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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Veröffentlicht in:Asian Pacific journal of tropical biomedicine 2013-04, Vol.3 (4), p.284-290
Hauptverfasser: Kunsorn, Paween, Ruangrungsi, Nijsiri, Lipipun, Vimolmas, Khanboon, Ariya, Rungsihirunrat, Kanchana
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container_issue 4
container_start_page 284
container_title Asian Pacific journal of tropical biomedicine
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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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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 ; 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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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