Design and Synthesis of Celecoxib and Rofecoxib Analogues as Selective Cyclooxygenase-2 (COX-2) Inhibitors: Replacement of Sulfonamide and Methylsulfonyl Pharmacophores by an Azido Bioisostere
β Scribed by Habeeb, Amgad G.; Praveen Rao, P. N.; Knaus, Edward E.
- Book ID
- 120182637
- Publisher
- American Chemical Society
- Year
- 2001
- Tongue
- English
- Weight
- 127 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-2623
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π SIMILAR VOLUMES
A group of rofecoxib analogs, having a sulfonylazide (SO 2 N 3 ) substituent in place of the methanesulfonyl (SO 2 CH 3 ) pharmacophore at the meta-position viz 3-( 4-methyl, 4-methoxy, or 4-ethoxyphenyl)-4-(3-sulf o n y l a z i d o p h e n y l ) -2 ( 5H)furanone (7 a -c) and p a r a-position v i z
## Abstract A group of 1,2βdiphenylβ3,5βdioxopyrazolidines possessing a methylsulfonyl (**11**) or sulfonamide (**15**) substituent at the __para__ position of the __N__^1^βphenyl ring, in conjunction with a hydrogen, methyl or fluoro subβstituent at the __para__ position of the __N__^2^βphenyl rin