| Weight | 370.533 g/mol |
|---|---|
| Formula | C24H34O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
RIMEXOLONE (49697-38-3)
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- Intraocular Pressure-Raising Potential of 1.0% Rimexolone in Patients Responding to Corticosteroids (Archives of Ophthalmology, 1996)
- Efficacy and Safety of Rimexolone 1 % Ophthalmic Suspension vs 1% Prednisolone Acetate in the Treatment of Uveitis (American Journal of Ophthalmology, 1996)
- Control of ocular inflammation after cataract extraction with rimexolone 1% ophthalmic suspension (Journal of Cataract and Refractive Surgery, 1997)
- Comparison of ketorolac tromethamine 0.5% and rimexolone 1% to control inflammation after cataract extraction : Prospective randomized double-masked study (Journal of Cataract and Refractive Surgery, 2001)
- Ocular-Hypertensive and Anti-inflammatory Response to Rimexolone Therapy in Children (Archives of Ophthalmology, 2003)
- The effects of Rimexolone 1% in postoperative inflammation after cataract extraction. A double-masked placebo-controlled study. (European Journal of Ophthalmology, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC(=O)C1(C(CC2C1(CC(C3C2CCC4=CC(=O)C=CC34C)O)C)C)C
-
InChIKeyQTTRZHGPGKRAFB-UHFFFAOYSA-N
- Pubchem - RIMEXOLONE
- Wikipedia - Rimexolone
Rimexolone is a glucocorticoid steroid used to treat inflammation in the eye. It is marketed as a 1% eye drop suspension under the trade name Vexol by Alcon Laboratories, but was discontinued in the US and other countries.
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