نتایج جستجو برای: inhibitory concentration 50

تعداد نتایج: 882418  

Journal: :Biochemical and biophysical research communications 2004
Byung-Moon Kim Hana Kim Ronald T Raines Younghoon Lee

Onconase (ONC) is currently in Phase III clinical trials as a cancer chemotherapeutic agent. Despite the finding that ONC contains an N-linked glycosylation site (-N69-V70-T71-), only the non-glycosylated form of the protein has been identified to date. We employed the Pichia pastoris expression system to produce recombinant glycosylated ONC (gONC) protein. Approximately 10 mg of ONC protein wa...

Journal: :ChemMedChem 2013
Roberta Ettari Lucia Tamborini Ilenia C Angelo Silvana Grasso Tanja Schirmeister Leonardo Lo Presti Carlo De Micheli Andrea Pinto Paola Conti

Novel rhodesain inhibitors were obtained by combining an enantiomerically pure 3-bromoisoxazoline warhead with a specific peptidomimetic recognition moiety. All derivatives behaved as inhibitors of rhodesain, with low micromolar Ki values. Their activity against the enzyme was found to be paralleled by an in vitro antitrypanosomal activity, with IC50 values in the mid-micromolar range. Notably,...

2016
Sun-Myoung Lee Hae-Yoon Kwon Jae-Hyoung Im Ji Hyeon Baek Seung-Sik Hwang Jae-Seung Kang Moon-Hyun Chung Jin-Soo Lee

Scrub typhus is a zoonosis caused by Orientia tsutsugamushi (O. tsutsugamushi) occurring mainly in autumn in Korea. The need of new antibiotics has arisen with a report on strains resistant to antibiotics and chronic infection. This study aims to identify susceptibility of tigecycline in-vitro as a new therapeutic option for O. tsutsugamushi. Antibacterial activity of tigecycline against the O....

Journal: :FEBS letters 2001
S K Singh K Maithal H Balaram P Balaram

Synthetic peptides corresponding to two distinct segments of the subunit interface of the homodimeric enzyme triosephosphate isomerase (residues 9-18, ANWKCNGTLE, peptide I; residues 68-79, KFGNGSYTGEVS, peptide II) from Plasmodium falciparum (PfTIM) have been investigated for their ability to act as inhibitors by interfering with the quaternary structure of the enzyme. An analog of peptide II ...

Journal: :ChemMedChem 2014
Soo-Kyung Kim William A Goddard Kyu Yang Yi Byung Ho Lee Chae Jo Lim Bartosz Trzaskowski

Human Urotensin-II (U-II) is the most potent mammalian vasoconstrictor known.1 Thus, a U-II antagonist would be of therapeutic value in a number of cardiovascular disorders.2 Here, we describe our work on the prediction of the structure of the human U-II receptor (hUT2 R) using GEnSeMBLE (GPCR Ensemble of Structures in Membrane BiLayer Environment) complete sampling Monte Carlo method. With the...

Journal: :Molecules 2017
Adriana Grozav Ioan-Dan Porumb Luiza Ioana Găină Lorena Filip Daniela Hanganu

Newly synthesized 2-(2-((1H-indol-5yl)methylene)-hydrazinyl)-thiazole derivatives were evaluated for their in vitro cytotoxicity on two carcinoma cell lines A2780 and HeLa. Significant cytotoxic activity for 2-(2-((1H-indol-5-yl)methylene)hydrazinyl)-4-methylthiazole (1) and 2-(2-((1H-indol-5-yl)methylene)hydrazinyl)-4-phenylthiazole (3), on both A2780 [IC50: 11.6 μM (1), and 12.4 μM (3)] and H...

Journal: :Molecules 2017
Xiaolin Song Hao Wu Zhenhao Yin Meilan Lian Chengri Yin

Ginsenoside is the most important secondary metabolite of ginseng. Natural sources of wild ginseng have been overexploited. Although root culture could reduce the length of the growth cycle of ginseng, the number of ginsenosides is fewer and their contents are lower in adventitious roots of ginseng than that in ginseng cultivated in the field. In this study, we investigated the effects of endop...

Journal: :Molecular biology of the cell 1993
J E Minor R J Britten E H Davidson

The sperm protein bindin is responsible for the species-specific adhesion of the sperm to the egg. The regions of the bindin molecule responsible for forming the contact between the sperm and the egg were investigated by measuring the ability of peptides representing various regions of the bindin sequence to inhibit fertilization. Twenty-four peptides were studied: 7 based on the Strongylocentr...

2016
Yong-Feng Chen Wen-Wen Jiang Shi-Qi Zhang Jian-Quan Kan Yong Liang

[This retracts the article DOI: 10.1155/2016/3537193.].

2013
Maizatul Akmal Yahayu Mawardi Rahmani Najihah Mohd Hashim Cheng Lian Ee Mohd Aspollah Sukari Abdah Md Akim

Phytochemical and biological studies were carried out the stem bark of Cratoxylum arborescens collected from Sarawak, Malaysia. Chromatographic separation of the plant extracts led to the isolation of three xanthones, -mangostin (1), -mangostin (2) and fuscaxanthone C (3) together with the commom stigmasterol. The structural elucidation of the compound was determined by detail spectroscopic a...

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