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filingDate 1990-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d0bff2c24626f232f8e0b5a3cc9bf26
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publicationDate 1991-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H03130220-A
titleOfInvention Prodrug for carbonic anhydrase inhibitor
abstract NEW MATERIAL: This compound is shown by formula I to formula III [Z is a water-soluble carrier; A is a group capable of maintaining carbonic anhydrase inhibiting activity and forming a bond enzymatically cleavable bond with Z when added to (a) 2-benzothiazosulfonamide, (b) hydroxy methazolamide or (c) dichlorphenamide]. n EXAMPLE: 6-[β-(Glucopyranosyl)oxyethoxy-2-benzothiazolesulfonamide. n USE: A prodrug for carbonic anhydrase inhibitor(CAI) useful for locally treating glaucoma, increased water solubility of CAI without exerting bad influence on CAI activity. n PROCESS: Especially a water-soluble carrier containing the whole OHs protected except a reaction site with A is reacted with a CAI analog of the substance (a) to (c) under a proper reaction condition and the Z protecting group is removed to give compounds of formula I to formula III. n COPYRIGHT: (C)1991,JPO
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priorityDate 1989-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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