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Anti-HIV-1 activities of constituents from the rhizomes of Boesenbergia thorelii
A new lignan, thoreliin A (1), and a new bisnorlignan, thoreliin B (2), were isolated from a MeOH extract of the rhizomes of Boesenbergia thorelii. In addition, the known bisnorlignans 3 and 4, neolignan 5, phenylpropanoids 6–15, as well as benzenoids 18–21 were also obtained from the same source. T...
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Published in: | Fitoterapia 2019-11, Vol.139, p.104388, Article 104388 |
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creator | Thongphichai, Wisuwat Tuchinda, Patoomratana Pohmakotr, Manat Reutrakul, Vichai Akkarawongsapat, Radeekorn Napaswad, Chanita Limthongkul, Jitra Jenjittikul, Thaya Saithong, Saowanit |
description | A new lignan, thoreliin A (1), and a new bisnorlignan, thoreliin B (2), were isolated from a MeOH extract of the rhizomes of Boesenbergia thorelii. In addition, the known bisnorlignans 3 and 4, neolignan 5, phenylpropanoids 6–15, as well as benzenoids 18–21 were also obtained from the same source. The structures were elucidated based on their spectroscopic data. By single crystal X-ray analysis, the relative stereochemistry of 1 was confirmed. All isolated compounds were evaluated for anti-HIV-1 activities. Among them, thoreliin A (1) exhibited anti-HIV-1 activities on both HIV-1 reverse transcriptase (41.43% inhibition at 200 μg/mL) and syncytium reduction assays (EC50 20.6 μM, SI 3.7), while compounds 3–6, 9 and 11–21 showed anti-HIV-1 activity only in the anti-syncytium assay (EC50 6.6–454.1 μM, SI >1.32–7.75).
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doi_str_mv | 10.1016/j.fitote.2019.104388 |
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[Display omitted]</description><subject>Anti-HIV-1 activities</subject><subject>Antiviral activity</subject><subject>Aquatic plants</subject><subject>Benzenoids</subject><subject>Bisnorlignans</subject><subject>Boesenbergia</subject><subject>Boesenbergia thorelii</subject><subject>Crystal structure</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Lignan</subject><subject>Neolignans</subject><subject>Phenylpropanoids</subject><subject>Rhizomes</subject><subject>RNA-directed DNA polymerase</subject><subject>Single crystals</subject><subject>Stereochemistry</subject><subject>X ray analysis</subject><issn>0367-326X</issn><issn>1873-6971</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kE9LAzEQxYMoWKvfwMOC59RMkv13EWpRWyjooYi3kGYnNku7qUla0E_vlvXsaWDmvTe8HyG3wCbAoLhvJ9Yln3DCGdT9SoqqOiMjqEpBi7qEczJioiip4MXHJbmKsWUMciFhRN6mXXJ0vninkGmT3NElhzHzNjO-i8mlA3YpZjb4XZY2mIWN-_G7QfHoMWK3xvDpdH_0AbfOXZMLq7cRb_7mmKyen1azOV2-vixm0yU1omaJipKD1LowyAre5IYBlNoYrCspDVrNEbgWQtYNl9pUuNYm52itleum0SjG5G6I3Qf_dcCYVOsPoes_Ki54KaCCvO5VclCZ4GMMaNU-uJ0O3wqYOqFTrRrQqRM6NaDrbQ-DDfsCR4dBReOwM9i4gCapxrv_A34Bj0t6sw</recordid><startdate>201911</startdate><enddate>201911</enddate><creator>Thongphichai, Wisuwat</creator><creator>Tuchinda, Patoomratana</creator><creator>Pohmakotr, Manat</creator><creator>Reutrakul, Vichai</creator><creator>Akkarawongsapat, Radeekorn</creator><creator>Napaswad, Chanita</creator><creator>Limthongkul, Jitra</creator><creator>Jenjittikul, Thaya</creator><creator>Saithong, Saowanit</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>201911</creationdate><title>Anti-HIV-1 activities of constituents from the rhizomes of Boesenbergia thorelii</title><author>Thongphichai, Wisuwat ; 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In addition, the known bisnorlignans 3 and 4, neolignan 5, phenylpropanoids 6–15, as well as benzenoids 18–21 were also obtained from the same source. The structures were elucidated based on their spectroscopic data. By single crystal X-ray analysis, the relative stereochemistry of 1 was confirmed. All isolated compounds were evaluated for anti-HIV-1 activities. Among them, thoreliin A (1) exhibited anti-HIV-1 activities on both HIV-1 reverse transcriptase (41.43% inhibition at 200 μg/mL) and syncytium reduction assays (EC50 20.6 μM, SI 3.7), while compounds 3–6, 9 and 11–21 showed anti-HIV-1 activity only in the anti-syncytium assay (EC50 6.6–454.1 μM, SI >1.32–7.75).
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subjects | Anti-HIV-1 activities Antiviral activity Aquatic plants Benzenoids Bisnorlignans Boesenbergia Boesenbergia thorelii Crystal structure HIV Human immunodeficiency virus Lignan Neolignans Phenylpropanoids Rhizomes RNA-directed DNA polymerase Single crystals Stereochemistry X ray analysis |
title | Anti-HIV-1 activities of constituents from the rhizomes of Boesenbergia thorelii |
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