نتایج جستجو برای: hydroxamic acids

تعداد نتایج: 265477  

Journal: :Chemical and Pharmaceutical Bulletin 1992

Journal: :The Journal of the Society of Chemical Industry, Japan 1957

Journal: :Global Journal of Pharmacy & Pharmaceutical Sciences 2018

Journal: :Organic & biomolecular chemistry 2014
Giovanna Dettori Silvia Gaspa Andrea Porcheddu Lidia De Luca

The first synthesis of hydroxamic acids from alcohols has been developed. Both benzylic and aliphatic alcohols can be tolerated and applied in this reaction. The methodology is economical, environmentally benign and high yielding.

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2014
masoud hojjatie subramaniam muralidharan saswait p.bag giris c.panda henry freiser

the effect of alkyl substituents on the c-phenyl and/or the n-phenyl ring of benzophenylhydroxamic acid on their molecular structure and hydrogen bonding has been investigated. the predominant configuration in chcl3 is determined by steric and electronic effects. substituents on the c-phenyl ring favor the cis configuration, while substituents in the n-phenyl ring favor a trans configuration. t...

2012
Fabrice PL Andrieux Colin Boxall Robin J Taylor

Simple hydroxamic acids (XHA) are hydrophilic organic compoundswith the general formula RCONHOH that can act as O,O donor ligands with high affinities for hard cations such as Fe3+, Np4+ and Pu4+ with which they form 5-membered chelate rings (Muri et al.,2002; Desaraju & Winston,1986; Carrott et al.,2007). They have a wide range of applications in many fields, including as enzyme inhibitors, so...

2015
Kevin B. Daniel Eric D. Sullivan Yao Chen Joshua C. Chan Patricia A. Jennings Carol A. Fierke Seth M. Cohen

Histone deacetylase inhibitors (HDACi) target abnormal epigenetic states associated with a variety of pathologies, including cancer. Here, the development of a prodrug of the canonical broad-spectrum HDACi suberoylanilide hydroxamic acid (SAHA) is described. Although hydroxamic acids are utilized universally in the development of metalloenzyme inhibitors, they are considered to be poor pharmaco...

Journal: :Bioorganic Chemistry 2021

LpxC inhibitors represent a promising class of novel antibiotics selectively combating Gram-negative bacteria. In chiral pool syntheses starting from D- and L-xylose, series four 2r,3c,4t-configured C-furanosidic was obtained. The synthesized hydroxamic acids were tested for antibacterial inhibitory activity, the acquired biological data compared with those previously C-furanosides, molecular d...

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