influx and Net Ca Uptake Into Rabbit Aortic Smooth Muscle

K S Hwang, C Van Breemen

Eur J Pharmacol. 1985 Oct 22;116(3):299-305.

PMID: 2416574

1

Maturation of Rat Cerebellar Purkinje Cells Reveals an Atypical Ca2+ Channel Current That Is Inhibited by Omega-Agatoxin IVA and the Dihydropyridine (-)-(S)-Bay K8644

Elizabeth W Tringham, C Elizabeth Payne, Jonathan R B Dupere, Maria M Usowicz

J Physiol. 2007 Feb 1;578(Pt 3):693-714.

PMID: 17124267

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