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	1.	[Mechanism and action characteristics studies of a quinoxalinone compound against HIV-1 replication]. [electronic resource] by Ba, Ming-Yu Cao, Ying-Li Xu, Bai-Ling Guo, Ying Producer: 20160125 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Synthesis and activity evaluation of PARP-1 inhibitors with azaindole skeleton]. [electronic resource] by Zhou, Jie Zhu, Zhi-Xiang Chen, Xiao-Guang Xu, Bai-Ling Producer: 20160202 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Recent advances in the study of pin1 and its inhibitors]. [electronic resource] by Zhang, Chong-Jing Zhang, Zhi-Hui Xu, Bai-Ling Wang, Yu-Ling Producer: 20090810 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Recent advance in the discovery of allosteric inhibitors binding to the AMP site of fructose-1,6-bisphosphatase]. [electronic resource] by Li, Zhan-mei Bie, Jian-bo Song, Hong-rui Xu, Bai-ling Producer: 20130603 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	5.	[Design, synthesis and biological evaluation of novel 3-(2-oxo-2-substituted acetamido)benzamides as PARP-1 inhibitors]. [electronic resource] by Yin, Yu-wen Ji, Ming Cao, Ran Chen, Xiao-guang Xu, Bai-ling Producer: 20160202 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	6.	[Design, synthesis and biological evaluation of novel para-substituted 1-benzyl-quinazoline-2, 4 (1H, 3H)-diones as human PARP-1 inhibitors]. [electronic resource] by Yao, Hai-Ping Zhu, Zhi-Xiang Ji, Ming Chen, Xiao-Guang Xu, Bai-Ling Producer: 20160202 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	7.	[2,3-Dihydro-1H-pyrrolo[3,2-c]quinoline and 2,3,5,9b-tetrahydro-1H-pyrrolo[3,2-c]-quinoline derivatives:synthesis and their inhibitory activity against Kv2.1]. [electronic resource] by Liu, Dong Guo, Ting-ting Wang, Wei-ping Wang, Xiao-liang Xu, Bai-ling Producer: 20180810 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	8.	A novel derivative of quinazoline, WYK431 induces G2/M phase arrest and apoptosis in human gastric cancer BGC823 cells through the PI3K/Akt pathway. [electronic resource] by Wang, Tian-En Wang, Yong-Kang Jin, Jing Xu, Bai-Ling Chen, Xiao-Guang Producer: 20150126 In: International journal of oncology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	[Design, synthesis and biological evaluation of novel diaryl ethers bearing a pyrimidine motif as human Pin1 inhibitors]. [electronic resource] by Xi, Yue-Yue Jin, Jing Sun, Yan Chen, Xiao-Guang Song, Hong-Rui Xu, Bai-Ling Producer: 20160202 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	10.	Synthesis and antitumor activity of novel 2-(1-substituted-piperidin-4-ylamino)quinazolines as antitumor agents. [electronic resource] by Wang, Yong-Kang Jin, Jing Zhu, Li-Na Zhang, Yi Chen, Xiao-Guang Gao, Xin-Qin Xu, Bai-Ling Producer: 20131021 In: Yao xue xue bao = Acta pharmaceutica Sinica vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	11.	Synthesis and cytotoxic evaluation of N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-arylsulfonamide and N-aryl-(4-methoxy-1H-benzo[d]imidazol)-7-sulfonamide analogs of combretastatin A-4. [electronic resource] by Zhou, Jie Zhang, Yi Cui, Yi-Wen Li, Zhan-Mei Song, Hong-Rui Dong, Jin-Hua Chen, Xiao-Guang Xu, Bai-Ling Producer: 20110620 In: Journal of Asian natural products research vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)