Moshe Finel相关文献与解析，生知库 | 链接生命科学的每一步

Molecular Docking-Based Design and Development of a Highly Selective Probe Substrate for UDP-glucuronosyltransferase 1A10

基于分子对接的 UDP-葡萄糖醛酸转移酶 1A10 高选择性探针底物的设计和开发

doi:10.1021/acs.molpharmaceut.7b00871

Risto O Juvonen, Sanna Rauhamäki, Sami Kortet, Sanna Niinivehmas, Johanna Troberg, Aleksanteri Petsalo, Juhani Huuskonen, Hannu Raunio, Moshe Finel, Olli T Pentikäinen

信号转导

发表日期：2018

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Albumin stimulates the activity of the human UDP-glucuronosyltransferases 1A7, 1A8, 1A10, 2A1 and 2B15, but the effects are enzyme and substrate dependent

白蛋白可刺激人类 UDP-葡萄糖醛酸转移酶 1A7、1A8、1A10、2A1 和 2B15 的活性，但其作用依赖于酶和底物

期刊:PLoS One

影响因子:2.9

doi:10.1371/journal.pone.0054767

Nenad Manevski, Johanna Troberg, Paolo Svaluto-Moreolo, Klaudyna Dziedzic, Jari Yli-Kauhaluoma, Moshe Finel

Role of human UDP-glucuronosyltransferases in the biotransformation of the triazoloacridinone and imidazoacridinone antitumor agents C-1305 and C-1311: highly selective substrates for UGT1A10

人类 UDP-葡萄糖醛酸转移酶在三唑并吖啶酮和咪唑并吖啶酮抗肿瘤药物 C-1305 和 C-1311 的生物转化中的作用：UGT1A10 的高选择性底物

期刊:Drug Metabolism and Disposition

影响因子:4.4

doi:10.1124/dmd.112.045401

Barbara Fedejko-Kap, Stacie M Bratton, Moshe Finel, Anna Radominska-Pandya, Zofia Mazerska

Analysis of R- and S-hydroxywarfarin glucuronidation catalyzed by human liver microsomes and recombinant UDP-glucuronosyltransferases

人肝微粒体和重组UDP-葡萄糖醛酸转移酶催化的R-和S-羟基华法林葡萄糖醛酸化分析

期刊:Journal of Pharmacology and Experimental Therapeutics

影响因子:3.1

doi:10.1124/jpet.111.184721

Stacie M Bratton, Carrie M Mosher, Farid Khallouki, Moshe Finel, Michael H Court, Jeffery H Moran, Anna Radominska-Pandya

发表日期：2012

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Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases

人类 UDP-葡萄糖醛酸转移酶对裸盖菇素和 4-羟基吲哚进行葡萄糖醛酸化

期刊:Drug Metabolism and Disposition

影响因子:4.4

doi:10.1124/dmd.109.031138

Nenad Manevski, Mika Kurkela, Camilla Höglund, Timo Mauriala, Michael H Court, Jari Yli-Kauhaluoma, Moshe Finel

发表日期：2010

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Human UDP-glucuronosyltransferase UGT2A2: cDNA construction, expression, and functional characterization in comparison with UGT2A1 and UGT2A3

人类 UDP-葡萄糖醛酸转移酶 UGT2A2：与 UGT2A1 和 UGT2A3 相比的 cDNA 构建、表达和功能特征

期刊:Pharmacogenetics and Genomics

影响因子:1.7

doi:10.1097/FPC.0b013e3283330767

Nina Sneitz, Michael H Court, Xiuling Zhang, Kaisa Laajanen, Karen K Yee, Pamela Dalton, Xinxin Ding, Moshe Finel

Human

发表日期：2009

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Neobavaisoflavone Induces Bilirubin Metabolizing Enzyme UGT1A1 via PPARα and PPARγ

新巴伐利亚异黄酮通过 PPARα 和 PPARγ 诱导胆红素代谢酶 UGT1A1

An ultra-sensitive and easy-to-use assay for sensing human UGT1A1 activities in biological systems

一种超灵敏且易于使用的检测方法，用于检测生物系统中人类 UGT1A1 的活性

Molecular Docking-Based Design and Development of a Highly Selective Probe Substrate for UDP-glucuronosyltransferase 1A10

基于分子对接的 UDP-葡萄糖醛酸转移酶 1A10 高选择性探针底物的设计和开发

Albumin stimulates the activity of the human UDP-glucuronosyltransferases 1A7, 1A8, 1A10, 2A1 and 2B15, but the effects are enzyme and substrate dependent

白蛋白可刺激人类 UDP-葡萄糖醛酸转移酶 1A7、1A8、1A10、2A1 和 2B15 的活性，但其作用依赖于酶和底物

Role of human UDP-glucuronosyltransferases in the biotransformation of the triazoloacridinone and imidazoacridinone antitumor agents C-1305 and C-1311: highly selective substrates for UGT1A10

人类 UDP-葡萄糖醛酸转移酶在三唑并吖啶酮和咪唑并吖啶酮抗肿瘤药物 C-1305 和 C-1311 的生物转化中的作用：UGT1A10 的高选择性底物

Analysis of R- and S-hydroxywarfarin glucuronidation catalyzed by human liver microsomes and recombinant UDP-glucuronosyltransferases

人肝微粒体和重组UDP-葡萄糖醛酸转移酶催化的R-和S-羟基华法林葡萄糖醛酸化分析

Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases

人类 UDP-葡萄糖醛酸转移酶对裸盖菇素和 4-羟基吲哚进行葡萄糖醛酸化

Human UDP-glucuronosyltransferase UGT2A2: cDNA construction, expression, and functional characterization in comparison with UGT2A1 and UGT2A3

人类 UDP-葡萄糖醛酸转移酶 UGT2A2：与 UGT2A1 和 UGT2A3 相比的 cDNA 构建、表达和功能特征