首页> 外文OA文献 >Synthesis and Pharmacological Evaluation of Novel 9- and 10-Substituted Cytisine Derivatives. Nicotinic Ligands of Enhanced Subtype Selectivity

【2h】

Synthesis and Pharmacological Evaluation of Novel 9- and 10-Substituted Cytisine Derivatives. Nicotinic Ligands of Enhanced Subtype Selectivity

机译：新型9-和10取代的细胞苷衍生物的合成与药理评价。增强亚型选择性的尼古丁配体

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
Sheela K. Chellappan; Yingxian Xiao; Werner Tueckmantel; Kenneth J. Kellar; Alan P. Kozikowski;
展开▼
作者单位

展开▼
年度 2006
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. Synthesis and pharmacological evaluation of novel 9-and 10-substituted cytisine derivatives. Nicotinic ligands of enhanced subtype selectivity [J] . Chellappan SK, Xiao YX, Tueckmantel W, Journal of Medicinal Chemistry . 2006,第9期

机译：新型9-和10-取代的胱氨酸衍生物的合成和药理评价。增强亚型选择性的烟碱配体
2. Chemical Medicine: Novel 10-Substituted Cytisine Derivatives with Increased Selectivity for alpha4beta2 Nicotinic Acetylcholine Receptors [J] . Alan P. Kozikowski, Sheela K. Chellappan, Yingxian Xiao ChemMedChem . 2007,第8期

机译：化学医学：新型10位取代的胱氨酸衍生物，对alpha4beta2烟碱乙酰胆碱受体具有更高的选择性
3. Synthesis, Binding, and Modeling Studies of New Cytisine Derivatives, as Ligands for Neuronal Nicotinic Acetylcholine Receptor Subtypes [J] . Tasso B, Boido CC, Terranova E, Journal of Medicinal Chemistry . 2009,第14期

机译：作为神经元烟碱乙酰胆碱受体亚型的配体的新型胱氨酸衍生物的合成，结合和模型研究
4. Discovery, sequencing and synthesis optimization of a highly selective ligand binding an orphan adrenoreceptor subtype in the green mamba venom [C] . Loic Quinton, Celine Rouget, Gilles Mourier, ASMS Conference on Mass Spectrometry and Allied Topics . 2008

机译：高精度配体的发现，测序和合成优化在绿色曼巴纳毒液中结合孤儿肾上腺素亚型的高度选择性配体结合
5. Part One. Synthesis of optically active tryptophan derivatives with potential activity as indoleamine 2,3-dioxygenase inhibitors: An approach via asymmetric catalytic hydrogenation. Part Two. Design, synthesis and pharmacology of selective ligands for alpha1-containing GABA(A)/benzodiazepine receptor subtypes: SAR studies of beta-carbolines at positions -3 and -6 and their corresponding bivalent ligands. Part Three. First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A. [D] . Yin, Wenyuan. 2007

机译：第一部分。具有吲哚胺2,3-二加氧酶抑制剂潜在活性的旋光色氨酸衍生物的合成：一种通过不对称催化氢化的方法。第二部分。含α1的GABA（A）/苯并二氮杂receptor受体亚型的选择性配体的设计，合成和药理作用：位于-3和-6位的β-咔啉及其相应的二价配体的SAR研究。第三部分。重要生物遗传中间体，（+）-聚神经氨酸和（+）-聚神经氨酸醛，以及16-表-维西辛和Macusine A的首次对映体全合成。
6. Synthesis and Pharmacological Evaluation of Novel 9- and 10- Substituted Cytisine Derivatives - Nicotinic Ligands of Enhanced Subtype Selectivity [O] . Sheela K. Chellappan, Yingxian Xiao, Werner Tueckmantel, -1

机译：新型9和10-取代的胱氨酸衍生物-增强亚型选择性的烟碱配体的合成和药理评价
7. Synthesis and Pharmacological Evaluation of Novel 9- and 10-Substituted Cytisine Derivatives. Nicotinic Ligands of Enhanced Subtype Selectivity [O] . -1

机译：新型9-和10取代的细胞苷衍生物的合成与药理评价。增强亚型选择性的尼古丁配体
8. Chiral Synthesis via Organoboranes. 15. Selective Reductions. 42. Asymmetric Reduction of Representative Prochiral Ketones with Potassium 9-O-(1,2:5,6-Di-O-isopropylidene-alpha-D-glucofuranosyl)-9- boratabicyclo(3.3.1)-nonane [R] . Brown, H. C., Cho, B. T., Park, W. S. 1988

机译：有机硼烷的手性合成。 15.选择性减少。 42.用9-O-（1,2：5,6-二-O-异亚丙基-α-D-葡呋喃糖基）-9-硼三环（3.3.1） - 壬烷钾不对称还原代表性前手性酮

Synthesis and Pharmacological Evaluation of Novel 9- and 10-Substituted Cytisine Derivatives. Nicotinic Ligands of Enhanced Subtype Selectivity

著录项

引文网络

相似文献

相关主题

期刊订阅