ChemicalBook--->CAS DataBase List--->49697-38-3

49697-38-3

49697-38-3 Structure

49697-38-3 Structure
IdentificationBack Directory
[Name]

RIMEXOLONE (100 MG)
[CAS]

49697-38-3
[Synonyms]

Vexol
Rimexel
Org-6216
Rimexolone
Rimexolone D5
Rimexolone D6
(11β,16α,17β)-
RIMEXOLONE (100 MG)
Rimexolone (1604600)
Benzoyl Peroxide Impurity 9
Methylprednisolone Impurity 31 (Rimexolone)
11β-Hydroxy-16α,17α-dimethyl-17β-propionylandrosta-1,4-dien-3-one
(17S)-11β-Hydroxy-16α,17α-dimethyl-17-(1-oxopropyl)androsta-1,4-dien-3-one
(11b,16a,17b)-11-Hydroxy-16,17-dimethyl-17-(1-oxopropyl)androsta-1,4-dien-3-one
(11β, 16α, 17β)-11-Hydroxy-16,17-dimethyl-17-(1-oxopropyl)androstra-1,4-dien-3-one
Androsta-1,4-dien-3-one, 11-hydroxy-16,17-dimethyl-17-(1-oxopropyl)-, (11β,16α,17β)-
[Molecular Formula]

C24H34O3
[MDL Number]

MFCD00866123
[MOL File]

49697-38-3.mol
[Molecular Weight]

370.52
Chemical PropertiesBack Directory
[Melting point ]

258-268 ºC
[alpha ]

D +100° (c = 0.92 in pyridine)
[Boiling point ]

507.0±50.0 °C(Predicted)
[density ]

1.12
[pka]

14.42±0.70(Predicted)
[InChIKey]

QTTRZHGPGKRAFB-OOKHYKNYSA-N
Safety DataBack Directory
[HS Code ]

2937290000
Hazard InformationBack Directory
[Description]

Rimexolone, an ophthalmic corticosteroid, was launched in 1995 in the U.S.A. for the treatment of postoperative inflammation following ocular surgery and anterior uveitis. Rimexolone has high corticoid receptor affinity and is a potent local antiinflammatory agent with minimal systemic effects and virtually no atrophogenic action in many animal models studied, unique among a wide range of topical steroids. Rapid onset, long duration of action plus a superior safety profile are characteristics of rimexolone. It was also approved in Europe for the treatment of rheumatoid arthritis and is currently in clinical trials for tendinitis and osteoarthritis.
[Originator]

Akzo (Netherlands)
[Uses]

Anti-inflammatory (local).
[Definition]

ChEBI:Rimexolone is a 20-oxo steroid.
[Brand name]

Vexol (Alcon).
[General Description]

Rimexolone, 11β-hydroxy-16α,17α-dimethyl-17-(1-oxopropyl)androsta-1,4-diene-3-one,like medrysone and fluorometholone, lacks the C21 OHgroup. In addition, rimexolone has an additional methylgroup in the 17 -position, a site where an OH group is typicallyfound. Rimexolone is available as a suspension forophthalmic use.
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