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一种潜在抗病毒药物对器官培养中鼻病毒复制的抑制作用。

Inhibition of rhinovirus replication in in organ culture by a potential antiviral drug.

作者信息

DeLong D C, Reed S E

出版信息

J Infect Dis. 1980 Jan;141(1):87-91. doi: 10.1093/infdis/141.1.87.

Abstract

The compound 2-amino-1-(isopropyl sulfonyl)-6-benzimidazole phenyl ketone oxime (LY122771-72) at a concentration of 0.2 microgram/ml completely inhibited rhinovirus replication in human embryonic nasal organ cultures, although in the absence of virus the compound did not inhibit ciliary activity when used at a concentration of 25 micrograms/ml. When added 26 hr after infection, the compound stopped rhinovirus production in organ cultures that had already started to release virus. Five rhinovirus types available for infection of volunteers and six recently obtained clinical isolates were shown to be more sensitive to LY122771-72 in tissue culture than the rhinovirus type 31 used in the organ culture experiments. These results suggest that this potential antiviral drgu should be evaluated in humans.

摘要

化合物2-氨基-1-(异丙基磺酰基)-6-苯并咪唑苯乙酮肟(LY122771-72)浓度为0.2微克/毫升时,可完全抑制人胚鼻器官培养物中的鼻病毒复制,不过在无病毒情况下,该化合物浓度为25微克/毫升时并不抑制纤毛活性。感染后26小时添加该化合物,可使已开始释放病毒的器官培养物中的鼻病毒产生停止。在组织培养中,可用于志愿者感染的5种鼻病毒类型以及最近获得的6种临床分离株对LY122771-72的敏感性高于器官培养实验中使用的鼻病毒31型。这些结果表明,这种潜在的抗病毒药物应在人体中进行评估。

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