alpha(2A)- AND alpha(2C)-ADRENOCEPTORS AS SIGNIFICANT TARGETS FOR DOPAMINE AND DOPAMINE RECEPTOR LIGANDS

Casado-Anguera V.; Sanchez-Soto M.; Moreno E.; Bender J.; Yano H.; Cai N. -S.; Meiler J.; Cortes A.; Ferre S.; Casado V

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alpha(2A)- AND alpha(2C)-ADRENOCEPTORS AS SIGNIFICANT TARGETS FOR DOPAMINE AND DOPAMINE RECEPTOR LIGANDS

机译：α（2a） - 和α（2c） - 一种rencoceptors作为多巴胺和多巴胺受体配体的重要靶标

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来源
《Basic & clinical pharmacology & toxicology.》 |2018年第2期|共2页
作者
Casado-Anguera V.; Sanchez-Soto M.; Moreno E.; Bender J.; Yano H.; Cai N. -S.; Meiler J.; Cortes A.; Ferre S.; Casado V;
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作者单位

Univ Barcelona Fac Biol Dept Biochem &

Mol Biomed Barcelona Spain;

Univ Barcelona Fac Biol Dept Biochem &

Mol Biomed Barcelona Spain;

Univ Barcelona Fac Biol Dept Biochem &

Mol Biomed Barcelona Spain;

Vanderbilt Univ Dept Pharmacol Nashville TN USA;

NIDA Integrat Neurobiol Sect Intramural Res Program NIH Baltimore MD USA;

NIDA Integrat Neurobiol Sect Intramural Res Program NIH Baltimore MD USA;

Vanderbilt Univ Dept Pharmacol Nashville TN USA;

Univ Barcelona Fac Biol Dept Biochem &

Mol Biomed Barcelona Spain;

NIDA Integrat Neurobiol Sect Intramural Res Program NIH Baltimore MD USA;

Univ Barcelona Fac Biol Dept Biochem &

Mol Biomed Barcelona Spain;

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正文语种 eng
中图分类药学;
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专利

1. alpha(2A)- AND alpha(2C)-ADRENOCEPTORS AS SIGNIFICANT TARGETS FOR DOPAMINE AND DOPAMINE RECEPTOR LIGANDS [J] . Casado-Anguera V., Sanchez-Soto M., Moreno E., Basic & clinical pharmacology & toxicology. . 2018,第Suppla2期

机译：α（2a） - 和α（2c） - 一种rencoceptors作为多巴胺和多巴胺受体配体的重要靶标
2. Ligand modulation of [S-35]GTP gamma S binding at human alpha(2A), alpha(2B) and alpha(2C) adrenoceptors [J] . Audinot V., Fabry N., Nicolas JP., Cellular Signalling . 2002,第10期

机译：[S-35] GTPγS在人alpha（2A），alpha（2B）和alpha（2C）肾上腺素受体上的配体调节
3. Meperidine, remifentanil and tramadol but not sufentanil interact with alpha(2)-adrenoceptors in alpha(2A)-, alpha(2B)- and alpha(2C)-adrenoceptor knock out mice brain. [J] . Hocker J, Weber B, Tonner PH, European Journal of Pharmacology: An International Journal . 2008,第1a3期

机译：哌替啶，瑞芬太尼和曲马多但舒芬太尼不与α（2A）-，α（2B）-和α（2C）-肾上腺素受体中的α（2）-肾上腺素受体相互作用，可敲除小鼠大脑。
4. Identification of peptide ligands for alpha4beta1 integrin receptor as potential targeting agents for non-hodgki's lymphoma [C] . Steven I.Park, Renil Manat, Brian Vikstrom, the International Peptide Symposium . 2001

机译：α4Beta1整合蛋白受体鉴定肽配体作为非Hodgki淋巴瘤的潜在靶向剂
5. Tumor necrosis factor-alpha (TNFalpha) and receptor activator of NFkappaB ligand (RANKL) regulate osteoclast activity: Potential therapeutic targets in wear debris-induced osteolysis. [D] . Flick, Lisa Marie. 2002

机译：肿瘤坏死因子-α（TNFalpha）和NFkappaB配体的受体激活剂（RANKL）调节破骨细胞活性：磨损碎片诱导的骨溶解的潜在治疗靶标。
6. PM488. Activation of Galphaq proteins coupled with dopamine D1-like receptor and alpha1-adrenoceptor in rat brain membranes [O] . Yuji Odagaki, Masakazu Kinoshita, Toshio Ota 2016

机译：PM488。 Galphaq蛋白与多巴胺D1样受体和alpha1肾上腺素受体在大鼠脑膜中的激活
7. A new, simple and robust radioligand binding method used to determine kinetic off-rate constants for unlabeled ligands. Application at alpha(2A)- and alpha(2C)-adrenoceptors [O] . Uhlén, Staffan, Schiöth, Helgi B., Jahnsen, Jan Anker 2016

机译：一种新的，简单而可靠的放射性配体结合方法，用于确定未标记配体的动力学失速常数。在alpha（2A）-和alpha（2C）-肾上腺素受体上的应用

alpha(2A)- AND alpha(2C)-ADRENOCEPTORS AS SIGNIFICANT TARGETS FOR DOPAMINE AND DOPAMINE RECEPTOR LIGANDS

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