نتایج جستجو برای: o aminophenol

تعداد نتایج: 554926  

A. Badiei A. Banan G. Mohammadi Ziarani, M. Shakiba Nahad

Sulfonic acid functionalized SBA-15 as a nanoporous acid catalyst was used in the synthesis of 2-Aryl benzoxazoles 4 by the condensation of 2-aminophenol 1 and benzoyl chlorides 2 under microwave irradiation in solvent free reaction conditions. The advantages of this methodology are good product yields (60-98%), being environmentally benign, short reaction times and easy work up.

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2000
Z Yan J G Nikelly L Killmer J B Tarloff

Autoxidation of para-aminophenol (PAP) has been proposed to account for the selective nephrotoxicity of this compound. However, other studies suggest that hepatic metabolites of PAP rather than the parent compound may be responsible for renal damage. These studies were designed to investigate PAP metabolism in isolated hepatocytes. We synthesized several proposed metabolites for analysis by HPL...

Journal: :The Journal of biological chemistry 1952
S BERNSTEIN R W MCGILVERY

It has been demonstrated by many workers (l-5) that phenols may be conjugated with glucuronic acid or inorganic sulfate in vitro by liver slices and by cell-free preparations. By using a system developed in this laboratory, together with a modification of the analytical procedure described by Levvy and Storey (3), the synthesis of the conjugated sulfate, and possibly of the glucuronide, has bee...

Journal: :Journal of bacteriology 2007
Hirokazu Suzuki Yasuo Ohnishi Sueharu Horinouchi

An arylamine N-acetyltransferase (NAT) responsible for the N acetylation of exogenous 3-amino-4-hydroxybenzoic acid in Streptomyces griseus was identified and characterized. This enzyme was distinct from other eukaryotic and bacterial NATs in that it acetylated various 2-aminophenol derivatives more effectively than it acetylated 5-aminosalicylic acid, and thus it may be involved in the metabol...

Journal: :Molecules 2017
Jie Ma Chuang-Jun Li Jing-Zhi Yang Hua Sun Dong-Ming Zhang

A new phenylpropanoid glycoside (1), and two new coumarin glycosides (2, 3), together with two known compounds (4, 5), have been isolated from the stems of Hydrangea paniculata Sieb. Their structures have been determined by spectroscopic and chemical methods. Furthermore, compound 1 (50 μM) exhibited significant hepatoprotective activity against N-acetyl-p-aminophenol (APAP)-induced HepG2 cell ...

Journal: :Chemical communications 2011
Wen-Xiu Ni Wai-Lun Man Myra Ting-Wai Cheung Raymond Wai-Yin Sun Yuan-Lan Shu Yun-Wah Lam Chi-Ming Che Tai-Chu Lau

A nitridoosmium(VI) complex [Os(VI)(N)(sap)(OH(2))Cl] (H(2)sap = N-salicylidene-2-aminophenol) displays prominent in vitro and in vivo anti-cancer properties, induces S- and G2/M-phase arrest and forms a stable adduct with dianionic 5'-guanosine monophosphate.

Journal: :Dalton transactions 2012
Mohammad Mahdi Najafpour Mahmoud Amouzadeh Tabrizi Behzad Haghighi Govindjee

We describe here the ability of manganese oxide monosheets to aggregate to form layered structures with 4-aminophenol molecules. These aggregated monosheets could be considered as the first step to synthesize a self-assembled layered hybrid of phenol-manganese ions with phenol and manganese(III) and (IV) as exists in the water oxidizing complex of Photosystem II.

Journal: :Chemical communications 2014
Jia Wang Hongyang Liu Xianmo Gu Haihua Wang Dang Sheng Su

Nitrogen-containing ordered mesoporous carbon (NOMC) was synthesized by using m-aminophenol (MAP) as a carbon and nitrogen co-precursor via a co-assembly process with F127 in aqueous phase and exhibited a good catalytic performance for selective oxidation of ethylbenzene.

Journal: :Chemical communications 2015
Huawen Hu Xiaowen Wang Dagang Miao Yuanfeng Wang Chuilin Lai Yujuan Guo Wenyi Wang John H Xin Hong Hu

Using alkaline pH adjustment, the reaction between graphene oxide and L-ascorbic acid led to the formation of a carbocatalyst film with numerous graphene edges protruding out of basal planes, which had a markedly enhanced carbocatalytic activity for conversion of 4-nitrophenol to 4-aminophenol, as compared to that of the carbocatalyst counterpart without involving pH mediation.

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