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BAY U6751 hydrate_Molecular_structure_CAS_114290-51-6(anhydrous))
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BAY U6751 hydrate

Catalog No. B3686 Name Sigma Aldrich
CAS Number 114290-51-6(anhydrous) Website http://www.sigmaaldrich.com
M. F. C20H22ClNNa2O7 Telephone 1-800-521-8956
M. W. 469.82372 Fax
Purity ≥98% (HPLC) Email
Storage protect from light Chembase ID: 153852

SYNONYMS

IUPAC name
disodium 4-(2-chlorophenyl)-1-ethyl-6-methyl-5-[(propan-2-yloxy)carbonyl]-1,4-dihydropyridine-2,3-dicarboxylate hydrate
IUPAC Traditional name
disodium 4-(2-chlorophenyl)-1-ethyl-5-(isopropoxycarbonyl)-6-methyl-4H-pyridine-2,3-dicarboxylate hydrate
Synonyms
4-(2-Chlorophenyl)-1-ethyl-1,4-dihydro-6-methyl-2,3,5-pyridinetricarboxylic acid 5-isopropyl ester disodium salt hydrate

DATABASE IDS

MDL Number MFCD08705410
CAS Number 114290-51-6(anhydrous)
PubChem SID 24891730

PROPERTIES

Empirical Formula (Hill Notation) C20H20ClNNa2O6 · xH2O
Purity ≥98% (HPLC)
Apperance white solid
Solubility H2O: >8 mg/mL
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
Storage Condition protect from light
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Caution
Light sensitive. Store in amber vials.
Biochem/physiol Actions
BAY W1807, the active metabolite of BAY R3401, inhibits muscle glycogen phosphorylase a and b. In gel-filtered liver extracts, racemic BAY U6751 (containing active BAY W1807) was tested for inhibition of phosphorylase in the glycogenolytic (in which only phosphorylase a is active). In liver extracts, BAY U6751 (0.9-36 μmol/L) inhibited glycogen synthesis by phosphorylase b (notwithstanding the inclusion of AMP), but not by phosphorylase a. Inhibition of phosphorylase-a-catalyzed glycogenolysis was partially relieved by AMP (500 μmol/L). BAY U6751 facilitated phosphorylase-a dephosphorylation. Isolated hepatocytes and perfused livers were tested for BAY R3401-induced changes in phosphorylase-a:b ratios and glycogenolytic output.
Description (简体中文)
Caution
Light sensitive. Store in amber vials.
Biochem/physiol Actions
BAY W1807, the active metabolite of BAY R3401, inhibits muscle glycogen phosphorylase a and b. In gel-filtered liver extracts, racemic BAY U6751 (containing active BAY W1807) was tested for inhibition of phosphorylase in the glycogenolytic (in which only phosphorylase a is active). In liver extracts, BAY U6751 (0.9-36 μmol/L) inhibited glycogen synthesis by phosphorylase b (notwithstanding the inclusion of AMP), but not by phosphorylase a. Inhibition of phosphorylase-a-catalyzed glycogenolysis was partially relieved by AMP (500 μmol/L). BAY U6751 facilitated phosphorylase-a dephosphorylation. Isolated hepatocytes and perfused livers were tested for BAY R3401-induced changes in phosphorylase-a:b ratios and glycogenolytic output.

REFERENCES