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Merck

B112

(±)-Bay K8644

≥97.5% (HPLC), Calcium channel agonist, powder

Sinonimo/i:

1,4-Dihydro-2,6-dimethyl-5-nitro-4-(2-[trifluoromethyl]phenyl)pyridine-3-carboxylic acid methyl ester

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5 MG

CHF 327.00

25 MG

CHF 1’310.00

CHF 327.00

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Informazioni su questo articolo

Formula empirica (notazione di Hill):
C16H15F3N2O4
Numero CAS:
71145-03-4
Peso molecolare:
356.30
UNSPSC Code:
12352202
PubChem Substance ID:
24277825
NACRES:
NA.77
MDL number:
MFCD00036697

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Nome del prodotto

(±)-Bay K8644, calcium channel agonist

SMILES string

CC1=C(C(OC)=O)C(C2=CC=CC=C2C(F)(F)F)C([N+]([O-])=O)=C(C)N1

InChI key

ZFLWDHHVRRZMEI-UHFFFAOYSA-N

InChI

1S/C16H15F3N2O4/c1-8-12(15(22)25-3)13(14(21(23)24)9(2)20-8)10-6-4-5-7-11(10)16(17,18)19/h4-7,13,20H,1-3H3

assay

≥97.5% (HPLC)

form

powder

color

yellow to dark yellow

mp

168-170  °C

solubility

DMSO: 20 mg/mL, methanol and ethanol: 63 mg/mL, H2O: insoluble

storage temp.

2-8°C

Quality Level

100

Gene Information

rat ... Cacna1c(24239)

Categorie correlate

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Questo articolo
B133SML1903SML1268
(±)-Bay K8644 calcium channel agonist

Sigma-Aldrich

B112

(±)-Bay K8644

(S)-(−)-Bay K8644 ≥98% (HPLC), solid

Sigma-Aldrich

B133

(S)-(−)-Bay K8644

IMB5046 ≥98% (HPLC)

Sigma-Aldrich

SML1903

IMB5046

BQU57 ≥98% (HPLC)

Sigma-Aldrich

SML1268

BQU57

assay

≥97.5% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

Gene Information

rat ... Cacna1c(24239)

Gene Information

human ... ADORA3(140)
rat ... Adora1(29290), Adora2a(25369)

Gene Information

-

Gene Information

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

powder

form

solid

form

powder

form

powder

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

solubility

DMSO: 20 mg/mL, H2O: insoluble, methanol and ethanol: 63 mg/mL

solubility

H2O: slightly soluble, ethanol: soluble (Organic solutions are stable for at least 20 days at RT.)

solubility

DMSO: 20 mg/mL, clear

solubility

DMSO: 25 mg/mL, clear

Application

(±)-Bay K8644 has been used as an agonist for voltage sensitive calcium channels (VSCCs) in interneurons,[1] L-type calcium channel (LTCC) in human embryonic kidney 293 cells[2] and viscerofugal neurons.[3]

Biochem/physiol Actions

(±)-Bay K8644 is a 1,4-dihydropyridine (DHP) derivative and an agonist for L-type Ca2+ channels.[4] However, it′s enantiomers (-)-BAY k8644 and (+)-BAY k8644 have opposing functionality with respect to Ca2+ channels as high-potency agonist and low-potency antagonist, respectively.[5] (±)-Bay K8644 increases influx of Ca2+ specifically at voltage-gated calcium channels. It constricts blood vessels and heart contraction.[6]
Increases influx of Ca2+ specifically at voltage-gated calcium channels.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Classe di stoccaggio

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
0000525274
0000525274
0000449374
0000449374
0000361440

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CaV1.2 channelopathic mutations evoke diverse pathophysiological mechanisms.
Bamgboye, et al.
The Journal of General Physiology, 154 (2023)
Opposing actions of Bay K 8644 enantiomers on calcium current, prolactin secretion, and synthesis in pituitary cells
Enyeart JJ, et al.
Molecular Endocrinology, 4(5), 727-735 (1990)
Diego Santos de Souza et al.
European journal of pharmacology, 859, 172488-172488 (2019-06-25)
Cardiac arrhythmias are among the most important pathologies that lead to sudden death. The discovery of new therapeutic options against arrhythmias with low adverse effects is of paramount importance. Farnesol is found in essential oils with antioxidant, anti-inflammatory and cardioprotective
Spectrum of Cav1. 4 dysfunction in congenital stationary night blindness type 2
Burtscher V, et al.
Biochimica et Biophysica Acta, 1838(8), 2053-2065 (2014)
The calcium channel agonist BAY k 8644 reduces ethanol intake and preference in alcohol-preferring AA rats
de Beun R, et al.
Psychopharmacology, 127(1-2), 302-310 (1996)
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