| Weight | 255.273 g/mol |
|---|---|
| Formula | C15H13NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
ketorolac (66635-83-4, 74103-06-3)
Score:
#415 in Neuroscience
,
#1908 in Biology
,
#2307 in Chemistry
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- Ketorolac: A Review of its Pharmacodynamic and Pharmacokinetic Properties, and Therapeutic Potential (Drugs, 1990)
- Risk of hospitalization for upper gastrointestinal tract bleeding associated with ketorolac, other nonsteroidal anti-inflammatory drugs, calcium antagonists, and other antihypertensive drugs. (JAMA Internal Medicine, 1998)
- Parenteral Ketorolac and Risk of Gastrointestinal and Operative Site Bleeding: A Postmarketing Surveillance Study (JAMA, 1996)
- Pharmacology of the Spinal Action of Ketorolac, Morphine, ST-91, U50488H, and L-PIA on the Formalin Test and an Isobolographic Analysis of the NSAID Interaction (Anesthesiology, 1993)
- Ketorolac : A reappraisal of its pharmacodynamic and pharmacokinetic properties and therapeutic use in pain management (Drugs, 1997)
- Semi-interpenetrating polymer network microspheres of gelatin and sodium carboxymethyl cellulose for controlled release of ketorolac tromethamine (Carbohydrate Polymers, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CN2C(=CC=C2C(=O)C3=CC=CC=C3)C1C(=O)O
-
InChIKeyOZWKMVRBQXNZKK-UHFFFAOYSA-N
- Pubchem - ketorolac
- Wikipedia - ketorolac
Ketorolac, sold under the brand name Toradol among others, is a nonsteroidal anti-inflammatory drug (NSAID) in the family of heterocyclic acetic acid derivatives, used as an analgesic. It is considered a first-generation NSAID. Ketorolac acts by inhibiting the bodily synthesis of prostaglandins.
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