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穿心莲(Burm. F)Wall ex Nees:抗病毒特性。

Andrographis paniculata (Burm. F) Wall ex Nees: Antiviral properties.

机构信息

Department of Stem Cell and Regenerative Medicine, Centre For Interdisciplinary Research, DY Patil Education Society (Deemed to be University) Kolhapur, Kasaba Bawada, Maharashtra, 416006, India.

出版信息

Phytother Res. 2021 Oct;35(10):5365-5373. doi: 10.1002/ptr.7145. Epub 2021 Apr 30.

Abstract

Andrographis paniculata is home to a rich variety of molecules especially andrographolide and its derivatives. Clinical properties of the andrographolide are multifarious and include: analgesic, antipyretic, antiretroviral, antiproliferative, antimalarial, antithrombotic, antihyperglycemic, antiurolethial, antilesihmaniasis, hepatoprotective, immune-modulatory, protective against alcohol induced toxicity and cardioproetcive activity and anticancer activity. Andrographolide, neoandrographolide, dehydroandrographolide and several natural and synthetic derivatives of it: 14-deoxy-11,12-didehydroandrographolide and 14-deoxyandrographolide, dehydroandrographolide succinic acid monoester (DAMS), 14-ά-lipoyl andrographolide (AL-1), 14-acetyl-3,9-isopropyl-ideneandrographolide, 14-acetylandrographolide, 3,14,19-triacetylandrographolide, and 3,9-isopropyl-idene andrographolide, are shown to possess significant antiviral activity against HIV, influenza A, HBV, HCV, HPP and HSV. Studies on SARS CoV 2 is restricted to in silico molecular docking studies on viral targets and selected host target proteins. The main targets of andrographolide and its derivatives are fusion and adsorption of virus to the host cell, binding to viral receptor and co-receptor, enzymes involved in DNA/RNA/Genome replication by the virus, translation, post-translation and reverse transcription. Andrographolide as a drug is yet to reach its full therapeutic potential since this molecule shows low bioavailability. Andrographolide therapy is in need of an appropriate delivery system that may increase its bioavailability. Further high-quality studies are needed to firmly establish the clinical efficacy of the plant.

摘要

穿心莲含有丰富的化合物,特别是穿心莲内酯及其衍生物。穿心莲内酯具有多种临床特性,包括:镇痛、解热、抗逆转录病毒、抗增殖、抗疟、抗血栓形成、降血糖、抗尿石形成、抗丝虫病、保肝、免疫调节、对抗酒精毒性、心脏保护和抗癌活性。穿心莲内酯、新穿心莲内酯、去氢穿心莲内酯和几种其天然和合成衍生物:14-脱氧-11,12-去氢穿心莲内酯和 14-脱氧穿心莲内酯、去氢穿心莲内酯琥珀酸单酯(DAMS)、14-α-硫辛酸穿心莲内酯(AL-1)、14-乙酰基-3,9-异丙叉基穿心莲内酯、14-乙酰基穿心莲内酯、3,14,19-三乙酰基穿心莲内酯和 3,9-异丙叉基穿心莲内酯,均显示出对 HIV、流感 A、HBV、HCV、HHV-6 和 HSV 具有显著的抗病毒活性。对 SARS-CoV-2 的研究仅限于对病毒靶标和选定的宿主靶蛋白的计算机分子对接研究。穿心莲内酯及其衍生物的主要靶点是病毒与宿主细胞的融合和吸附、与病毒受体和辅助受体的结合、病毒参与 DNA/RNA/基因组复制的酶、翻译、翻译后和逆转录。穿心莲内酯作为一种药物尚未充分发挥其治疗潜力,因为这种分子的生物利用度较低。穿心莲内酯治疗需要适当的给药系统,以提高其生物利用度。需要进一步进行高质量的研究,以确定该植物的临床疗效。

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