Carbonic anhydrase inhibitors. Part 43. Schiff bases derived from aromatic sulfonamides: Towards more specific inhibitors for membrane-bound versus cytosolic isozymes

DOI: 10.1016/S0223-5234(97)81681-9

Source and publish data:

European Journal of Medicinal Chemistry p. 445 - 452 (1997)

Update date:2022-08-04

Topics:

Authors:

Supuran Supuran

Scozzafava

Popescu Popescu

Bobes-Tureac

Banciu Banciu

Creanga Creanga

Bobes-Tureac

Banciu Banciu

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Article abstract of DOI:10.1016/S0223-5234(97)81681-9

Schiff bases were prepared by reaction of sulfanilamide, homosulfanilamide and p-aminoethyl-benzenesulfonamide with substituted benzene- and heterocyclic aldehydes. The compounds were characterized by standard procedures and were assayed as inhibitors of

Full text of DOI:10.1016/S0223-5234(97)81681-9

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Product name:Benzenesulfonamide, 4-[[[(3-nitrophenyl)methylene]amino]methyl]-

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