نتایج جستجو برای: hydroxamate

تعداد نتایج: 630  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
H Ton-That G Liu S K Mazmanian K F Faull O Schneewind

Surface proteins of Staphylococcus aureus are linked to the bacterial cell wall by sortase, an enzyme that cleaves polypeptides at the threonine of the LPXTG motif. Surface proteins can be released from staphylococci by treatment with hydroxylamine, resulting in the formation of threonine hydroxamate. Staphylococcal extracts, as well as purified sortase, catalyze the hydroxylaminolysis of pepti...

Journal: :Infection and immunity 1984
J Z Montgomerie A Bindereif J B Neilands G M Kalmanson L B Guze

Clinical isolates of Escherichia coli were examined for the presence of hydroxamate siderophore (aerobactin). The incidence of aerobactin-positive strains of E. coli from the blood was greater than the incidence of these strains isolated from other sites. The presence of aerobactin and the virulence of strains of E. coli in urinary tract infection were also examined in mice. The presence of aer...

2013
Antonino Grassadonia Pasquale Cioffi Felice Simiele Laura Iezzi Marinella Zilli Clara Natoli

Hydroxamate-based histone deacetylase inhibitors (Hb-HDACIs), such as vorinostat, belinostat and panobinostat, have been previously shown to have a wide range of activity in hematologic malignancies such as cutaneous T-cell lymphoma and multiple myeloma. Recent data show that they synergize with a variety of cytotoxic and molecular targeted agents in many different solid tumors, including breas...

2013
Takayoshi Suzuki Hiroki Ozasa Yukihiro Itoh Peng Zhan Hideyuki Sawada Koshiki Mino Louise Walport Rei Ohkubo Akane Kawamura Masato Yonezawa Yuichi Tsukada Anthony Tumber Hidehiko Nakagawa Makoto Hasegawa Ryuzo Sasaki Tamio Mizukami Christopher J. Schofield Naoki Miyata

Histone N(ε)-methyl lysine demethylases KDM2/7 have been identified as potential targets for cancer therapies. On the basis of the crystal structure of KDM7B, we designed and prepared a series of hydroxamate analogues bearing an alkyl chain. Enzyme assays revealed that compound 9 potently inhibits KDM2A, KDM7A, and KDM7B, with IC50s of 6.8, 0.2, and 1.2 μM, respectively. While inhibitors of KDM...

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