Name | parecoxib |
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Synonyms |
N-{[4-(5-Methyl-3-phenyl-1,2-oxazol-4-yl)phenyl]sulfonyl}propanamide
N-[[4-[5-methyl-3-phenylisoxazol-4-yl]phenyl]sulfonyl]propanamide parecoxib N-[[4-(5-methyl-3-phenyl-4-isoxazolyl)phenyl]sulfonyl]-propanamide 4-[4-(N-propionylsulfamoyl)-phenyl]-5-methyl-3-phenyl-isoxazole N-propanoyl-4-(5-methyl-3-phenylisoxazol-4-yl)benzenesulfonamide Propanamide, N-[[4-(5-methyl-3-phenyl-4-isoxazolyl)phenyl]sulfonyl]- N-[[4-[5-methyl-3-phenylisoxazol-4-yl]phenyl]sulfonyl]acetamide Dynastat |
Description | Parecoxib is a potent and selective COX-2 inhibitor.IC50 value:Target: COX-2in vitro: The prodrug Parecoxib as well as its active metabolite val have a specific affinity to the cannabinoid (CB) receptor measured in CB1-expressing HEK 293 cells and rat brain tissue [1].in vivo: Adult male Sprague-Dawley rats were administered parecoxib (10 or 30 mg kg(-1), IP) or isotonic saline twice a day starting 24 h after middle cerebral artery occlusion (MCAO) for three consecutive days [2]. The selective COX-2 inhibitor parecoxib was delivered 20 min before or 20 min after the incision by intraperitoneal injection. Pretreatment with parecoxib markedly attenuated the pain hypersensitivity induced by incision [3]. |
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Related Catalog | |
Target |
COX-2 |
References |
Density | 1.3±0.1 g/cm3 |
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Melting Point | 148.9-151° |
Molecular Formula | C19H18N2O4S |
Molecular Weight | 370.422 |
Exact Mass | 370.098724 |
PSA | 101.14000 |
LogP | 1.72 |
Index of Refraction | 1.580 |
Symbol |
GHS08 |
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Signal Word | Warning |
Hazard Statements | H361d-H373 |
Precautionary Statements | P281 |
Hazard Codes | Xn,N |
Risk Phrases | 63-48/22-51/53 |
Safety Phrases | 36/37-61 |
RIDADR | NONH for all modes of transport |
RTECS | TX1478700 |
~82% 198470-84-7 |
Literature: Talley, John J.; Bertenshaw, Stephen R.; Brown, David L.; Carter, Jeffery S.; Graneto, Matthew J.; Kellogg, Michael S.; Koboldt, Carol M.; Yuan, Jinhua; Zhang, Yan Y.; Seibert, Karen Journal of Medicinal Chemistry, 2000 , vol. 43, # 9 p. 1661 - 1663 |
~75% 198470-84-7 |
Literature: Letendre, Leo J.; Kunda, Sastry A.; Gallagher, Donald J.; Seaney, Lisa M.; McLaughlin, Kathleen Patent: US2003/105334 A1, 2003 ; |
Precursor 2 | |
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DownStream 0 |