Comparison of the inhibition potential of parthenolide and micheliolide on various UDP-glucuronosyltransferase isoforms-Reference-Cited by-同舟云学术

Comparison of the inhibition potential of parthenolide and micheliolide on various UDP-glucuronosyltransferase isoforms

Published:2019-04-25 Issue:10 Volume:49 Page:1158-1163
ISSN:0049-8254
Container-title:Xenobiotica
language:en
Short-container-title:Xenobiotica

Author:

Gao Wei-Feng¹,Li Yi-Xuan¹²,Zhang Wei-Hua¹,Tao Ran³,Yin Ting-Ting²,Wang Yi-Jia⁴,Liu Li-Na¹,Fu Zhi-Wei⁵,Li Sai-Nan⁵,Liu Nai-Rong⁵,Zhang Heng⁶,Liu Guang⁶,Zhao Li-Zhong¹,Zhang Xi-Peng¹,Zhang Chun-Ze¹

Affiliation:

1. Department of Colorectal Surgery, Tianjin Union Medical Center, Tianjin, China;

2. Department of Clinical Science of Integrated TCM and Western Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China;

3. Basic Medical College, Hebei North University, Hebei, China;

4. Department of Pathology, Tianjin Union Medical Center, Tianjin, China;

5. Department of Toxicology School of Public Health, Tianjin Medical University, Tianjin, China;

6. Tianjin Union Medical Center, Tianjin, China

Funder

the 13th five year plan and TMU talent project

National Natural Science Foundation of China

the China Postdoctoral Science Foundation

Tianjin Health Bureau Science Foundation Key Project

Postgraduate Innovation Fund of ‘13th Five-Year comprehensive investment’, Tianjin Medical University

Publisher

Informa UK Limited

Subject

Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/00498254.2018.1544383

Reference37 articles.

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2. The permeability characteristics and interaction of main components from Si-Ni-San in a MDCK epithelial cell monolayer model

3. Intestinal glucuronidation protects against chemotherapy-induced toxicity by irinotecan (CPT-11)

4. UDP-glucuronosyltransferase 2B15 (UGT2B15) and UGT2B17 Enzymes Are Major Determinants of the Androgen Response in Prostate Cancer LNCaP Cells

5. Cell context-dependent activities of parthenolide in primary and metastatic melanoma cells

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