(-)-Ketorolac
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(-)-Ketorolac
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CAS No:
66635-92-5
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Formula:
C15H13NO3
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Chemical Name:
(-)-Ketorolac
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Synonyms:
1H-Pyrrolizine-1-carboxylic acid,5-benzoyl-2,3-dihydro-,(1S)-;1H-Pyrrolizine-1-carboxylic acid,5-benzoyl-2,3-dihydro-,(S)-;(1S)-5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid;S-(-)-Ketorolac;(S)-Ketorolac;(-)-Ketorolac
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CAS No:
Description
(S)-Ketorolac is a nonsteroidal anti-inflammatory agent. (S)-ketorolac exhibits potent COX1 and COX2 enzyme inhibition[1].
(S)-ketorolac is a 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid that has S configuration. While (S)-ketorolac is a COX1 and COX2 inhibitor, both enantiomers exhibit analgesic effects. Racemic ketorolac, known simply as ketorolac, is used (mainly as the 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. It has a role as an analgesic, a cyclooxygenase 2 inhibitor, a cyclooxygenase 1 inhibitor and a non-steroidal anti-inflammatory drug. It is an enantiomer of a (R)-ketorolac.
Characteristics
59.3
2.08
1.3±0.1 g/cm3
>250 °C
493.2±40.0 °C at 760 mmHg
252.1±27.3 °C
1.659
Refrigerator
(-)-Ketorolac Use and Manufacturing
The R-enantiomer of Ketorolac. The (S)-enantiomer is about 60 times more potent than (R)-enantiomer. Prostaglandin biosynthesis inhibitor. Analgesic; anti-inflammatory.
Computed Properties
Molecular Weight:255.27
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:255.08954328
Monoisotopic Mass:255.08954328
Topological Polar Surface Area:59.3
Heavy Atom Count:19
Complexity:376
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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