Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1) (vol 707, pg 140, 2013)

Voss Marc D.; Zoller Gerhard; Matter Hans; Herling Andreas W.; Biemer-Daub Gabriele; Pfenninger Anja; Haag-Diergarten Silke; Keil Stefanie; Kohlmann Markus; Schmidts Hans-Ludwig

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Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1) (vol 707, pg 140, 2013)

机译：SAR707的发现和药理学表征作为硬脂酰-CoA去饱和酶（SCD1）的新型和选择性小分子抑制剂（体积707，PG 140,2013）

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来源
《European Journal of Pharmacology: An International Journal》 |2013年第3期|共2页
作者
Voss Marc D.; Zoller Gerhard; Matter Hans; Herling Andreas W.; Biemer-Daub Gabriele; Pfenninger Anja; Haag-Diergarten Silke; Keil Stefanie; Kohlmann Markus; Schmidts Hans-Ludwig;
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Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

Sanofi Aventis Res &

Dev Frankfurt Germany;

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正文语种 eng
中图分类药理学;
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1. Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1) (vol 707, pg 140, 2013) [J] . Voss Marc D., Zoller Gerhard, Matter Hans, European Journal of Pharmacology: An International Journal . 2013,第1a3期

机译：SAR707的发现和药理学表征作为硬脂酰-CoA去饱和酶（SCD1）的新型和选择性小分子抑制剂（体积707，PG 140,2013）
2. Erratum to "Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1)" [Eur. J. Pharmacol. 707 (1-3) (2013) 140-146] [J] . Marc D. Voss, Gerhard Zoller, Hans Matter, European Journal of Pharmacology: An International Journal . 2013,第1a3期

机译：错误“SAR707的发现和药理表征作为新型和选择性小分子抑制剂的硬脂酰-CoA去饱和酶（SCD1）”[EUR。 J. Pharmacol。 707（1-3）（2013）140-146]
3. Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1) [J] . VossM.D., ZollerG., MatterH., European Journal of Pharmacology: An International Journal . 2013,第1a3期

机译：作为硬脂酰辅酶A去饱和酶（SCD1）的新型选择性小分子抑制剂SAR707的发现和药理特性
4. Multi-Target Pharmacology of Small Molecule Drugs and First-In-Class Inhibitors Discovery [D] . Shi, Da. 2020

机译：小分子药物的多目标药理学和一流的抑制剂发现
5. Stearoyl-CoA Desaturase-1 (SCD1) Augments Saturated Fatty Acid-Induced Lipid Accumulation and Inhibits Apoptosis in Cardiac Myocytes [O] . Hiroki Matsui, Tomoyuki Yokoyama, Kenichi Sekiguchi, 2009

机译：硬脂酰辅酶A去饱和酶1（SCD1）增强饱和脂肪酸诱导的脂质蓄积并抑制心肌细胞的凋亡。
6. Stearoyl-CoA Desaturase-1 (SCD1) Augments Saturated Fatty Acid-Induced Lipid Accumulation and Inhibits Apoptosis in Cardiac Myocytes [O] . Matsui, Hiroki, Yokoyama, Tomoyuki, Sekiguchi, Kenichi, 2012

机译：硬脂酰辅酶A去饱和酶1（SCD1）增强饱和脂肪酸诱导的脂质蓄积并抑制心肌细胞的凋亡。

Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1) (vol 707, pg 140, 2013)

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