| 摘要 |
<p>A composition adapted to be topically applied to a mammal for treating mammalian peptic ulcer disease containing an effective amount of a prostaglandin analog in a pharmacuetical carrier suitable for administration to the skin of the mammal to be treated, said prostaglandin analog having a structure that corresponds to the formula: <CHEM> wherein: R has the formula -CH2- Y - (CH2)2-Z; -Y- is selected from the group consisting of -(CH2)-3 , cis -HC=CHCH2-, and cis,cis -HC=C=CH-; -Z is selected from the group consisting of -CH2 OH, and -CO2X, wherein X is hydrogen, a pharmacologically acceptable cation or C1-C6 alkyl; R<1> is n-butyl or phenoxy; R<2> is selected from the group consisting of hydrogen, methyl and hydroxyl; R<3> is selected from the group consisting of hydrogen, methyl and hydroxyl, with the proviso that R<2> and R<3> cannot both be hydrogen or both be hydroxyl; and R<4> and R<5> are the same or different and are selected from the group consisting of hydrogen and hydroxyl, but are not both hydroxyl. </p> |
