Borch Richard F相关文献与解析，生知库 | 链接生命科学的每一步

Design and synthesis of a potential SH2 domain inhibitor bearing a stereodiversified 1,4-cis-enediol scaffold

设计并合成一种具有立体多样化1,4-顺式-烯二醇骨架的潜在SH2结构域抑制剂

期刊:Tetrahedron

影响因子:2.2

doi:10.1016/j.tet.2011.10.014

Marian, Christine; Huang, Rong; Borch, Richard F

发表日期：2011

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A novel geranylgeranyl transferase inhibitor in combination with lovastatin inhibits proliferation and induces autophagy in STS-26T MPNST cells

一种新型香叶基香叶基转移酶抑制剂与洛伐他汀联合使用可抑制STS-26T MPNST细胞的增殖并诱导其自噬。

期刊:Journal of Pharmacology and Experimental Therapeutics

影响因子:3.8

doi:10.1124/jpet.109.160192

Sane, Komal M; Mynderse, Michelle; Lalonde, Daniel T; Dean, Ivory S; Wojtkowiak, Jonathan W; Fouad, Farid; Borch, Richard F; Reiners, John J Jr; Gibbs, Richard A; Mattingly, Raymond R

Role of the multifunctional DNA repair and redox signaling protein Ape1/Ref-1 in cancer and endothelial cells: small-molecule inhibition of the redox function of Ape1.

多功能DNA修复和氧化还原信号蛋白Ape1/Ref-1在癌症和内皮细胞中的作用：小分子抑制Ape1的氧化还原功能

期刊:Antioxidants & Redox Signaling

影响因子:6.1

doi:10.1089/ars.2008.2120

Luo Meihua, Delaplane Sarah, Jiang Aihua, Reed April, He Ying, Fishel Melissa, Nyland Rodney L 2nd, Borch Richard F, Qiao Xiaoxi, Georgiadis Millie M, Kelley Mark R

Highly efficient synthesis of enantiomerically enriched 2-hydroxymethylaziridines by enzymatic desymmetrization

通过酶促去对称化高效合成对映体富集的2-羟甲基氮丙啶

期刊:Organic Letters

影响因子:5

doi:10.1021/ol062643a

Choi, Jun Young; Borch, Richard F

发表日期：2007

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Synthesis of a phosphoserine mimetic prodrug with potent 14-3-3 protein inhibitory activity

合成一种具有强效14-3-3蛋白抑制活性的磷酸丝氨酸模拟前药

Design and synthesis of a potential SH2 domain inhibitor bearing a stereodiversified 1,4-cis-enediol scaffold

设计并合成一种具有立体多样化1,4-顺式-烯二醇骨架的潜在SH2结构域抑制剂

A novel geranylgeranyl transferase inhibitor in combination with lovastatin inhibits proliferation and induces autophagy in STS-26T MPNST cells

一种新型香叶基香叶基转移酶抑制剂与洛伐他汀联合使用可抑制STS-26T MPNST细胞的增殖并诱导其自噬。

Role of the multifunctional DNA repair and redox signaling protein Ape1/Ref-1 in cancer and endothelial cells: small-molecule inhibition of the redox function of Ape1.

多功能DNA修复和氧化还原信号蛋白Ape1/Ref-1在癌症和内皮细胞中的作用：小分子抑制Ape1的氧化还原功能

Highly efficient synthesis of enantiomerically enriched 2-hydroxymethylaziridines by enzymatic desymmetrization

通过酶促去对称化高效合成对映体富集的2-羟甲基氮丙啶