The identities and anti-herpes simplex virus activity of Clinacanthus nutans and Clinacanthus siamensis
Objective:To distinguish the difference among the Clinacanthus nutans(Burm.f.)Lindau(C.nutans)and Clinacanthus siamensis Bremek(C.siamensis)by assessing pharmacognosy characteristics,molecular aspect and also to evaluate their anti-herpes simplex virus(HSV)type 1 and type 2 activities.Methods:Macros...
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creator | Kunsorn, Paween Ruangrungsi, Nijsiri Lipipun, Vimolmas Khanboon, Ariya Rungsihirunrat, Kanchana |
description | Objective:To distinguish the difference among the Clinacanthus nutans(Burm.f.)Lindau(C.nutans)and Clinacanthus siamensis Bremek(C.siamensis)by assessing pharmacognosy characteristics,molecular aspect and also to evaluate their anti-herpes simplex virus(HSV)type 1 and type 2 activities.Methods:Macroscopic and microscopic evaluation were performed according to WHO Geneva guideline.Stomatal number,stomatal index and palisade ratio of leaves were evaluated.Genomic DNA was extracted by modified CTAB method and ITS region was amplified using PGR and then sequenced.Dry leaves were subsequently extracted with n-hexane,dichloromethane and methanol and antiviral activity was performed using plaque reduction assay and the cytotoxicity of the extracts on Vero cells was determined by MTT assay.Results:Cross section of midrib and stem showed similar major components.Leaf measurement index of stomatal number,stomatal index and palisade ratio of C.nutans were 168.32±29.49,13.83±0.86 and 6.84±0.66,respectively,while C.siamensis were 161.60±18.04,11.93±0.81and 3.37±0.31,respectively.The PCR amplification of ITS region generated the PGR product approximately 700 bp in size.There were 34 polymorphisms within the ITS region which consisted of 11 Indels and 23 nucleotide substitutions.The IC50values of C.nutans extracted with n-hexane,dichloromethane and methanol against HSV-1 were(32.05±3.63)μg/mL,(44.50±2.66)μg/mL,(64.93±7.00)μg/mL,respectively where as those of C.siamensis were(60.00±11.61)μg/mL,(55.69+4.41)μg/mL,(37.39±5.85)μg/mL,respectively.Anti HSV-2 activity of n-hexane,dichloromethane and methanol C.nutans leaves extracts were(72.62±12.60)μg/mL,(65.19±21.45)μg/mL,(65.13±2.22)μg/mL,respectively where as those of C.siamensis were(46.52±4.08)μg/mL,(49.63±2.59)μg/mL,(72.64±6.52)μg/mL,respectively.Conclusions:The combination of macroscopic,microscopic and biomolecular method are able to authenticate these closely related plants and both of them have a potency to be an anti-HSV agent. |
doi_str_mv | 10.1016/S2221-1691(13)60064-7 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3634925</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>1003038096</cqvip_id><els_id>S2221169113600647</els_id><sourcerecordid>2400449553</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4437-c6945693bd7f7d5f84acc693ecee8bf77edfcf75e528818b4fe35273af69bdf3</originalsourceid><addsrcrecordid>eNqFUU1r3DAQNaWlCWl-Qoqhl-TgVt-yLy1l6RcEesjehSyP1lNseSPZS_Pvo-xuQnKKQGg0773RjF5RXFDymRKqvtwwxmhFVUMvKb9ShChR6TfFKZN1XTUZfJvjR8pJcZ7SP5KXIoxJ8b44YVwxUkt2WmzWPZTYQZhxRkilDV3eM1Y9xG2-Jxy3A_wvdxiXjLoZdzjflZMvVwMG6zK3z0BYZhsO6hf5hHaEkDB9KN55OyQ4P55nxfrnj_Xqd3X999ef1ffrygnBdeVUI6RqeNtprzvpa2FdznFwAHXrtYbOO68lSFbXtG6FBy6Z5tarpu08Pyu-Hspul3aEzuW5oh3MNuJo452ZLJqXSMDebKad4YqLhslc4PJYIE63C6TZjJgcDIMNMC3JMEGIEI2U_FUq5UJJrfWeKg9UF6eUIvinjigxD46avaPmwa6sM3tHjc66j8_HeVI9-pcJ3w4EyH-6Q4gmOYTgoMMIbjbdhK8-8enYWj-FzS2GzbPeCCe8Jo3i91rMvsc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1346577753</pqid></control><display><type>article</type><title>The identities and anti-herpes simplex virus activity of Clinacanthus nutans and Clinacanthus siamensis</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Kunsorn, Paween ; Ruangrungsi, Nijsiri ; Lipipun, Vimolmas ; Khanboon, Ariya ; Rungsihirunrat, Kanchana</creator><creatorcontrib>Kunsorn, Paween ; Ruangrungsi, Nijsiri ; Lipipun, Vimolmas ; Khanboon, Ariya ; Rungsihirunrat, Kanchana</creatorcontrib><description>Objective:To distinguish the difference among the Clinacanthus nutans(Burm.f.)Lindau(C.nutans)and Clinacanthus siamensis Bremek(C.siamensis)by assessing pharmacognosy characteristics,molecular aspect and also to evaluate their anti-herpes simplex virus(HSV)type 1 and type 2 activities.Methods:Macroscopic and microscopic evaluation were performed according to WHO Geneva guideline.Stomatal number,stomatal index and palisade ratio of leaves were evaluated.Genomic DNA was extracted by modified CTAB method and ITS region was amplified using PGR and then sequenced.Dry leaves were subsequently extracted with n-hexane,dichloromethane and methanol and antiviral activity was performed using plaque reduction assay and the cytotoxicity of the extracts on Vero cells was determined by MTT assay.Results:Cross section of midrib and stem showed similar major components.Leaf measurement index of stomatal number,stomatal index and palisade ratio of C.nutans were 168.32±29.49,13.83±0.86 and 6.84±0.66,respectively,while C.siamensis were 161.60±18.04,11.93±0.81and 3.37±0.31,respectively.The PCR amplification of ITS region generated the PGR product approximately 700 bp in size.There were 34 polymorphisms within the ITS region which consisted of 11 Indels and 23 nucleotide substitutions.The IC50values of C.nutans extracted with n-hexane,dichloromethane and methanol against HSV-1 were(32.05±3.63)μg/mL,(44.50±2.66)μg/mL,(64.93±7.00)μg/mL,respectively where as those of C.siamensis were(60.00±11.61)μg/mL,(55.69+4.41)μg/mL,(37.39±5.85)μg/mL,respectively.Anti HSV-2 activity of n-hexane,dichloromethane and methanol C.nutans leaves extracts were(72.62±12.60)μg/mL,(65.19±21.45)μg/mL,(65.13±2.22)μg/mL,respectively where as those of C.siamensis were(46.52±4.08)μg/mL,(49.63±2.59)μg/mL,(72.64±6.52)μg/mL,respectively.Conclusions:The combination of macroscopic,microscopic and biomolecular method are able to authenticate these closely related plants and both of them have a potency to be an anti-HSV agent.</description><identifier>ISSN: 2221-1691</identifier><identifier>EISSN: 2588-9222</identifier><identifier>DOI: 10.1016/S2221-1691(13)60064-7</identifier><identifier>PMID: 23620852</identifier><language>eng</language><publisher>China: Elsevier B.V</publisher><subject>Acanthaceae - chemistry ; Acanthaceae - genetics ; analysis ; Antiviral Agents - chemistry ; Antiviral Agents - pharmacology ; antiviral properties ; assay ; Basic Researches ; Biomolecular ; Biomolecular analysis ; cetyltrimethylammonium bromide ; Clinacanthus ; Clinacanthus nutans ; Clinacanthus siamensis ; cytotoxicity ; DNA ; Flowers - chemistry ; Flowers - cytology ; Flowers - genetics ; guidelines ; Herpes ; Herpes simplex virus ; Herpesvirus 1, Human - drug effects ; Herpesvirus 2, Human - drug effects ; hexane ; Humans ; inhibitory concentration 50 ; Internal ; Internal transcribed spacer ; methanol ; methylene chloride ; Microscopic ; Microscopic analysis ; nutans ; pharmacognosy ; Phenotype ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Plant Leaves - chemistry ; Plant Leaves - cytology ; Plant Leaves - genetics ; Plaque ; Plaque reduction assay ; polymerase chain reaction ; reduction ; siamensis ; simplex ; Simplexvirus - drug effects ; spacer ; transcribed ; Viral Plaque Assay ; virus ; Virus Replication - drug effects ; viruses</subject><ispartof>Asian Pacific journal of tropical biomedicine, 2013-04, Vol.3 (4), p.284-290</ispartof><rights>2013 Asian Pacific Tropical Biomedical Magazine</rights><rights>2013 by the Asian Pacific Journal of Tropical Biomedicine. All rights reserved. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4437-c6945693bd7f7d5f84acc693ecee8bf77edfcf75e528818b4fe35273af69bdf3</citedby><cites>FETCH-LOGICAL-c4437-c6945693bd7f7d5f84acc693ecee8bf77edfcf75e528818b4fe35273af69bdf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/71871X/71871X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634925/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634925/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23620852$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kunsorn, Paween</creatorcontrib><creatorcontrib>Ruangrungsi, Nijsiri</creatorcontrib><creatorcontrib>Lipipun, Vimolmas</creatorcontrib><creatorcontrib>Khanboon, Ariya</creatorcontrib><creatorcontrib>Rungsihirunrat, Kanchana</creatorcontrib><title>The identities and anti-herpes simplex virus activity of Clinacanthus nutans and Clinacanthus siamensis</title><title>Asian Pacific journal of tropical biomedicine</title><addtitle>Asian Pacific Journal of Tropical Biomedicine</addtitle><description>Objective:To distinguish the difference among the Clinacanthus nutans(Burm.f.)Lindau(C.nutans)and Clinacanthus siamensis Bremek(C.siamensis)by assessing pharmacognosy characteristics,molecular aspect and also to evaluate their anti-herpes simplex virus(HSV)type 1 and type 2 activities.Methods:Macroscopic and microscopic evaluation were performed according to WHO Geneva guideline.Stomatal number,stomatal index and palisade ratio of leaves were evaluated.Genomic DNA was extracted by modified CTAB method and ITS region was amplified using PGR and then sequenced.Dry leaves were subsequently extracted with n-hexane,dichloromethane and methanol and antiviral activity was performed using plaque reduction assay and the cytotoxicity of the extracts on Vero cells was determined by MTT assay.Results:Cross section of midrib and stem showed similar major components.Leaf measurement index of stomatal number,stomatal index and palisade ratio of C.nutans were 168.32±29.49,13.83±0.86 and 6.84±0.66,respectively,while C.siamensis were 161.60±18.04,11.93±0.81and 3.37±0.31,respectively.The PCR amplification of ITS region generated the PGR product approximately 700 bp in size.There were 34 polymorphisms within the ITS region which consisted of 11 Indels and 23 nucleotide substitutions.The IC50values of C.nutans extracted with n-hexane,dichloromethane and methanol against HSV-1 were(32.05±3.63)μg/mL,(44.50±2.66)μg/mL,(64.93±7.00)μg/mL,respectively where as those of C.siamensis were(60.00±11.61)μg/mL,(55.69+4.41)μg/mL,(37.39±5.85)μg/mL,respectively.Anti HSV-2 activity of n-hexane,dichloromethane and methanol C.nutans leaves extracts were(72.62±12.60)μg/mL,(65.19±21.45)μg/mL,(65.13±2.22)μg/mL,respectively where as those of C.siamensis were(46.52±4.08)μg/mL,(49.63±2.59)μg/mL,(72.64±6.52)μg/mL,respectively.Conclusions:The combination of macroscopic,microscopic and biomolecular method are able to authenticate these closely related plants and both of them have a potency to be an anti-HSV agent.</description><subject>Acanthaceae - chemistry</subject><subject>Acanthaceae - genetics</subject><subject>analysis</subject><subject>Antiviral Agents - chemistry</subject><subject>Antiviral Agents - pharmacology</subject><subject>antiviral properties</subject><subject>assay</subject><subject>Basic Researches</subject><subject>Biomolecular</subject><subject>Biomolecular analysis</subject><subject>cetyltrimethylammonium bromide</subject><subject>Clinacanthus</subject><subject>Clinacanthus nutans</subject><subject>Clinacanthus siamensis</subject><subject>cytotoxicity</subject><subject>DNA</subject><subject>Flowers - chemistry</subject><subject>Flowers - cytology</subject><subject>Flowers - genetics</subject><subject>guidelines</subject><subject>Herpes</subject><subject>Herpes simplex virus</subject><subject>Herpesvirus 1, Human - drug effects</subject><subject>Herpesvirus 2, Human - drug effects</subject><subject>hexane</subject><subject>Humans</subject><subject>inhibitory concentration 50</subject><subject>Internal</subject><subject>Internal transcribed spacer</subject><subject>methanol</subject><subject>methylene chloride</subject><subject>Microscopic</subject><subject>Microscopic analysis</subject><subject>nutans</subject><subject>pharmacognosy</subject><subject>Phenotype</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Leaves - chemistry</subject><subject>Plant Leaves - cytology</subject><subject>Plant Leaves - genetics</subject><subject>Plaque</subject><subject>Plaque reduction assay</subject><subject>polymerase chain reaction</subject><subject>reduction</subject><subject>siamensis</subject><subject>simplex</subject><subject>Simplexvirus - drug effects</subject><subject>spacer</subject><subject>transcribed</subject><subject>Viral Plaque Assay</subject><subject>virus</subject><subject>Virus Replication - drug effects</subject><subject>viruses</subject><issn>2221-1691</issn><issn>2588-9222</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1r3DAQNaWlCWl-Qoqhl-TgVt-yLy1l6RcEesjehSyP1lNseSPZS_Pvo-xuQnKKQGg0773RjF5RXFDymRKqvtwwxmhFVUMvKb9ShChR6TfFKZN1XTUZfJvjR8pJcZ7SP5KXIoxJ8b44YVwxUkt2WmzWPZTYQZhxRkilDV3eM1Y9xG2-Jxy3A_wvdxiXjLoZdzjflZMvVwMG6zK3z0BYZhsO6hf5hHaEkDB9KN55OyQ4P55nxfrnj_Xqd3X999ef1ffrygnBdeVUI6RqeNtprzvpa2FdznFwAHXrtYbOO68lSFbXtG6FBy6Z5tarpu08Pyu-Hspul3aEzuW5oh3MNuJo452ZLJqXSMDebKad4YqLhslc4PJYIE63C6TZjJgcDIMNMC3JMEGIEI2U_FUq5UJJrfWeKg9UF6eUIvinjigxD46avaPmwa6sM3tHjc66j8_HeVI9-pcJ3w4EyH-6Q4gmOYTgoMMIbjbdhK8-8enYWj-FzS2GzbPeCCe8Jo3i91rMvsc</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Kunsorn, Paween</creator><creator>Ruangrungsi, Nijsiri</creator><creator>Lipipun, Vimolmas</creator><creator>Khanboon, Ariya</creator><creator>Rungsihirunrat, Kanchana</creator><general>Elsevier B.V</general><general>Asian Pacific Tropical Medicine Press</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20130401</creationdate><title>The identities and anti-herpes simplex virus activity of Clinacanthus nutans and Clinacanthus siamensis</title><author>Kunsorn, Paween ; Ruangrungsi, Nijsiri ; Lipipun, Vimolmas ; Khanboon, Ariya ; Rungsihirunrat, Kanchana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4437-c6945693bd7f7d5f84acc693ecee8bf77edfcf75e528818b4fe35273af69bdf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Acanthaceae - chemistry</topic><topic>Acanthaceae - genetics</topic><topic>analysis</topic><topic>Antiviral Agents - chemistry</topic><topic>Antiviral Agents - pharmacology</topic><topic>antiviral properties</topic><topic>assay</topic><topic>Basic Researches</topic><topic>Biomolecular</topic><topic>Biomolecular analysis</topic><topic>cetyltrimethylammonium bromide</topic><topic>Clinacanthus</topic><topic>Clinacanthus nutans</topic><topic>Clinacanthus siamensis</topic><topic>cytotoxicity</topic><topic>DNA</topic><topic>Flowers - chemistry</topic><topic>Flowers - cytology</topic><topic>Flowers - genetics</topic><topic>guidelines</topic><topic>Herpes</topic><topic>Herpes simplex virus</topic><topic>Herpesvirus 1, Human - drug effects</topic><topic>Herpesvirus 2, Human - drug effects</topic><topic>hexane</topic><topic>Humans</topic><topic>inhibitory concentration 50</topic><topic>Internal</topic><topic>Internal transcribed spacer</topic><topic>methanol</topic><topic>methylene chloride</topic><topic>Microscopic</topic><topic>Microscopic analysis</topic><topic>nutans</topic><topic>pharmacognosy</topic><topic>Phenotype</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Leaves - chemistry</topic><topic>Plant Leaves - cytology</topic><topic>Plant Leaves - genetics</topic><topic>Plaque</topic><topic>Plaque reduction assay</topic><topic>polymerase chain reaction</topic><topic>reduction</topic><topic>siamensis</topic><topic>simplex</topic><topic>Simplexvirus - drug effects</topic><topic>spacer</topic><topic>transcribed</topic><topic>Viral Plaque Assay</topic><topic>virus</topic><topic>Virus Replication - drug effects</topic><topic>viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kunsorn, Paween</creatorcontrib><creatorcontrib>Ruangrungsi, Nijsiri</creatorcontrib><creatorcontrib>Lipipun, Vimolmas</creatorcontrib><creatorcontrib>Khanboon, Ariya</creatorcontrib><creatorcontrib>Rungsihirunrat, Kanchana</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Asian Pacific journal of tropical biomedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kunsorn, Paween</au><au>Ruangrungsi, Nijsiri</au><au>Lipipun, Vimolmas</au><au>Khanboon, Ariya</au><au>Rungsihirunrat, Kanchana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The identities and anti-herpes simplex virus activity of Clinacanthus nutans and Clinacanthus siamensis</atitle><jtitle>Asian Pacific journal of tropical biomedicine</jtitle><addtitle>Asian Pacific Journal of Tropical Biomedicine</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>3</volume><issue>4</issue><spage>284</spage><epage>290</epage><pages>284-290</pages><issn>2221-1691</issn><eissn>2588-9222</eissn><abstract>Objective:To distinguish the difference among the Clinacanthus nutans(Burm.f.)Lindau(C.nutans)and Clinacanthus siamensis Bremek(C.siamensis)by assessing pharmacognosy characteristics,molecular aspect and also to evaluate their anti-herpes simplex virus(HSV)type 1 and type 2 activities.Methods:Macroscopic and microscopic evaluation were performed according to WHO Geneva guideline.Stomatal number,stomatal index and palisade ratio of leaves were evaluated.Genomic DNA was extracted by modified CTAB method and ITS region was amplified using PGR and then sequenced.Dry leaves were subsequently extracted with n-hexane,dichloromethane and methanol and antiviral activity was performed using plaque reduction assay and the cytotoxicity of the extracts on Vero cells was determined by MTT assay.Results:Cross section of midrib and stem showed similar major components.Leaf measurement index of stomatal number,stomatal index and palisade ratio of C.nutans were 168.32±29.49,13.83±0.86 and 6.84±0.66,respectively,while C.siamensis were 161.60±18.04,11.93±0.81and 3.37±0.31,respectively.The PCR amplification of ITS region generated the PGR product approximately 700 bp in size.There were 34 polymorphisms within the ITS region which consisted of 11 Indels and 23 nucleotide substitutions.The IC50values of C.nutans extracted with n-hexane,dichloromethane and methanol against HSV-1 were(32.05±3.63)μg/mL,(44.50±2.66)μg/mL,(64.93±7.00)μg/mL,respectively where as those of C.siamensis were(60.00±11.61)μg/mL,(55.69+4.41)μg/mL,(37.39±5.85)μg/mL,respectively.Anti HSV-2 activity of n-hexane,dichloromethane and methanol C.nutans leaves extracts were(72.62±12.60)μg/mL,(65.19±21.45)μg/mL,(65.13±2.22)μg/mL,respectively where as those of C.siamensis were(46.52±4.08)μg/mL,(49.63±2.59)μg/mL,(72.64±6.52)μg/mL,respectively.Conclusions:The combination of macroscopic,microscopic and biomolecular method are able to authenticate these closely related plants and both of them have a potency to be an anti-HSV agent.</abstract><cop>China</cop><pub>Elsevier B.V</pub><pmid>23620852</pmid><doi>10.1016/S2221-1691(13)60064-7</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acanthaceae - chemistry Acanthaceae - genetics analysis Antiviral Agents - chemistry Antiviral Agents - pharmacology antiviral properties assay Basic Researches Biomolecular Biomolecular analysis cetyltrimethylammonium bromide Clinacanthus Clinacanthus nutans Clinacanthus siamensis cytotoxicity DNA Flowers - chemistry Flowers - cytology Flowers - genetics guidelines Herpes Herpes simplex virus Herpesvirus 1, Human - drug effects Herpesvirus 2, Human - drug effects hexane Humans inhibitory concentration 50 Internal Internal transcribed spacer methanol methylene chloride Microscopic Microscopic analysis nutans pharmacognosy Phenotype Plant Extracts - chemistry Plant Extracts - pharmacology Plant Leaves - chemistry Plant Leaves - cytology Plant Leaves - genetics Plaque Plaque reduction assay polymerase chain reaction reduction siamensis simplex Simplexvirus - drug effects spacer transcribed Viral Plaque Assay virus Virus Replication - drug effects viruses |
title | The identities and anti-herpes simplex virus activity of Clinacanthus nutans and Clinacanthus siamensis |
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