网址：//www.xcmww.com/md 清华大学，2018年10月18日12:53:43+0000 en美国 每小时 1个 https://wordpress.org/？V= 4.9 //www.xcmww.com/md/2018/10/18/2019-medchemcomm-emerging-researcher-steacheship-nominations-open/ //www.xcmww.com/md/2018/10/18/2019 Medchemcomm新兴研究者讲师提名公开/回复 清华大学，2018年10月18日11:09:14+0000 詹姆斯·安森 讲师职位 //www.xcmww.com/md/？P＝2940 2019年的Medchemcomm新兴研究者演讲现已开放提名。提名将于2018年11月22日结束。讲师的接受者将获得高达1000英镑的捐款，用于在2019年的一次会议上发言。资格：讲师资格对2009年或之后获得博士学位并拥有[…]学位的候选人开放。 <p>2019年的Medchemcomm<em>Emerging Investor讲师现在开始提名。<p><p><strong>提名将于2018年11月22日结束。<strong><p><p>The Recipient of the Teacheship will receive a contribution of up to£1000 to speaking at a conference in 2019.<p><p><strong>qualification<br/>.<strong>The Teacheship is open对2009年或以后获得博士学位并在其早期职业生涯中对药物化学做出重大贡献的候选人，新利手机客户端尤其是如果他们给药物发现带来了新的想法。<p><p><strong>How you can insignate<br/>.<strong>if you want to insignate someone please email us（medchemcomm-rsc@rsc.org）with the following details:<p><ul><li>their name.<li><li>their affiliation.<li><u>at least.<u>one paragraph explaining their accounts and why you t请注意，他们应该被考虑到</li><ul><p>additional supporting information，例如他们的简历，很有助于做出决定，但不是作出提名的强制要求。<p><p>self-nominations are accepted but<u>must<u>be supported by a letter of support from your departments head of departments or similar person at your institute.<p><p><strong>selection<br/>.<strong>all qualified nominations will be considered and a short list of candidat根据提名时提供的信息进行选择。编委会随后将投票选择接收者，获胜者将在2018年底宣布。<p>Previous Teacheship Winners include:<p><ul><li>dr.Gon_alo Bernardes（剑桥大学，英国）–2018<<li>Dr Laura H.海特曼（莱顿大学，荷兰）–2017<<li>Dr Alessio Ciulli（University of Dundee，英国）–2016-<li>Richard Payne教授（悉尼大学，澳大利亚）–2015</li><li>教授Christian Heinis（_cole polytechnique f_d_rale de lausanne，瑞士）–2013-<li>Patrick Gunning教授（多伦多大学，加拿大）–2012</li><ul><div class=“lightsocial_container”><a class=“lightsocial_a”href=“http://digg.com/submit”？url=http%3a%2f%2fwww.xcmww.com%2fmd%2f2018%2f10%2f18%2f2019 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social_img”src=“//www.xcmww.com/md/wp-content/plugins/light-social/google_buzz.png”alt=“google buzz（aka）。google reader）“title=”google buzz（aka.google reader）“/>.<a>.<div> //www.xcmww.com/md/2018/10/18/2019-medchemcomm-emerging-researcher-steacheship-nominations-open/feed/ 零 //www.xcmww.com/md/2018/09/07/medchemcomm-welcome-professor-jayanta-haldar-to-the-editional-board/ //www.xcmww.com/md/2018/09/07/medchemcomm欢迎Jayanta Haldar教授来到编辑委员会/回复 周五，2018年9月7日12:21:37+0000 Catherine Hodges-开发编辑 董事会新闻 //www.xcmww.com/md/？P＝2946 我们很高兴地欢迎贾瓦哈拉尔-尼赫鲁高级科学研究中心（JNCSR）的团队教授贾亚纳塔·霍尔达尔（Jayanta Haldar）。班加罗尔，印度。Jayanta在总统学院学习，加尔各答大学在进入印度科学院之前，新利手机客户端班加罗尔获得理学硕士学位。博士学位。2004年，他在……担任博士后职位。 <p><a href=“//www.xcmww.com/md/files/2018/09/jh photo.jpg”><img class=“wp-image-2947 AlignRight”src=“//www.xcmww.com/md/files/2018/09/jh-photo-265x300.jpg”alt=“”width=“201”height=“227”srcset=“//www.xcmww.com/md/files/2018/09/jh-photo-265x300.jpg 265W，//www.xcmww.com/md/files/2018/09/jh-photo.jpg 582w“尺寸=”（最大宽度：201px）100vw，201px“/></a><p><p>we are plexful to welcome to welcome to the team professor jayanta haldar of the jawaharlal nehru centre for advanced scientific research（jncasr），班加罗尔，印度。<p>Jayanta在总统学院学习，加尔各答大学在进入印度科学院之前，新利手机客户端班加罗尔获得理学硕士学位。博士学位。2004年，他在麻省理工学院担任博士后职位，美国亚历山大·克里巴诺夫。随后，Jayanta回到印度，在JNCSR担任助理教授职位，他现在的教职员工，他于2015年被任命为副教授。<p>Haldar教授的团队专门从事新型抗菌治疗的开发，涂层和表面，以及新型的药物纳米输送系统。为了了解更多关于他的研究，查看组网页<a href=“http://www.jncasr.ac.in/jayanta/index.html”，或阅读他的许多出版物：<p><p>.<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c8cc01926f“>通过调节膜活性肽组分两亲的分子设计来选择性地靶向细菌</a><strong><p><strong><em>chem。公社。.<em>.<strong>，2018年，<strong>54<strong>，49 43-49 46<a href=“http://xlink.rsc.org/？doi=10.1039/c8cc01926f“>doi:10.1039/c8cc01926f<a>><p>><p>><p>><strong>><a href=“http://xlink.rsc.org/？doi=10.1039/c7cc04206j“>L-赖氨酸基脂质联苯作为具有抗生物膜和抗炎特性的药剂，也抑制细胞内细菌</a><strong><p><strong><em>chem。公社。.<em>.<strong>，2017年，<strong>53<strong>，8427-8430，<a href=“http://xlink.rsc.org/？doi=10.1039/c7cc04206j“>doi:10.1039/c7cc04206j</a>><p>><p>><p>><strong>><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00585c“>a review on cell wall synthesis inhibitors with an emphasis on glycopenide anticists.<a><strong><p><strong><em>med.化学。公社。.<em>.<strong>，2017年，<strong>8<strong>，516-533，<a href=“http://xlink.rsc.org/？doi=10.1039/c6md00585c“>doi:10.1039/c6md00585c<a>><p>><p>><p>><strong>><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00589f“>芳基烷基赖氨酸：small molecular membrane active antiplasmodial agents</a><strong><p><strong><em>med.化学。公社。.<em>.<strong>，2017年，<strong>8<strong>，434-439页，<a href=“http://xlink.rsc.org/？doi=10.1039/c6md00589f“>doi:10.1039/c6md00589f</a><p><div class=“lightsocial_container”><a class=“lightsocial_a”href=“http://digg.com/submit”？url=http%3a%2f%2fwww.xcmww.com%2fmd%2f2018%2f09%2f07%2fmedchemcomm欢迎Jayanta Haldar教授来到编辑委员会%2f&title=Medchemcomm+Welcomes+Professor+Jayanta+Haldar+to+the+editional+board“><img class=“light social\u 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//www.xcmww.com/md/2018/09/07/medchemcomm-welcome-profer-jayanta-haldar-to-the-editional-board/feed/ 零 //www.xcmww.com/md/2018/05/14/editor-in-chief-gerhard-ecker/ //www.xcmww.com/md/2018/05/14/editor in chief gerhard ecker/回复 周一，2018年5月14日10:44:27+0000 Catherine Hodges-开发编辑 董事会新闻 //www.xcmww.com/md/？P＝2927 Medchemcomm非常高兴欢迎来到我们的新主编团队，格哈德·埃克教授。教授埃克目前是维也纳大学药物化学系药物信息学研究小组的负责人。新利手机客户端他的研究兴趣包括配体和结构药物设计，聚焦于跨膜转运蛋白和[…]的预测 <p><a href=“//www.xcmww.com/md/files/2018/05/ge photo.jpg”><img class=“AlignRight wp-image-2931”src=“//www.xcmww.com/md/files/2018/05/ge-photo-210x300.jpg”alt=“medchemcomm主编gerhard ecker”width=“148”height=“211”srcsset=“//www.xcmww.com/md/files/2018/05/ge-photo-210x300.jpg 210w，//www.xcmww.com/md/files/2018/05/ge-photo-768x1096.jpg 768W，//www.xcmww.com/md/files/2018/05/ge-photo-718x1024.jpg 718w“尺寸=”（最大宽度：148px）100vw，148px“/><a><p><p style=“text-align:justify”><em>medchemcomm<em>is very exceered to welcome to the team our new editor in chief，格哈德·埃克教授。教授埃克目前是维也纳大学药物化学系药物信息学研究小组的负责人。新利手机客户端他的研究兴趣包括配体和结构药物设计，重点研究跨膜转运蛋白和开关动力学预测，以及语义数据集成。<p><p style=“text-align:justify”>他在Fleischhacker教授和Noe教授的监督下完成了维也纳大学的博士学位，之后在Borstel担任Seydel教授的组的博士后职位，德国。<p><p style=“text-align:justify”>Gerhard曾担任欧洲药物化学联合会主席和奥地利药物学会副主席。<p><p><p><p>He has published over 100 full papers，新利手机客户端包括：<p><p><a href=“http://xlink.rsc.org/？doi=10.1039/c0cc03075a“><strong>探讨P-糖蛋白合成的立体选择性，对映体纯苯并吡喃[3,4-b][1,4]恶嗪组的生物活性和配体对接研究公社。<em>，2011，47岁，2586-2588<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00065g“>open-phacts calculational protocols for in-silico target validation of cellular-hypomic screens:knowing the knowns.<a>><br/><em>med.化学。公社。<em>，2016，7号，1237-1244<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00207b“>From linked open data to molecular interaction:studing selective trends for配体of the human serotonin and dopamine transporter.<a><strong><br/><em>med.化学。公社。<em>，2016，7号，1819-1831</p><p><p><p>for more information，访问他的实验室组网站url=http%3a%2f%2fwww.xcmww.com%2fmd%2f2018%2f05%2f14%2feditor in chief gerhard ecker%2f&title=introducing+new+medchemcomm+editor in chief%2c+教授+gerhard+ecker“><img class=“light social\u img”src=“//www.xcmww.com/md/wp-content/plugins/light-social/digg.png”alt=“digg this”title=“digg”/><<a class=“light social”>a/www.reddit.com/submit？url=http%3a%2f%2fwww.xcmww.com%2fmd%2f2018%2f05%2f14%2feditor in chief gerhard ecker%2f&title=introducing+new+medchemcomm+editor in chief%2c+教授+gerhard+ecker“><img class=“light social\u img”src=“//www.xcmww.com/md/wp-content/plugins/light-social/reddit.png”alt=“reddit this”title=“reddit”/><<a class=“light social\u a”href=“hTTP://www.stumbleupon.com/submit？提交？url=http%3a%2f%2fwww.xcmww.com%2fmd%2f2018%2f05%2f14%2feditor in chief gerhard ecker%2f&title=introducing+new+medchemcomm+editor in chief%2c+教授+gerhard+ecker“><img class=“light social”img“src=”//www.xcmww.com/md/wp-content/plugins/light-social/stumbleupon.png“alt=”stumble 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social_img”src=“//www.xcmww.com/md/wp-content/plugins/light-social/google_buzz.png”alt=“google buzz（aka）。google reader）“title=”google buzz（aka.google reader）“/>.<a>.<div> //www.xcmww.com/md/2018/05/14/editor-in-chief-gerhard-ecker/feed/ 零 //www.xcmww.com/md/2018/03/20/outstanding-reviewers-for-medchemcomm-in-2017/ //www.xcmww.com/md/2018/03/20/outstanding-reviewers-for-medchemcomm-in-2017/回复 星期二，2018年3月20日11:00:24+0000 艾米·库克 新闻 //www.xcmww.com/md/？P=2922 2017年Medchemcomm优秀审稿人，我们希望突出2017年Medchemcomm优秀审稿人。根据编辑组的选择，因为他们对杂志的重大贡献。已根据编号选择审阅者，过去12个月完成的报告的及时性和质量。我们想说[…] <p><strong>2017年的杰出评审员<em>medchemcomm</em>in 2017</strong><p>we would like to highlight the outstanding reviewers for<em><strong>medchemcomm</strong><em>in 2017，根据编辑组的选择，因为他们对杂志的重大贡献。已根据编号选择审阅者，过去12个月内完成的报告的及时性和质量。<p>We would like to say a big thank you to those personals listed here as well to all of the reviewers that have supported the journal.每位优秀的评审员都将收到一份证书，以表彰他们的重大贡献。<p>Dr Andreas Brunschweiger，Tu Dortmund，Germany，<a href=“http://orcid.org/0000-0002-4401-1495”>orcid:0000-0002-4401-1495</a><br/>Dr David Colby，University of Mississippi，USA，<a href=“http://orcid.org/0000-0002-5434-1690“>orcid:0000-0002-5434-1690<a><br/>教授Paul Furtm_ller，Boku大学自然资源与生命科学，奥地利，<a href=“http://orcid.org/0000-0002-1199-2469”>orcid:0000-0002-1199-2469<a><br/>Dr Keith Green，University of Kentucky，USA<br/>Dr Ke新利手机客户端 Jiang，Stanford University，美国<br/>Mukulesh Mondal博士，奥克兰大学，美国<br/>康塞普西翁博士桑切斯·马丁内斯，莉莉，西班牙，；<a href=“https://orcid.org/0000-0003-0221-497x”>orcid:0000-0003-0221-497x<<br/>教授；Mike；Waring，纽堡大学，英国，；<a href=“https://orcid.org/0000-0002-9110-8783”>orcid:0000-0002-9110-8783<a><br/>博士；志强；于，；南方医科大学，；中国，；<br/>博士160;博士；中国，中国，；<br/>博士岁叶_张，广西师范大学，中国，<a href=“http://orcid.org/0000-0002-6903-5602”>orcid:0000-0002-6903-5602</a>><p>we would also like to thank the<em>medchemcomm</em>board and the wider community for their continued support of the journal，作为作者，审阅者和读者。<p><p>如果您想成为我们的日志的审阅者，您可以在<a href=“http://www.rsc.org/journals books 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我们很高兴地宣布。Gon_alo Bernardes被选为2018年Medchemcomm新兴研究者讲师。该讲师对2008年或之后获得博士学位并在其早期职业生涯中对药物化学做出重大贡献的任何候选人开放。新利手机客户端编委会认为他的实质性的 <p>我们很高兴地宣布Gon_alo Bernardes</strong>已被选中接受2018年的医学博士学位，Emerging Investor Teacheship</p><p>The Teacheship was open to any candidate who received their phd in 2008 or later and have made a significant contribution to medical chemistry in their early career.新利手机客户端编委会认为他在蛋白质结合物化学方面做出了重大贡献，新利手机客户端他对抗体结合物领域的影响使他成为今年演讲的最佳选择。<p>on being informed of his selection dr.Bernardes说：<p><p><a href=“//www.xcmww.com/md/files/2018/02/gon_alo bernardes.jpg”><img class=“Alignright wp-image-2906”src=“//www.xcmww.com/md/files/2018/02/gon_alo-bernardes-829x1024.jpg”alt=“”width=“245”height=“303”srcset=“//www.xcmww.com/md/files/2018/02/gon_alo-bernardes-829x1024.jpg 829w，//www.xcmww.com/md/files/2018/02/gon_alo-bernardes-243x300.jpg 243w，//www.xcmww.com/md/files/2018/02/gon_alo-bernardes-768x948.jpg 768W，//www.xcmww.com/md/files/2018/02/gon_alo-bernardes.jpg 945w“尺寸=”（最大宽度：245px）100vw，245px“/>”<a>“<em>我很荣幸能从一个我非常钦佩的组织那里获得这一殊荣，因此我为我在剑桥和IMM里斯本的整个研究小组的工作感到无比自豪。<p>dr.Bernardes将在今年晚些时候的会议上发表演讲，以供确认。<p><span style=“text-decoration:underline”>about dr.Gon_alo bernardes</span>><p>dr.Gon_alo Bernardes是化学系的组长，新利手机客户端剑桥大学英国他还是医学分子研究所化学生物学和药物生物技术部主任，葡萄牙。在完成他的D.Phil之后。2008年毕业于牛津大学，英国他在马克斯普朗克胶体与界面研究所从事博士后工作。德国ETH Z_富，瑞士，并在葡萄牙阿尔法玛LDA担任组长。2013年，他开始了自己的独立研究生涯，他的研究小组主要通过使用化学原理来解决一系列对理解和对抗人类疾病具有重要意义的生物学问题。他是英国皇家学会大学的研究员，也是欧洲研究理事会（TAGIT）的一项启动拨款的获得者。<p><p><a href=“http://gbernardslab.com/research/“><strong>访问Gon_alo新利手机客户端's homepage以了解关于他正在进行的研究的更多信息。<strong><a><p><div class=“lightsocial_container”><a class=“lightsocial_a”href=“http://digg.com/submit”？url=http%3a%2f%2fwww.xcmww.com%2fmd%2f2018%2f02%2f26%2fdr-goncalo-bernardes-wins-the-2018-emerging-researcher-teacheship%2f&title=dr.+gon%c3%a7alo+bernardes+wins+the+2018+emerging+researcher+teacheship“><img class=“light social_img”src=“//www.xcmww.com/md/wp-content/plugins/light-social/digg.png”alt=“digg 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journals/medchemcomm/”><em>medchemcomm<em><a>articles in april，2017年5月和6月。<p><h4>回顾文章：<a href=“http://www.rsc.org/journals books databases/about journals/medchemcomm/”><img class=“Alignright wp-image-2900 size medium”src=“//www.xcmww.com/md/files/2017/10/mcc-cover-228x300.jpg”alt=“”width=“228”height=“300”srcset=“//www.xcmww.com/md/files/2017/10/mcc-cover-228x300.jpg 228W，//www.xcmww.com/md/files/2017/10/mcc-cover-768x1011.jpg 768W，//www.xcmww.com/md/files/2017/10/mcc-cover-778x1024.jpg 778w“尺寸=”（最大宽度：228px）100vw，228px”/>=<a><h4><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c4md00143e“>作为疫苗和潜在候选药物的多价糖缀合物Mathias Dimde and Rainer Haag<br/>doi:10.1039/c4md00143e</p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c4md00088a“>用于描述细菌多糖抗原的表面等离子体共振：a review<a>><strong>><br/>barbarbara brogioni and francesco berti<br/>doi:10.1039/c4md00088a<p>><strong>><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00232c“>抗菌剂的合理设计和优化的最新进展</a><strong><br/>jesse a.琼斯，克里斯托弗GVirgaGiuseppe Gumina和Kirk E.hevener<br/>doi:10.1039/c6md00232c<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c4md00216d“>使用蛋白质化学（pcm）的多药理学建模：最新方法学进展，目标家庭的申请，和未来的潜在客户Qurrat-ul-Ain，维涅什瓦里·萨布拉曼尼亚，鳗鱼B。Lenselink公司，奥斯卡·M·恩德斯·卢西奥，阿德里安P.伊泽曼Gerd WohlfahrtPeteris Prusis第二E。马尔利亚文，热拉尔J。P.van westen and andreas bender<br/>doi:10.1039/c4md00216d<p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00581k“>蛋白质-配体（un）结合动力学是在实验和建模之间的十字路口发现药物的一个新范例.<strong><br/>m.伯内蒂，a.卡瓦利和L。mollica<br/>doi:10.1039/c6md00581k<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c4md00269e“>蛋白质精氨酸甲基转移酶的结构生物学和化学-<a><s新利手机客户端trong><br/>matthieu schapira and renato ferreira de freitas<br/>doi:10.1039/c4md00269e-<p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00347h“>小分子介导的蛋白质敲除作为药物发现的新方法</a>><strong><br/>Christopher P.TinworthHannah Lithgow and Ian Churcher<br/>doi:10.1039/c6md00347h<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00373g“>BET家族外溴域的化学探针和抑制剂彼得G。K.克拉克，邓肯AHay戴伦J。狄克逊和保罗E。brennan<br/>doi:10.1039/c6md00373g<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c4md00085d“>用于受控释放的两亲性设计纳米载体：from drug delivery to diagnostics</a><strong><br/>Malinda Salim，小川弘，Akihiko Sugimura and Rauzah Hashim<br/>doi:10.1039/c4md00085d</p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c5md00303b“>2-[<sup>18<sup>f]氟乙基甲苯磺酸酯–a versatives toslate toolution for building<sup>18<sup>f-based radiotracers for positon emission tomography.<a><strong><br/>torsten kniess，马库斯·劳伯，Peter Brust and J_rg Steinbach<br/>doi:10.1039/c5md00303b</p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00607h“>许多圆形和无铅细菌素的结构特征类似于saposin和saposin-like peptides中的那些。MTowle和J.C.vederas<br/>doi:10.1039/c6md00607h<p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c5md00503e“>细菌脂质膜是抗微生物耐药性的理想靶点，通过更新氨基糖苷类抗生素和出现两亲性氨基糖苷的分子基础和图解doi=10.1039/c4md00131a“>朝向通过钉合肽了解细胞渗透</a><strong><br/>qian chu，雷蒙德E.莫勒林热拉尔J。希林斯基，Young Woo Kim汤姆N。Grossmann约翰内斯T.-H.Yeh和Gregory L.凡尔丁<br/>doi:10.1039/c4md00131a</p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00243a“>基于苯二氮卓和吡唑嘧啶支架的DNA编码库的设计和合成.<strong><br/>m.克里卡·科皮，OBugainK.JungS.OnsteinS.BrandhermTKalliokoski和A.brunschweiger<br/>doi:10.1039/c6md00243a</p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c5md00475f“>蛋白质表面聚乙二醇化的方法under structure reservation for the malute based formation of stable nandoms.<a><strong><br/>lydia radi，Matthias FachMirko Montigny埃琳娜·伯杰·尼科莱蒂，Wolfgang Tremel和Peter R.wich<br/>doi:10.1039/c5md00475f<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00560h“>Identification of midazo[1,2-<em>b<em>]pydazine tyk2 pseudokinase配体as potential and selective allosteric inhibitors of tyk2 signaling<a><strong><b r/>r.莫斯林D.加德纳，J.桑特拉，是的。张，J.五.德乔亚C.线路接口单元，J.林，J.S.托卡斯基，J.StrnadD.修脚师，J.陈，是的。布拉特，a.Zupa FernandezL.程H.太阳，C.乔杜里C.黄，C.达里安佐J.S.麻袋，J.K.穆克鲍尔，C.青稞酒，J.重复播放，D.解N.AranibarJ.R.BurkeP.H.卡特和D。S.weinstein<br/>doi:10.1039/c6md00560h</p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00648e“>探索Peptoid抗菌活性和毒性之间的联系</a>><strong>><br/>h.L.螺栓，G.a.爱格曼，C.a.B.JahodaR.N.ZuckermannG.J.Sharples与SL.cobb<br/>doi:10.1039/c6md00648e<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00637j“><em>nonomuraea<em>sp.ATCC 55076含有迄今为止最大的放线菌染色体和kistamicin生物合成基因簇克拉丽莎Forneris马库斯岛吉布森，皎月，凯尔西·R。Schrama和Mohammad R.seyedsayamdost<br/>doi:10.1039/c6md00637j<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c5md00022j“>G蛋白偶联组胺H的片段样配体的基于结构的虚拟筛选h<sub>4<sub>receptor<a><strong><br/>enade p.伊斯蒂亚斯托诺，艾伯特J.库伊斯特拉，亨利FVischerMartien KuijerLuc RoumenSaskia Nijmeijer，罗吉尔A史密斯，伊万JP.德埃斯许，rob leurs and chris de graaf<br/>doi:10.1039/c5md00022j<p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00231e“>人溶酶体酸脂肪酶抑制剂lalistat disabilities<em>mycobacterium tuberculosis.<em>growth by targeting bacterium hydrolasses.<a><strong><br/>j.莱曼J.沃马茨卡K.埃瑟，M诺德韦尔，K.科尔比，P.R，美国普罗策，N.瑞玲和Sa.sieber<br/>doi:10.1039/c6md00231e<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c5md00152h“>BRD7和BRD9溴域的强效和选择性抑制剂的设计和合成.<strong><br/>Duncan A.Hay凯瑟琳M。罗杰斯奥列格费多洛夫，辛西娅·塔伦特，莎拉·马丁，欧诺维亚蒙特罗，苏珊娜·米勒，斯蒂芬·克纳普，克里斯托弗J。斯科菲尔德和保罗E。brennan<br/>doi:10.1039/c5md00152h<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c4md00057a“>焓的基本视图–熵补偿</a><strong><br/>ulf ryde<br/>doi:10.1039/c4md00057a<p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c4md00291a“>优化基于三唑吡啶的组蛋白脱甲基酶抑制剂可生成有效且选择性的kdm2a（fbxl11）抑制剂</a><strong><br/>Katherine S。英国Anthony Tumber托比亚斯·克罗杰，朱塞佩·斯科扎法瓦，斯坦利S天然气，米歇尔·丹尼尔，亚历山德拉·西考夫斯卡，KaHing Che弗兰克·冯·德尔夫，尼古拉A。Burgess BrownAkane Kawamura克里斯托弗J。斯科菲尔德和保罗E。brennan<br/>doi:10.1039/c4md00291a<p><p><strong><a href=“http://xlink.rsc.org/？doi=10.1039/c6md00207b“>从链接的开放数据到分子相互作用：研究人类血清素和多巴胺转运体配体的选择性趋势伊娃·赫尔斯伯格，Michael Viereck和Gerhard F.ecker<br/>doi:10.1039/c6md00207b<p>keep-up-to-date with the latest issues 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//www.xcmww.com/md/？P＝2888 2018年Medchemcomm新兴研究者演讲现已开放提名。提名将于2017年11月28日结束。在2018年的一次会议上发言时，讲师的接受者将获得高达1000英镑的捐款。资格：讲师资格对2008年或之后获得博士学位并拥有[…]学位的候选人开放。 <p>2018年的Medchemcomm<em>Emerging Investiger讲师现在开始提名。<p><p><strong>提名将于2017年11月28日结束。<strong><p><p>The Recipient of the Teacheship will receive a contribution of up to英镑1000 to speaking at a conference in 2018.<p><table style=“background color:ffffff99”><tbody><tr style=“heright:288px“><td style=“height:288px”><strong>Qualification=>strong>讲师职位对2008年或之后获得博士学位，并在其早期职业生涯中对药物化学做出重大贡献的候选人开放，新利手机客户端尤其是如果他们给药物发现带来了新的想法。<p><p><strong>How you can insigned</strong>if you want to insign someone please email us（medchemcomm-rsc@rsc.org）with the following details:<p><ul><li>their name</li><li>their affiliation</li><li><u>at least</u>one paragraph explaining their responsibilities and why you think他们应该被考虑例如他们的简历，很有助于做出决定，但不是作出提名的强制要求。<p><p>self-insignations are accepted but<u>must</u>be supported by a letter of support from your departments head of 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周五，2017年2月24日10:00:29+0000 凯里·波特 新闻 医学化学通讯 //www.xcmww.com/md/？P=2881 继2016年9月同行评审周（致力于评审员认可）成功后，我们在该周内公布了一份顶级评审员名单，我们将继续通过每年公布我们的杰出审稿人来认可我们的审稿人对期刊所做的贡献。2016年Medchemcomm杰出评审，由[…]选择 <p>继2016年9月同行评审周（致力于评审员认可）成功后，我们在该周内公布了一份顶级评审员名单，我们将继续通过每年宣布我们的杰出审稿人来认可我们的审稿人对期刊所做的贡献。<p>Outstanding reviewers for<em>Medchemcomm<em>in 2016，根据编辑组的选择，已根据号码选择，过去12个月内完成的报告的及时性和质量。<p>a big thank you to those persons listed here as well to all of the reviewers that have supported the journal.每位优秀的评审员将收到一份证书，以表彰他们的重大贡献。<p>Dr Simone Carradori，Chieti Pescara大学科尔比，密西西比大学乔治亚州立大学张建村博士，中国科学院李正奎教授，新利手机客户端济南大学中国科学院新利手机客户端波恩大学伦敦帝国理工学院Kissei制药公司有限公司中国科学院也要感谢医学化学委员会和医药新利手机客户端化学界对该期刊的持续支持，新利手机客户端作为作者，评论人和读者。<p>如果你想成为我们期刊的评论人，只需<a href=“mailto:medchemcomm%20（shared）%20%3cmedchemcomm@rsc.org%3e”>向我们发送电子邮件，说明您的研究兴趣和最新的简历或R_sum_的详细信息。您可以在<a href=“http://www.rsc.org/journals books databases/journal authors reviewers/reviewer responsibilities/being 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href=“https://www.universitietleiden.nl/en/staffmembers/laura heitman”>laura h博士。来自莱顿大学的Heitman，荷兰2017年《新兴研究者演讲》的接收者在2007年或之后获得博士学位并在其早期职业生涯中对药物化学做出了重大贡献的任何候选人都可以获得讲师资格。新利手机客户端然后，编辑委员会对提名名单进行了投票。<p><p>许多人祝贺Dr.海特曼赢得了演讲权。由于目前的情况，博士。Heitman将寻求在2018年做她的演讲。<p><p><a href=“https://www.universitetleiden.nl/en/staffmembers/laura heitman”><img class=“AlignRight”src=“https://www.universitetleiden.nl/binaries/content/gallery/ul2/images/science/h/laura-heitman.jpg/laura-heitm新利手机客户端an.jpg/d200x250”width=“168”height=“210”/>.<p><p><p><p><span style=“text decoration:underline”><strong>about laura</strong><p><p>laura h.海特曼，博士。是莱顿药物研究学术中心（LacDr，新利手机客户端莱顿大学）2009年1月被任命为“终身制”助理教授。她于2009年4月获得了博士学位，与ORGANON/MSD（OSS，荷兰）。她的研究兴趣主要集中在理解和改善药物受体相互作用上，更具体地说，GPCRS的靶结合动力学和变构调控。在过去的几年里，她已获得多项竞争性研究资助（例如药物发现的IMI动力学/K4DD）都让她研究这些小说，药物作用的临床相关和高度转化概念。她的研究活动目前已经在这一领域的50多篇论文中产生了作者。包括一个在科学（2012年）和一个新利手机客户端在自然（2016年）。<p><div class=“lightsocial_container”><a 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buzz（aka）。google reader）“title=”google buzz（aka.google reader）“/>.<a>.<div> //www.xcmww.com/md/2017/02/13/2017-medchemcomm-emerging-researcher-steacheship-winner/feed/ 零 //www.xcmww.com/md/2017/01/12/paster-prize-winner-at-the-8th-brazmedchem-symposium/ //www.xcmww.com/md/2017/01/12/paster-prize-winner-at-the-8th-brazmedchem-symposium/回复 清华大学，2017年1月12日12:07:44+0000 凯里·波特 会议 海报奖 医学化学通讯 //www.xcmww.com/md/？P=2852 祝贺2016年Brazmedchem研讨会海报奖得主。我们很高兴地向丹尼尔A颁奖。罗德里格斯（里约热内卢联邦大学拉斯比奥·乌弗杰；主管：Carlos M.fraga）他的海报：“新型N-酰肼类HDAC6/8双抑制剂的抗增殖活性和化学稳定性”，研讨会在Arma_o dos b_zios举行，里约[…] <img class=“wp-id=“attach”style=“width:197px”class=“wp-capCapCapCapCapCapitaAlignright“><a href=“http://blog.rsc.org/md/file/2017/01/20161130_.jpg”><img class=“wp-image-2853”src=“http://blog.rsc.org/md/文件/2017/01/20161130_-E1484225252962-E1484225252963-238x300.jpg”wid=“187”height=“187”height=“236”srcsset=“http://blog.rsc.org/web/md/md/md/文件/2017/2017/01/01/20161130-14562-E14848484848422229363-238x300.JPG 238W，//www.xcmww.com/md/files/2017/01/20161130 U 14562-E148422529363.jpg 653w“尺寸=”（最大宽度：187px）100vw，187px“/><a><p class=“wp caption text”>daniel receiving his prize from prof.Koen Augustyns of<em>Medchemcomm</em>s editional board<p><div><p>恭喜海报奖获得者at the<a href=“http://brazmedchem2016.com.br/”>brazmedchem symposium 2016.<a><p>we were suppressed to present a prize to<strong>daniel a.罗德里格斯（Rodrigues）.<strong>（里约热内卢联邦大学lassbio ufrj；主管：Carlos M.fraga）对于他的海报：<p><p>“anti-proliferative activity and chemical stability of novel<em>n<em>-acylhydrazones dual inhibitors of hdac6/8”<p><p>The symposium happed place in arma_o dos b_zios，2016年11月27-30日，里约热内卢。有关该事件的简短视频摘要，请参见<a href=“https://youtu.be/lri-nmnx5om”>https://youtu.be/lri-nmnx5om<a><p><p>The main goal of brazmedchem2016 was to provide a scientific atmosphere to improve the cooperation between scientifics from brazil and abroad.为了应对二十一世纪药物化学的挑战，促进研究人员之间的经验和信息交流是至关重要的。<p><p><p><div class=“lightsocial”container“><a 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