Sethi M L
J Nat Prod. 1979 Mar-Apr;42(2):187-96.
Benzophenanthridine alkaloids, fagaronine 4, O-methylfagaronine 5, nitidine 1, allonitidine 3 and methoxydihydronitidine 2 have been shown to posses inhibitory activity against reverse transcriptase of RNA tumor viruses. The enzyme inhibition (50%) by these alkaloids was found in the range of 6-60 microgram per milliliter of the reaction mixture when polynucleotide-oligodeoxynucleotide complexes were used as template primers. The results suggested that the benzophenanthridine alkaloids interacted with the template primers (particularly of the A:T base pairs) and not with the enzyme proteins. Kinetics reaction of the reverse transciptase inhibition showed that the alkaloids stopped the DNA polymerase synthesis instantly, probably by interacting with the template primer.
苯并菲啶生物碱,即白屈菜红碱4、O - 甲基白屈菜红碱5、两面针碱1、别两面针碱3和甲氧基二氢两面针碱2,已被证明对RNA肿瘤病毒的逆转录酶具有抑制活性。当使用多核苷酸 - 寡聚脱氧核苷酸复合物作为模板引物时,发现这些生物碱对酶的抑制率(50%)在反应混合物每毫升6 - 60微克的范围内。结果表明,苯并菲啶生物碱与模板引物(特别是A:T碱基对)相互作用,而不是与酶蛋白相互作用。逆转录酶抑制的动力学反应表明,生物碱可能通过与模板引物相互作用,立即停止DNA聚合酶的合成。