1.
Identification of Compounds Targeting Pgp from Substituted Quinoxalinones and the Activity of QA3 to Reverse MDR of Cancer Cells
喹喔啉酮类化合物逆转多药耐药作用及QA3逆转机制研究
2.
Synthesis and Structure-activity Relationships of Quinoxaline Compounds;
喹喔啉类化合物的合成及构效关系研究
3.
Synthesis and Property of Imidazolones and Triazoloquinazolinones;
咪唑啉酮与三唑并喹唑啉酮类化合物的合成与性质
4.
Developments of Indenoisoquinolines
茚并异喹啉酮类化合物及衍生物的研究进展
5.
An Improved Indium-Mediated Reductive Intramolecular Cyclization of 2-Nitrochalcones to Quinolines;
利用铟由2-硝基查尔酮合成喹啉类化合物
6.
Advances on the Synthesis and the Anti-HIV Activities of Quinolinones
喹啉酮类化合物的合成及抗HIV活性研究进展
7.
Research Progress on Synthesis of 3(4)-Substituted Quinazoline(one) Derivatives
3(4)-取代喹唑啉(酮)类化合物合成方法研究进展
8.
Synthesis and aldose reductase inhibitory activities of methylquinolinoneacetic acids
甲基喹啉酮乙酸类化合物的合成及其醛糖还原酶抑制活性
9.
Bromination Synthesis of 6-Amino-5-bromoquinoxaline
6-氨基-5-溴喹喔啉的溴化合成
10.
The Synthesis of New Heterocyclic Derivatives Containing 1,2,3-Triazol or Quinoxaline by 1,3-Dipolar Cycloaddition;
1，3-偶极环加成合成新型含1，2，3-三唑及喹喔啉类杂环衍生物
11.
Study on the Synthesis、Reacting System of Novel Derivatives of Di-N-oxoquinoxaline Formaldehyde and Their Biological Activity;
二氮氧化喹喔啉甲醛衍生物合成、反应体系及生物活性研究
12.
Syntheses of Glycosides Containing Imidazole, Triazine and Quinoxaline;
含咪唑环、三嗪环和喹喔啉环的糖苷化合物的合成
13.
A Simple Methods of Synthesis for Pyrrolo-Pyridines and Pyrrolo- quinolines;
吡咯并吡啶(喹啉)类化合物的简易合成
14.
Study on the Synthesis and Herbicidal Activity of Novel Derivatives of Di-N-oxide Quinoxaline Formaldehyde;
二氮氧化喹喔啉甲醛衍生物的合成及除草活性的研究Ⅰ
15.
Study on New Methods of Synthesis Isoflavonoids and 3,4-dihydro-2(1H) Quinolinone Derivatives;
异黄酮类化合物合成新方法及3，4-二氢-2（1H）-喹啉酮衍生物合成新方法研究
16.
Indium-mediated Reductive Intramolecular Cyclization of 2-Nitrochalcones to Quinolines;
利用金属铟由2-硝基查尔酮类化合物还原分子内环化合成喹啉类化合物
17.
The Genotoxicity of Quinoxalines to Mammalian Cells;
喹喔啉类药物对哺乳动物细胞的遗传毒性研究
18.
Design, Synthesis and Primary Evaluation of Quinoxalinone Derivatives as Potent Modulators of Multidrug Resistance
喹喔啉酮类P-糖蛋白抑制剂的设计、合成及逆转肿瘤多药耐药活性研究