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ChemicalBook--->CAS DataBase List--->265989-50-2

265989-50-2

265989-50-2 Structure

265989-50-2 Structure
IdentificationBack Directory
[Name]

2-Hydroxy Atorvastatin Lactone-d5
[CAS]

265989-50-2
[Synonyms]

2-Hydroxy Atorvastatin Lactone-d5
[2H5]-2-Hydroxy Atorvastatin Lactone
5-(4-fluorophenyl)-1-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-N-(2-hydroxyphenyl)-4-(2,3,4,5,6-pentadeuteriophenyl)-2-propan-2-ylpyrrole-3-carboxamide
5-(4-Fluorophenyl)-N-(2-hydroxyphenyl)-2-(1-Methylethyl)-4-phenyl-1-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1H-pyrrole-3-carboxaMide-d5
1H-Pyrrole-3-carboxamide, 5-(4-fluorophenyl)-N-(2-hydroxyphenyl)-2-(1-methylethyl)-4-(phenyl-d5)-1-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]- (9CI)
[Molecular Formula]

C33H33FN2O5
[MDL Number]

MFCD08063402
[MOL File]

265989-50-2.mol
[Molecular Weight]

556.624
Chemical PropertiesBack Directory
[Melting point ]

103-107°C
[storage temp. ]

Hygroscopic, -20°C Freezer, Under Inert Atmosphere
[solubility ]

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

Solid
[color ]

Pale Yellow to Beige
[Stability:]

Hygroscopic
Hazard InformationBack Directory
[Chemical Properties]

Yellow Solid
[Uses]

An isotopically labelled metabolite of Atorvastin, a selective, competitive HMG-CoA reductase inhibitor. Atorvastin is the only drug in its class specfically indicated for lowering both elevated LDL-cholesterol and triglycerides in patients with hypercholesterolemia.
[References]

[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Guo CX, et al. Effects of Ginkgo biloba extracts on pharmacokinetics and efficacy of atorvastatin based on plasma indices. Xenobiotica. 2012;42(8):784‐790. DOI:10.3109/00498254.2012.661100
[3] Turner NA, et al. Comparison of the efficacies of five different statins on inhibition of human saphenous vein smooth muscle cell proliferation and invasion. J Cardiovasc Pharmacol. 2007 Oct;50(4):458-61. DOI:10.1097/FJC.0b013e318123767f
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