首页> 外文OA文献 >The Glutaminase Inhibitor Compound 968 Exhibits Potent in vitro and in vivo anti-tumor Effects in Endometrial Cancer

【2h】

The Glutaminase Inhibitor Compound 968 Exhibits Potent in vitro and in vivo anti-tumor Effects in Endometrial Cancer

机译：谷氨酰胺酶抑制剂化合物968在子宫内膜癌中表现出有效的体外和体内抗肿瘤作用

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
Lingqin Yuan; Hui Guo; Guoyou Pan; Cong Wang; Dapeng Li; Naifu Liu; Ling Wei; Peipei Li; Xiugui Sheng;
展开▼
作者单位

展开▼
年度 2020
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. L-4, a Well-Tolerated and Orally Active Inhibitor of Hedgehog Pathway, Exhibited Potent Anti-tumor Effects Against Medulloblastoma in vitro and in vivo [J] . Mingfei Zhu, Hong Wang, Chenglin Wang, Frontiers in Pharmacology . 2019,第8期

机译：L-4是一种耐受性强且口服的Hedgehog通路抑制剂，对髓母细胞瘤的体外抗癌作用显着在体外和在体内
2. Ferulin C triggers potent PAK1 and p21-mediated anti-tumor effects in breast cancer by inhibiting Tubulin polymerization in vitro and in vivo [J] . Yao Dahong, Pan Dabo, Zhen Yongqi, Pharmacological research: The official journal of The Italian Pharmacological Society . 2020,第期

机译：Ferulin C通过在体外和体内抑制细胞蛋白聚合来触发有效的PAK1和P21介导的乳腺癌的抗肿瘤作用
3. DAT-230, a novel microtubule inhibitor, exhibits potent anti-tumor activity by inducing G2/M phase arrest, apoptosis in vitro and perfusion decrease in vivo to HT-1080 [J] . QiaoF., ZuoD., ShenX., Cancer chemotherapy and pharmacology. . 2012,第2期

机译：DAT-230是一种新型微管抑制剂，通过诱导G2 / M期阻滞，体外细胞凋亡和体内灌注减少，对HT-1080具有有效的抗肿瘤活性。
4. Design, Synthesis, Biophysical and Structure-Activity Properties of a Novel Dual MDM2 and MDMX Targeting Stapled α-Helical Peptide: ATSP-7041 Exhibits Potent In Vitro and In Vivo Efficacy in Xenograft Models of Human Cancer [C] . V. Guerlavais, K. Darlak, B. Graves American Peptide Symposium . 2013

机译：新型双MDM2和MDMX靶向吻合α-螺旋肽的设计，合成，生物物理和结构 - 活性特性：ATSP-7041在体外表现出效率和体内人类癌症的模型
5. Briciclib (on 013105), an elF4E inhibitor, exhibits potent anti-cancer activity in various preclinical cancer models. [D] . Desai, Bina. 2015

机译：elF4E抑制剂Briciclib（在013105上）在各种临床前癌症模型中均显示出强大的抗癌活性。
6. L-4 a Well-Tolerated and Orally Active Inhibitor of Hedgehog Pathway Exhibited Potent Anti-tumor Effects Against Medulloblastoma in vitro and in vivo [O] . Mingfei Zhu, Hong Wang, Chenglin Wang, -1

机译：L-4刺猬通路的良好耐受性和口服活性抑制剂在体外和体内均显示出对髓母细胞瘤的有效抗肿瘤作用
7. Correction to “Bifunctional Naphtho2,3-d1,2,3triazole-4,9-dione Compounds Exhibit Antitumor Effects In Vitro and In Vivo by Inhibiting Dihydroorotate Dehydrogenase and Inducing Reactive Oxygen Species Production” [O] . Zeping Zuo, Xiaocong Liu, Xinying Qian, 2020

机译：通过抑制二氢脱氢酶和诱导反应性氧物质生产，校正“双官能萘2,3-D 1,2,3 1,2,3三唑-4,9-二酮化合物在体外和体内表现出抗肿瘤作用，并诱导反应性氧物种生产”

The Glutaminase Inhibitor Compound 968 Exhibits Potent in vitro and in vivo anti-tumor Effects in Endometrial Cancer

著录项

引文网络

相似文献

相关主题

期刊订阅