Grundinformationen
- Standard-SMILES
CC(C)c1c(C(=O)Nc2ccccc2)c(-c2ccccc2)c(-c2ccc(F)cc2)n1CC[C@@H]1C[C@@H](O)CC(=O)O1- InChIKey
OUCSEDFVYPBLLF-KAYWLYCHSA-N- Summenformel
- C33H33FN2O4
- Durchschnittliche Molmasse
- 540,6 g/mol
- Monoisotopische Masse
- 540,24243576
Überblick
Atorvastatin lactone is a member of pyrroles.
Namen und Bezeichner
- Bevorzugter Name
- Atorvastatin lactone
- IUPAC
- 5-(4-fluorophenyl)-1-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-N,4-diphenyl-2-propan-2-ylpyrrole-3-carboxamide
- Englischer Name
- Atorvastatin lactone
- Summenformel
- C33H33FN2O4
- Molmasse
- 540.62
Namen und Synonyme
Atorvastatin lactone125995-03-1Atorvastatin delta-LactoneUNII-7876IL7J2N7876IL7J2N1H-Pyrrole-3-carboxamide, 5-(4-fluorophenyl)-2-(1-methylethyl)-N,4-diphenyl-1-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-DTXSID901550331H-Pyrrole-3-carboxamide, 5-(4-fluorophenyl)-2-(1-methylethyl)-N,4-diphenyl-1-(2-((2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl)ethyl)-1H-PYRROLE-3-CARBOXAMIDE, 5-(4-FLUOROPHENYL)-2-(1-METHYLETHYL)-N,4-DIPHENYL-1-(2-(TETRAHYDRO-4-HYDROXY-6-OXO-2H-PYRAN-2-YL)ETHYL)-, (2R-TRANS)-1H-Pyrrole-3-carboxamide, 5-(4-fluorophenyl)-2-(1-methylethyl)-N,4-diphenyl-1-[2-(tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl)ethyl]-, (2R-trans)-5-(4-FLUOROPHENYL)-1-(2-((2R,4R)-4-HYDROXY-6-OXOTETRAHYDROPYRAN-2-YL)ETHYL)-2-ISOPROPYL-4-PHENYL-1H-PYRROLE-3-CARBOXYLIC ACID PHENYLAMIDE5-(4-fluorophenyl)-1-[2-[(2r,4r)-4-hydroxy-6-oxotetrahydropyran-2-yl]ethyl]-2-isopropyl-4-phenyl-1h-pyrrole-3-carboxylic acid phenylamide
Weitere Namen anzeigen
Atorvastatin EP IMpurity HPD-130694Atorvastatin USP RC HAtorvastatin calcium-6Atorvastatin d-LactoneAtorvastatin Impurity HLACTONE IMPURITY(IMP-H)(RS) Atorvastatin Lactone
RefChem:5572DTXCID4077524(+)-ATORVASTATIN LACTONE418-950-3MFCD008992625-(4-fluorophenyl)-1-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-N,4-diphenyl-2-propan-2-ylpyrrole-3-carboxamide5-(4-Fluorophenyl)-2-(1-methylethyl)-N,4-diphenyl-1-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1H-pyrrole-3-carboxamideC33H33FN2O4
Datenbank-Bezeichner
- CAS
125995-03-1- PubChem CID
- 6483036
- DTXSID
DTXSID90155033- ChEMBL
CHEMBL333687- ChEBI
CHEBI:233896- UNII
- 7876IL7J2N
- EC Number
- 418-950-3、642-043-3
- Nikkaji
- J360.189G
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 5,7
- Polarare Oberfläche (TPSA)
- 80,6 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 5
- Frei drehbare Bindungen
- 8
- Schwere Atome
- 40
- Formalladung
- 0
- Komplexität
- 834
Experimentelle und physikochemische Eigenschaften
DrugsPharmaceuticals -> Metabolite of Atorvastatin
Physikochemische Eigenschaften
- Schmelzpunkt
- 103 · 103-106°C
- Siedepunkt
- 674.8 · 674.8±55.0 °C(Predicted)
- Dichte
- 1.24 · 1.24±0.1 g/cm3(Predicted)
- storage temp.
- 2 · Sealed in dry,2-8°C
- Löslichkeit
- Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
- pka
- 13.39 · 13.39±0.40(Predicted)
- Aggregatzustand
- Solid
- Farbe
- White to Light Yellow
- Merck
- 14 · 14,864
- Major Application
- pharmaceutical (small molecule)
- InChIKey
- OUCSEDFVYPBLLF-KAYWLYCHSA-N
- SMILES
- Fc1ccc(cc1)c2[n](c(c(c2c5ccccc5)C(=O)Nc4ccccc4)C(C)C)CC[C@H]3OC(=O)C[C@@H](C3)O
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
H413 (100%): May cause long lasting harmful effects to aquatic life [Hazardous to the aquatic environment, long-term hazard]
P273, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 29 reports by companies from 1 notifications to the ECHA C&L Inventory.
Warning
H302 (50%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P273, P301+P317, P330, and P501 (click each P-code to see the statement)
Gefahrenhinweise
Regulatory InformationStatus: Active Update: 15-12-2008 https://echa.europa.eu/registration-dossier/-/registered-dossier/9836
Hazard Classes and Categories
Aquatic Chronic 4 (100%)
Aquatic Chronic 4 (50%)
Sicherheitsdaten
- wgk
- WGK 3
- hs_code
- 2933.99.7500
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Anwendungen
VerwendenAtorvastatin intermediate as inhibitor of MAP kinase and/or HMG-CoA reductase for the treatment of inflammation
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