(+)-Ketorolac
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Grundinformationen
- CAS
66635-93-6- Standard-SMILES
O=C(c1ccccc1)c1ccc2n1CC[C@H]2C(=O)O- InChIKey
OZWKMVRBQXNZKK-LLVKDONJSA-N- Summenformel
- C15H13NO3
- Durchschnittliche Molmasse
- 255,273 g/mol
- Monoisotopische Masse
- 255,08954328
Namen und Bezeichner
- Bevorzugter Name
- (+)-Ketorolac
- IUPAC
- (1R)-5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid
- Englischer Name
- (R)-(+)-Ketorolac
- Summenformel
- C15H13NO3
- Molmasse
- 255.27
Namen und Synonyme
(1R)-5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid(+)-Ketorolac(R)-Ketorolac(R)-(+)-KetorolacKetorolac R-IsoMer(R)-Ketorolac, 10 mM in DMSO(R)-Ketorolac [(+)-Ketorolac)(R)-(+)-Ketorolac ISO 9001：2015 REACHKetorolac impurity 1/Ketorolac R-Isomer(R)-5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid
Datenbank-Bezeichner
- CAS
66635-93-6- PubChem CID
- 181818
- DTXSID
DTXSID801317579- ChEMBL
CHEMBL1619630- ChEBI
CHEBI:76227- UNII
- 10A5O25ILE
- EC Number
- 110-708-2
- Nikkaji
- J269.530H
Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 163 · 163-170°C
- storage temp.
- -20 °C · -20°C
- Löslichkeit
- Chloroform (Slightly), Methanol (Slightly)
- Aggregatzustand
- powder
- Farbe
- white to beige
- InChI
- 1S/C15H13NO3/c17-14(10-4-2-1-3-5-10)13-7-6-12-11(15(18)19)8-9-16(12)13/h1-7,11H,8-9H2,(H,18,19)/t11-/m1/s1
- InChIKey
- OZWKMVRBQXNZKK-LLVKDONJSA-N
- SMILES
- O=C(O)[C@H]1C2=CC=C(C(C3=CC=CC=C3)=O)N2CC1
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Sicherheitsdaten
- wgk
- WGK 3
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2STOT SE 3
Chemie und Industrie
Anwendungen
Verwenden(R)-Ketorolac is the R-enantiomer of Ketorolac. The (S)-enantiomer is about 60 times more potent than (R)-enantiomer. Prostaglandin biosynthesis inhibitor. Analgesic; anti-inflammatory.
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Ergänzende Hinweise
DefinitionChEBI: A 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid that has R configuration. Unlike the S-enantiomer, it does not exhibit COX1 and COX2 inhibition, but does exhibit analgesic activity. Racemic keto olac, known simply as ketorolac, is used (mainly as a tromethamine salt) as a potent analgesic for the short-term management of post-operative pain, and in eye drops to relieve the ocular itching associated with seasonal allergic conjunctivitis.
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