Junlin He

Polyphyllin I induces autophagy and cell cycle arrest via inhibiting PDK1/Akt/mTOR signal and downregulating cyclin B1 in human gastric carcinoma HGC-27 cells.

Cheng Peng, Ruo-qi Zhang, Jing-lan Wu, 2019, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Pharmacological Properties and Derivatives of Shikonin-A Review in Recent Years.

Cheng Peng, Miao Wang, Xiaominting Song, 2019, Pharmacological research.

Isoliquiritigenin, an orally available natural FLT3 inhibitor from licorice, exhibits selective anti-AML efficacy in vitro and in vivo

Fei Gao, Yvonne Ying-Ya Wen, Ruo-qi Zhang, 2019 .

Ameliorative effect of Atractylodes macrocephala essential oil combined with Panax ginseng total saponins on 5-fluorouracil induced diarrhea is associated with gut microbial modulation.

Cheng Peng, Wuwen Feng, Hui Ao, 2019, Journal of ethnopharmacology.

Isochromanes from Aspergillus fumigatus, an endophytic fungus from Cordyceps sinensis

Yucheng Gu, Yun Deng, Z. Cao, 2019, Natural product research.

Aryl-tetralin-type lignan isolated from Sanguisorba officinalis

Yucheng Gu, Yun Deng, Z. Cao, 2018, Journal of Asian natural products research.

Iridoids from Valeriana jatamansi induce autophagy-associated cell death via the PDK1/Akt/mTOR pathway in HCT116 human colorectal carcinoma cells.

Cheng Peng, Yuzhu Tan, Li-Xia Wang, 2019, Bioorganic chemistry.

Isoliquiritigenin, an Orally Available Natural FLT3 Inhibitor from Licorice, Exhibits Selective Anti–Acute Myeloid Leukemia Efficacy In Vitro and In Vivo

Cheng Peng, Y. Wen, Shurong Zheng, 2019, Molecular Pharmacology.

Aloe emodin induces hepatotoxicity by activating NF-κB inflammatory pathway and P53 apoptosis pathway in zebrafish.

Lihong Gong, Cheng Peng, Yunxia Li, 2019, Toxicology letters.

Erlotinib is effective against FLT3‐ITD mutant AML and helps to overcome intratumoral heterogeneity via targeting FLT3 and Lyn

Cheng Peng, F. Peng, Xiaominting Song, 2020, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

4,6-Substituted-1H-Indazoles as potent IDO1/TDO dual inhibitors.

Yang Chen, Fei Wang, Lingling Yang, 2019, Bioorganic & Medicinal Chemistry.