Synthesis and antitrypanosomal activities of a series of 7-deaza-5'-noraristeromycin derivatives with variations in the cyclopentyl ring substituents.
1997 ◽
Vol 41
(8)
◽
pp. 1658-1661
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Keyword(s):
Previous work in our laboratories has suggested that (+)-5'-nor-7-deazaaristeromycin (compound 1) may represent a prototype structure for a series of compounds with significant antitrypanosomal activities. To test this possibility, a series of derivatives of compound 1 with changes in the cyclopentyl substituents (compounds 3 to 10) have been studied. Although some growth activity was obtained with the L-like compound 5, related compounds 3 and 7 had little or no activity below 100 microM. D-like compounds 4 and 6 showed some activity at or below 100 microM, but the most interesting finding was that both the D- and L-like compounds having a methyl substituent on the 4' position were most active.
1996 ◽
Vol 61
(s1)
◽
pp. 122-123
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1991 ◽
Vol 195
(1)
◽
pp. 239-249
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Keyword(s):
1972 ◽
Vol 23
(2)
◽
pp. 275-282
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1950 ◽
Vol 0
(0)
◽
pp. 2130-2134
◽
Keyword(s):
1974 ◽
pp. 1771
◽
Keyword(s):