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<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front cover</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md90022f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>569</fpage>
<lpage>570</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md90022f">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Contents list</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md90023d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>571</fpage>
<lpage>578</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md90023d">Abstract</self-uri>
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<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Water-soluble bis(1,10-phenanthroline) octanedioate Cu&lt;sup&gt;2+&lt;/sup&gt; and Mn&lt;sup&gt;2+&lt;/sup&gt; complexes with unprecedented nano and picomolar &lt;i&gt;in vitro&lt;/i&gt; cytotoxicity: promising leads for chemotherapeutic drug development</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c0md00266f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kellett</surname>
<given-names>Andrew</given-names></name>
<name><surname>O'Connor</surname>
<given-names>Mark</given-names></name>
<name><surname>McCann</surname>
<given-names>Malachy</given-names></name>
<name><surname>Howe</surname>
<given-names>Orla</given-names></name>
<name><surname>Casey</surname>
<given-names>Alan</given-names></name>
<name><surname>McCarron</surname>
<given-names>Pauraic</given-names></name>
<name><surname>Kavanagh</surname>
<given-names>Kevin</given-names></name>
<name><surname>McNamara</surname>
<given-names>Mary</given-names></name>
<name><surname>Kennedy</surname>
<given-names>Sean</given-names></name>
<name><surname>May</surname>
<given-names>Donald D.</given-names></name>
<name><surname>Skell</surname>
<given-names>Philip S.</given-names></name>
<name><surname>O'Shea</surname>
<given-names>Denis</given-names></name>
<name><surname>Devereux</surname>
<given-names>Michael</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>579</fpage>
<lpage>584</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c0md00266f">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and biological evaluation of novel 1-aryl, 5-(phenoxy-substituted)aryl-1,4-pentadien-3-one derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00038a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yuan</surname>
<given-names>Kai</given-names></name>
<name><surname>Song</surname>
<given-names>Baoan</given-names></name>
<name><surname>Jin</surname>
<given-names>Linhong</given-names></name>
<name><surname>Xu</surname>
<given-names>Shuai</given-names></name>
<name><surname>Hu</surname>
<given-names>Deyu</given-names></name>
<name><surname>Xu</surname>
<given-names>Xiaoqing</given-names></name>
<name><surname>Yang</surname>
<given-names>Song</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>585</fpage>
<lpage>589</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00038a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/MD/c1md00038a">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Online parallel fragment screening and rapid hit exploration for nicotinic acetylcholine receptors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00031d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kloe</surname>
<given-names>Gerdien E. de</given-names></name>
<name><surname>Kool</surname>
<given-names>Jeroen</given-names></name>
<name><surname>Elk</surname>
<given-names>Rene van</given-names></name>
<name><surname>Muijlwijk-Koezen</surname>
<given-names>Jacqueline E. van</given-names></name>
<name><surname>Smit</surname>
<given-names>August B.</given-names></name>
<name><surname>Lingeman</surname>
<given-names>Henk</given-names></name>
<name><surname>Irth</surname>
<given-names>Hubertus</given-names></name>
<name><surname>Niessen</surname>
<given-names>Wilfried M. A.</given-names></name>
<name><surname>Esch</surname>
<given-names>Iwan J. P. de</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>590</fpage>
<lpage>595</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00031d">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenyldiazenyl benzothiazole derivatives as probes for &lt;i&gt;in vivo&lt;/i&gt; imaging of neurofibrillary tangles in Alzheimer's disease brains</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00034a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Matsumura</surname>
<given-names>Kenji</given-names></name>
<name><surname>Ono</surname>
<given-names>Masahiro</given-names></name>
<name><surname>Hayashi</surname>
<given-names>Shun</given-names></name>
<name><surname>Kimura</surname>
<given-names>Hiroyuki</given-names></name>
<name><surname>Okamoto</surname>
<given-names>Yoko</given-names></name>
<name><surname>Ihara</surname>
<given-names>Masafumi</given-names></name>
<name><surname>Takahashi</surname>
<given-names>Ryosuke</given-names></name>
<name><surname>Mori</surname>
<given-names>Hiroshi</given-names></name>
<name><surname>Saji</surname>
<given-names>Hideo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>596</fpage>
<lpage>600</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00034a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/MD/c1md00034a">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Identification of target family directed bioisosteric replacements</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00066g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wassermann</surname>
<given-names>Anne Mai</given-names></name>
<name><surname>Bajorath</surname>
<given-names>Jürgen</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>601</fpage>
<lpage>606</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00066g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/MD/c1md00066g">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quantification of the orientations of pyrrolidine-based oxypeptide nucleic acid–DNA hybrid duplexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c0md00223b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kitamatsu</surname>
<given-names>Mizuki</given-names></name>
<name><surname>Sisido</surname>
<given-names>Masahiko</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>607</fpage>
<lpage>610</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c0md00223b">Abstract</self-uri>
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<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;N&lt;/i&gt;1-Benzyl substituted cambinol analogues as isozyme selective inhibitors of the sirtuin family of protein deacetylases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00023c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Medda</surname>
<given-names>Federico</given-names></name>
<name><surname>Joseph</surname>
<given-names>Thomas L.</given-names></name>
<name><surname>Pirrie</surname>
<given-names>Lisa</given-names></name>
<name><surname>Higgins</surname>
<given-names>Maureen</given-names></name>
<name><surname>Slawin</surname>
<given-names>Alexandra M. Z.</given-names></name>
<name><surname>Lain</surname>
<given-names>Sonia</given-names></name>
<name><surname>Verma</surname>
<given-names>Chandra</given-names></name>
<name><surname>Westwood</surname>
<given-names>Nicholas J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>611</fpage>
<lpage>615</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00023c">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Temocene: the porphycene analogue of temoporfin (Foscan®)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00065a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>García-Díaz</surname>
<given-names>María</given-names></name>
<name><surname>Sánchez-García</surname>
<given-names>David</given-names></name>
<name><surname>Soriano</surname>
<given-names>Jorge</given-names></name>
<name><surname>Sagristà</surname>
<given-names>M. Lluïsa</given-names></name>
<name><surname>Mora</surname>
<given-names>Margarita</given-names></name>
<name><surname>Villanueva</surname>
<given-names>Ángeles</given-names></name>
<name><surname>Stockert</surname>
<given-names>Juan C.</given-names></name>
<name><surname>Cañete</surname>
<given-names>Magdalena</given-names></name>
<name><surname>Nonell</surname>
<given-names>Santi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>616</fpage>
<lpage>619</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00065a">Abstract</self-uri>
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<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>RCAI-39, 41, 53, 100, 127 and 128, the analogues of KRN7000, activate mouse natural killer T cells to produce Th2-biased cytokines by their administration as liposomal particles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00067e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tashiro</surname>
<given-names>Takuya</given-names></name>
<name><surname>Ishii</surname>
<given-names>Yasuyuki</given-names></name>
<name><surname>Shigeura</surname>
<given-names>Tomokuni</given-names></name>
<name><surname>Nakagawa</surname>
<given-names>Ryusuke</given-names></name>
<name><surname>Watarai</surname>
<given-names>Hiroshi</given-names></name>
<name><surname>Taniguchi</surname>
<given-names>Masaru</given-names></name>
<name><surname>Mori</surname>
<given-names>Kenji</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>620</fpage>
<lpage>625</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00067e">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Antimycobacterial activity of spirooxindolo-pyrrolidine, pyrrolizine and pyrrolothiazole hybrids obtained by a three-component regio- and stereoselective 1,3-dipolar cycloaddition</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c0md00239a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rajesh</surname>
<given-names>Stephen Michael</given-names></name>
<name><surname>Perumal</surname>
<given-names>Subbu</given-names></name>
<name><surname>Menéndez</surname>
<given-names>J. Carlos</given-names></name>
<name><surname>Yogeeswari</surname>
<given-names>Perumal</given-names></name>
<name><surname>Sriram</surname>
<given-names>Dharmarajan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>626</fpage>
<lpage>630</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c0md00239a">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Binding of 9-&lt;i&gt;O&lt;/i&gt;-(ω-amino) alkyl ether analogues of the plant alkaloid berberine to poly(A): insights into self-structure induction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c0md00209g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Islam</surname>
<given-names>Md. Maidul</given-names></name>
<name><surname>Basu</surname>
<given-names>Anirban</given-names></name>
<name><surname>Kumar</surname>
<given-names>Gopinatha Suresh</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>631</fpage>
<lpage>637</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c0md00209g">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Triazole-substituted &lt;i&gt;N&lt;/i&gt;-hydroxyindol-2-carboxylates as inhibitors of isoform 5 of human lactate dehydrogenase (&lt;i&gt;h&lt;/i&gt;LDH5)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00071c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Granchi</surname>
<given-names>Carlotta</given-names></name>
<name><surname>Roy</surname>
<given-names>Sarabindu</given-names></name>
<name><surname>Fiandra</surname>
<given-names>Claudia Del</given-names></name>
<name><surname>Tuccinardi</surname>
<given-names>Tiziano</given-names></name>
<name><surname>Lanza</surname>
<given-names>Mario</given-names></name>
<name><surname>Betti</surname>
<given-names>Laura</given-names></name>
<name><surname>Giannaccini</surname>
<given-names>Gino</given-names></name>
<name><surname>Lucacchini</surname>
<given-names>Antonio</given-names></name>
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<given-names>Adriano</given-names></name>
<name><surname>Macchia</surname>
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<volume>2</volume>
<issue>7</issue>
<fpage>638</fpage>
<lpage>643</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00071c">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structure–activity relationships of gramicidin S analogs containing (β-3-pyridyl)-α,β-dehydroalanine residues on membrane permeability</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00081k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yamada</surname>
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<given-names>Shun-suke</given-names></name>
<name><surname>Komagoe</surname>
<given-names>Keiko</given-names></name>
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<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>644</fpage>
<lpage>649</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00081k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/MD/c1md00081k">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carbocyclic 5′-nor “reverse” fleximers. Design, synthesis, and preliminary biological activity</article-title>
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<article-id pub-id-type="doi">10.1039/c1md00094b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zimmermann</surname>
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<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>650</fpage>
<lpage>654</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00094b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/MD/c1md00094b">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
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<title-group>
<article-title>Discovery of novel selective Sigma-1 ligands as cognitive enhancers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00010a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Valade</surname>
<given-names>Anne</given-names></name>
<name><surname>Cross</surname>
<given-names>Sophie Binet</given-names></name>
<name><surname>Brown</surname>
<given-names>Claire</given-names></name>
<name><surname>Detrait</surname>
<given-names>Eric</given-names></name>
<name><surname>Ene</surname>
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<name><surname>Gillard</surname>
<given-names>Michel</given-names></name>
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<given-names>Michel</given-names></name>
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<name><surname>Maguire</surname>
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<name><surname>Namdev</surname>
<given-names>Nivedita</given-names></name>
<name><surname>Provins</surname>
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<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>655</fpage>
<lpage>660</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00010a">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<title-group>
<article-title>Second generation analogues of RKA182: synthetic tetraoxanes with outstanding &lt;i&gt;in vitro&lt;/i&gt; and &lt;i&gt;in vivo&lt;/i&gt; antimalarial activities</article-title>
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<article-id pub-id-type="doi">10.1039/c1md00102g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marti</surname>
<given-names>Francesc</given-names></name>
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<name><surname>Amewu</surname>
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<name><surname>Burrell-Saward</surname>
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<volume>2</volume>
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<fpage>661</fpage>
<lpage>665</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00102g">Abstract</self-uri>
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<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
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<title-group>
<article-title>Anti-colorectal cancer activity of an organometallic osmium arene azopyridine complex</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00075f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shnyder</surname>
<given-names>Steve D.</given-names></name>
<name><surname>Fu</surname>
<given-names>Ying</given-names></name>
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<given-names>Abraha</given-names></name>
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<given-names>Sabine H. van</given-names></name>
<name><surname>Cooper</surname>
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<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>666</fpage>
<lpage>668</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00075f">Abstract</self-uri>
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<article>
<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
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<title-group>
<article-title>Intramolecular hydrogen bonding to improve membrane permeability and absorption in beyond rule of five chemical space</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md00093d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alex</surname>
<given-names></given-names></name>
<name><surname>Millan</surname>
<given-names>David S.</given-names></name>
<name><surname>Perez</surname>
<given-names>Manuel</given-names></name>
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<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>669</fpage>
<lpage>674</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md00093d">Abstract</self-uri>
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<front>
<journal-meta>
<journal-title>MedChemComm</journal-title>
<issn>2040-2503</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Back cover</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1md90024b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>675</fpage>
<lpage>676</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1md90024b">Abstract</self-uri>
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