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<title cf:type="text"><![CDATA[Chinese Herbal Medicines -->Short Communication]]></title>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Opening up a Way of Evaluating Evidence-based Medicine in Traditional Chinese Medicine]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM-1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[JIA Zhen-hua]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>JIA Zhen-hua</atom:name>
</atom:author>
<guid><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM-1]]></guid><cfi:id>9</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Pharmacopoeia of the People’s Republic of China (2010 Edition): A Milestone in Development of China’s Healthcare]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM-2]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[QIAN Zhong-zhi,DAN Yang,LIU Yan-ze and PENG Yong]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>QIAN Zhong-zhi,DAN Yang,LIU Yan-ze and PENG Yong</atom:name>
</atom:author>
<guid><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM-2]]></guid><cfi:id>8</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Yerba Mate or Paraguay Tea]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201403011]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate>2014/8/28 9:46:22</pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[Viviane Linck,Ivone Manzali de Sá and Elaine Elisabetsky]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Viviane Linck,Ivone Manzali de Sá and Elaine Elisabetsky</atom:name>
</atom:author>
<guid><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201403011]]></guid><cfi:id>7</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Chemical Constituents from Barks of Lannea coromandelica]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201401009]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Objective  To study the chemical constituents from the barks of Lannea coromandelica. Methods  The chemical constituents were isolated and purified by column chromatography on silica gel column. NMR spectra were used for structural identification. Results  Thirteen compounds were isolated and identified as quercetin (1), (2S,3S,4R,10E)-2-[(2′R)-2′-hydroxytetracosanoyl amino]-10-octadecene-1,3,4- triol (2), aralia cerebroside (3), 5,5′-dibuthoxy-2,2′-bifuran (4), β-sitosteryl- 3β-glucopyranoside-6′-O-palmitate (5), β-sitosterol palmitate (6), myricadiol (7), protocatechuic acid (8), p-hydroxybenzoic acidethyl ester (9), isovanillin (10), trans- cinnamic acid (11), palmitic acid (12), and stearic acid (13). Conclusion  Compounds 2?13 are isolated from this plant for the first time.]]></description>
<pubDate>2014/2/14 13:48:50</pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[Xiao-juan Yun,Huo-ming Shu,Guang-ying Chen,Ming-hui Ji and Jin-yue Ding]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Xiao-juan Yun,Huo-ming Shu,Guang-ying Chen,Ming-hui Ji and Jin-yue Ding</atom:name>
</atom:author>
<guid><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201401009]]></guid><cfi:id>6</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[A New Hasubanan Alkaloid from Stephania hernandifolia]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201401010]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Objective  To study the chemical constituents of Stephania hernandifolia. Methods  Various chromato- graphic techniques were used to isolate the constituents, and the structures were elucidated on the basis of HR-EI-MS, 1D-NMR and 2D-NMR spectral analyses. Results  A hasubanan alkaloid, hernsubanine D (1) was isolated from the whole plants of S. hernandifolia. The compound was screened for the cytotoxic activity against two human cancer cell lines in vitro. Conclusion  Compound 1 is a new compound without cytotoxicity against A549 and K562 cells.]]></description>
<pubDate>2014/2/14 13:48:50</pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[Lu-lu Deng,Li-jia Tang,Huan-yu Guan,Li He,Jian-xin Zhang,Jian-hua Liu,Xiao-jiang Hao and Yuan-hu Zhang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Lu-lu Deng,Li-jia Tang,Huan-yu Guan,Li He,Jian-xin Zhang,Jian-hua Liu,Xiao-jiang Hao and Yuan-hu Zhang</atom:name>
</atom:author>
<guid><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201401010]]></guid><cfi:id>5</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[A New Secoiridoid Glycoside from Swertia cincta]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201401011]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Objective  To study the chemical constituents of Swertia cincta. Methods  Preparative liquid chromatography was employed. The structures of the compounds were elucidated by spectroscopic analysis. Results  Three secoiridoid glycosides were isolated from S. cincta and identified as 8-methoxyl-eustomorusside (1), secoiridoids eustomorusside (2), and eustomoside (3). Conclusion  Compound 1 is a new secoiridoid glycoside. Compounds 2 and 3 are isolated from this plant for the first time.]]></description>
<pubDate>2014/2/14 13:48:50</pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[Fei-yan Huang,Jian-jun Wu and Gan-peng Li]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Fei-yan Huang,Jian-jun Wu and Gan-peng Li</atom:name>
</atom:author>
<guid><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201401011]]></guid><cfi:id>4</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Isolation and Identification of Bioactive Constituents from Stem Barks of Illicium difengpi]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201401012]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Objective  To isolate and identify bioactive constituents from the stem barks of Illicium difengpi. Methods  The chemical constituents were isolated and purified by repeated silica gel, Sephadex LH-20, recrystallization, and preparative HPLC techniques. The structures of the compounds were identified on the basis of spectral data including NMR, MS, and IR. Results  Two sesquiterpene lactones, majucin (1) and anisatin (2), two steroids, β-sitosterol (3) and daucosterol (4), three carboxylic acids, 2-ethyldecanoic acid (5), shikimic acid (6), and 3,4-dihydrobenzoic acid (7), and a flavonoid, quercetin (8), were successively isolated from the stem barks of I. difengpi. Conclusion  Apart from compound 3, other seven compounds are reported in this plant for the first time. The results suggested that the current studies on I. difengpi is still far from being well known and therefore more studies need to be done for better understanding of this plant.]]></description>
<pubDate>2014/2/14 13:48:50</pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[Yong-zhi He,Eric Kibagendi Osoro,Sivoko Imbenzi Palmer,Li-ning Wang and Naji Said Aboud]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Yong-zhi He,Eric Kibagendi Osoro,Sivoko Imbenzi Palmer,Li-ning Wang and Naji Said Aboud</atom:name>
</atom:author>
<guid><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201401012]]></guid><cfi:id>3</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Chemical Constituents from Mycelia and Spores of Fungus Cordyceps cicadae]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201702012]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Objective  To isolate and identify the chemical constituents from mycelia and spores of the fungus Cordyceps cicadae, respectively. Methods  The chemical constituents were isolated and purified by repeated silica gel, Sephadex LH-20, and reversed phase HPLC. The structures of these compounds were elucidated on the basis of extensive spectroscopic analysis, including 1D and 2D NMR. Results  Nine known sterols such as ergosterol (1), ergosterol peroxide (2), 9,11-dehydroergosterol peroxide (3), 3β,5α,9α- trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one (4), 3β,5α,9α,14α-tetrahydroxy-(22E, 24R)-ergosta-7,22-dien-6-one (5), 5α,6α-epoxy-(22E,24R)-ergosta-8(14),22-diene- 3β,7α-diol (6), 3β,5α,6β-(22E,24R)-ergosta-7,22-dien-3,5,6-triol (7), 3β,5α,6α-6- methoxyergosta-(22E,24R)-7,22-diene-3,5-diol (8), 4-hydroxy-17R-methylincisterol (9), together with a resorcinol derivative, 5-n-nonadecylresorcinol (10), a cyclo- desipeptide, beauvericin (11), and a nucleoside, N6-(2-hydroxyethyl)adenosine (12) were successively isolated from the cultivated C. cicadae mycelia and spores. Conclusion Compounds 3?10 are reported for the first time from the title sample, beauvericin exhibits significant cytotoxicity against human leukemia cell line and human lung cancer cell line.]]></description>
<pubDate>2017/5/2 17:04:14</pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[Jia-hui Wang1, 2,Zhong-liang Zhang3, 4,Yu-qin Wang3, 4,Min Yang2,Chun-hua Wang1,Xu-wen Li2 and Yue-wei Guo2]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Jia-hui Wang1, 2,Zhong-liang Zhang3, 4,Yu-qin Wang3, 4,Min Yang2,Chun-hua Wang1,Xu-wen Li2 and Yue-wei Guo2</atom:name>
</atom:author>
<guid><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201702012]]></guid><cfi:id>2</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Triterpenoids from Whole Plants of Phyllanthus urinaria]]></title>
<link><![CDATA[https://www.tiprpress.com/chmen/article/abstract/CHM201702013]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Objective  To study the chemical constituents of whole plant of Phyllanthus urinaria and their biological activity. Methods  The chemical constituents were isolated and purified by repeated column chromatography over silica gel, Rp-C18 (reverse phase), MCI, and Sephadex LH-20, as well as semi-preparative HPLC. NMR spectroscopic analyses were used for the structure identification. In this case, the inhibitory rate of NO production of the isolated triterpenoids was evaluated. Results  Seven triterpenoids, identified as 28-norlup-20(29)-ene-3,17β-diol (1), betulin (2), β-betulinic acid (3), 3-oxo- friedelan-28-oic acid (4), oleanolic acid (5), 3R-E-coumaroyltaraxerol (6), and 3R-Z- coumaroyltaraxerol (7), were isolated and identified from the whole plants of P. urinaria. Compounds 1?5 exerted inhibitory effects against NO production in LPS-induced RAW 264.7 mouse macrophages with the inhibitory rate of NO production ranging from 4.0% to 27.8% at the concentration of 25 μmol/L. Conclusion  To the best of our knowledge, this is the first report of compounds 1?4, 6, and 7 from the family Euphorbiaceae. Compounds 1?5 exhibited inhibitory effects against NO production in LPS-induced RAW 264.7 mouse macrophages.]]></description>
<pubDate>2017/5/2 17:04:14</pubDate>
<category><![CDATA[Short Communication]]></category>
<author><![CDATA[Ye Wu1, 2,Shuang-shuang Xie2,Zheng-xi Hu2,Zhao-di Wu2,Yi Guo2,Jin-wen Zhang1,Jian-ping Wang2,Yong-bo Xue2 and Yong-hui Zhang2]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Ye Wu1, 2,Shuang-shuang Xie2,Zheng-xi Hu2,Zhao-di Wu2,Yi Guo2,Jin-wen Zhang1,Jian-ping Wang2,Yong-bo Xue2 and Yong-hui Zhang2</atom:name>
</atom:author>
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