Catalyzed Synthesis of 3-hydroxy-indol-2-one Derivatives as a Novel Phosphodiesterases 10 Inhibitor
文献类型:期刊论文
作者 | Wu, Ya4; Li, Hao4; Yan, Jiao4; Cai, Qing4; Huang, Shengxiong3![]() ![]() |
刊名 | BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
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出版日期 | 2020-02-01 |
卷号 | 126页码:33-34 |
ISSN号 | 1742-7835 |
WOS研究方向 | Pharmacology & Pharmacy ; Toxicology |
语种 | 英语 |
WOS记录号 | WOS:000509492400043 |
源URL | [http://ir.kib.ac.cn/handle/151853/70837] ![]() |
专题 | 昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室 |
作者单位 | 1.Chinese Acad Sci, Guiyang, Guizhou, Peoples R China 2.Key Lab Chem Nat Prod Guizhou Prov, Guiyang, Guizhou, Peoples R China 3.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming, Yunnan, Peoples R China 4.Xian Shiyou Univ, Coll Chem & Chem Engn, Xian, Shaanxi, Peoples R China |
推荐引用方式 GB/T 7714 | Wu, Ya,Li, Hao,Yan, Jiao,et al. Catalyzed Synthesis of 3-hydroxy-indol-2-one Derivatives as a Novel Phosphodiesterases 10 Inhibitor[J]. BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY,2020,126:33-34. |
APA | Wu, Ya.,Li, Hao.,Yan, Jiao.,Cai, Qing.,Huang, Shengxiong.,...&Chen, Gang.(2020).Catalyzed Synthesis of 3-hydroxy-indol-2-one Derivatives as a Novel Phosphodiesterases 10 Inhibitor.BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY,126,33-34. |
MLA | Wu, Ya,et al."Catalyzed Synthesis of 3-hydroxy-indol-2-one Derivatives as a Novel Phosphodiesterases 10 Inhibitor".BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY 126(2020):33-34. |
入库方式: OAI收割
来源:昆明植物研究所
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