Graham S L, Shepard K L, Anderson P S, Baldwin J J, Best D B, Christy M E, Freedman M B, Gautheron P, Habecker C N, Hoffman J M
Merck Sharp & Dohme Research Laboratories, West Point, Pennsylvania 19486.
J Med Chem. 1989 Dec;32(12):2548-54. doi: 10.1021/jm00132a009.
Derivatives of benzo[b]thiophene-2-sulfonamide were prepared to investigate their potential utility as topically active inhibitors of ocular carbonic anhydrase. Such an agent would be useful in the treatment of glaucoma. Among the compounds described are 6-hydroxybenzo[b]thiophene-2-sulfonamide (16) and its acetate ester (23), which are among the most potent ocular hypotensive agents in this class, as assessed in the alpha-chymotrypsinized rabbit. These compounds were selected for clinical evaluation.
制备苯并[b]噻吩-2-磺酰胺的衍生物,以研究它们作为眼部碳酸酐酶局部活性抑制剂的潜在效用。这样一种药物将有助于青光眼的治疗。在所描述的化合物中,6-羟基苯并[b]噻吩-2-磺酰胺(16)及其乙酸酯(23),在经α-胰凝乳蛋白酶处理的兔子身上评估时,是这类药物中最有效的眼部降压剂之一。这些化合物被选作临床评估。