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ChemicalBook--->CAS DataBase List--->265989-46-6

265989-46-6

265989-46-6 Structure

265989-46-6 Structure
IdentificationBack Directory
[Name]

di(2-Hydroxy Atorvastatin) CalciuM Salt
[CAS]

265989-46-6
[Synonyms]

Atorvastatin Impurity K
2-Hydroxy Atorvastatin Sodium
2-Hydroxy Atorvastatin CalciuM Salt
di(2-Hydroxy Atorvastatin) CalciuM Salt
calcium,(3S,5S)-7-[2-(4-fluorophenyl)-4-[(2-hydroxyphenyl)carbamoyl]-3-phenyl-5-propan-2-ylpyrrol-1-yl]-3,5-dihydroxyheptanoate
Atorvastatin impurity 39/Atorvastatin 2-Hydroxy Calcium Salt/ortho-Hydroxy Atorvastatin Calcium Salt/(3R,5R)-7-[3-(2-Hydroxyphenylcarbamoyl)-5-(4-fluorophenyl)-2-isopropyl-4-phenyl-1H-pyrrol-1-yl]-3,5-dihydroxyheptanoic acid calcium salt
[Molecular Formula]

C33H37CaFN2O6
[MDL Number]

MFCD08063637
[MOL File]

265989-46-6.mol
[Molecular Weight]

616.74
Chemical PropertiesBack Directory
[Melting point ]

>166°C (dec.)
[storage temp. ]

Hygroscopic, Refrigerator, under inert atmosphere
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Yellow
[Stability:]

Hygroscopic
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
Hazard InformationBack Directory
[Chemical Properties]

White to Pale Yellow Solid
[Uses]

di(2-Hydroxy Atorvastatin) Calcium Salt is a metabolite of Atorvastatin Calcium Salt (A791750), a selective, competitive HMG-CoA reductase inhibitor. Atorvastatin is the only drug in its class specfically indicated for lowering both elevated LDL-cholesterol and triglycerides in patients with hypercholesterolemia.
[Biological Activity]

2-Hydroxy atorvastatin calcium salt is a hydroxy metabolite of Atorvastatin calcium salt. Atorvastatin is a potent HMG-CoA reductase inhibitor with an IC50 value of 8 nM. It inhibits lipid hydroperoxide formation and copper sulfate-induced thiobarbituric acid reactive substances (TBARS) formation in 1,2-dilinoleoyl-sn-glycero-3-PC (DLPC) vesicles and human LDL, respectively, in a concentration-dependent manner. 2-Hydroxy Atorvastatin reduces cell death induced by oxygen-glucose deprivation (OGD) in primary rat cortical neurons and increases phosphorylation of cAMP-response-element-binding protein (CREB) in GABAergic neurons when used at a concentration of 600 nM following OGD.
[storage]

Store at -20°C
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