نتایج جستجو برای: thiazole

تعداد نتایج: 1980  

2015
Rupert G D Taylor Joseph Cameron Iain A Wright Neil Thomson Olena Avramchenko Alexander L Kanibolotsky Anto R Inigo Tell Tuttle Peter J Skabara

Two novel tetrathiafulvalene (TTF) containing compounds 1 and 2 have been synthesised via a four-fold Stille coupling between a tetrabromo-dithienoTTF 5 and stannylated thiophene 6 or thiazole 4. The optical and electrochemical properties of compounds 1 and 2 have been measured by UV-vis spectroscopy and cyclic voltammetry and the results compared with density functional theory (DFT) calculatio...

2008
B. M. Gurupadayya M. Gopal B. Padmashali Y. N. Manohara

Various 7-chloro-6-fluoro-2-arylidenylaminobenzo(1,3)thiazole (2a-h) have been synthesized by the condensation of 7-chloro-6-fluoro-2-aminobenzo(1,3)thiazole (1) with different aromatic aldehydes. The Schiff's bases on reaction with acetyl chloride, chloroacetyl chloride and phenyl acetyl chloride yielded 1-(7-chloro-6-fluorobenzothiazol-2-yl)-3,4-substituted-aryl-azetidin-2-ones (3a-x). Simila...

Journal: :Cell chemical biology 2016
Luisa Quinti Malcolm Casale Sébastien Moniot Teresa F Pais Michael J Van Kanegan Linda S Kaltenbach Judit Pallos Ryan G Lim Sharadha Dayalan Naidu Heike Runne Lisa Meisel Nazifa Abdul Rauf Dmitriy Leyfer Michele M Maxwell Eddine Saiah John E Landers Ruth Luthi-Carter Ruben Abagyan Albena T Dinkova-Kostova Clemens Steegborn J Lawrence Marsh Donald C Lo Leslie M Thompson Aleksey G Kazantsev

There are currently no disease-modifying therapies for the neurodegenerative disorder Huntington's disease (HD). This study identified novel thiazole-containing inhibitors of the deacetylase sirtuin-2 (SIRT2) with neuroprotective activity in ex vivo brain slice and Drosophila models of HD. A systems biology approach revealed an additional SIRT2-independent property of the lead-compound, MIND4, ...

Journal: :The Journal of organic chemistry 2002
Teresa M V D Pinho e Melo Maria I L Soares António M d'A Rocha Gonsalves José A Paixão Ana M Beja Manuela Ramos Silva Luiz Alte da Veiga João Costa Pessoa

Intramolecular dipolar cycloaddition of bicyclic münchnones, 5H,7H-thiazolo[3,4-c]oxazol-4-ium-1-olates, derived from cyclodehydration of 2-substituted-N-acylthiazolidine-4-carboxylic acids are reported. A range of new pyrrolo[1,2-c]thiazole derivatives (7, 14, 15, 20, 23, and 26) were obtained as single enantiomers from 2-phenylthiazolidines, 2-benzoylthiazolidines, and 2-methylthiazolidine-4-...

2017
Leila Hosseinzadeh Alireza Aliabadi Mohsen Rahnama Hamid Mir Mohammad Sadeghi Marzieh Rahmani Khajouei

Quinazolinones are a group of heterocyclic compounds that have important biological activities such as cytotoxicity, anti-bacterial, and anti-fungal effects. Thiazole-containing compounds have also many biological effects including antitumor, antibacterial, anti-inflammatory, and analgesic activities. Due to significant cytotoxic effects of both quinazoline and thiazole derivatives, in this wor...

Journal: :Antimicrobial agents and chemotherapy 1977
M Dymicky C N Huhtanen A E Wasserman

A number of 5-nitrothiazoles with various substituents in the 2-position were tested for inhibition of Clostridium botulinum in a culture medium. Thiazole itself or 2-bromo- or 2-methylthiazole at 30 mug/ml did not inhibit the organism. An amino group in the 2-position of thiazole inhibited at 10 mug/ml. Substitution of a nitro group in the 5-position of 2-aminothiazole increased the inhibitory...

Journal: :Organic & biomolecular chemistry 2013
Panayiotis A Koutentis Maria Koyioni Sophia S Michaelidou

The thermolysis of several N-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)pyridin-n-amines (where n = 2, 3 and 4) gives a mixture of thiazolopyridine-2-carbonitriles in low to moderate yields. Introduction, by design, of a chlorine substituent at the C2 or C4 position of N-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)pyridin-3-amine and other selected azines enables a BnEt(3)NI mediated ANRORC style ring t...

Journal: :Dalton transactions 2009
Thomas Foerster Derek A Wann Heather E Robertson David W H Rankin

The structures of 1-trimethylsilyl-1,2,3-benzotriazole and 2-trimethylsilyl-1,3-thiazole have been determined by gas electron diffraction and computational methods. While 1-trimethylsilyl-1,2,3-benzotriazole shows a significant asymmetry in the way the SiMe(3) groups bonds to the ring system, the same is not true for 2-trimethylsilyl-1,3-thiazole. However, it has been shown that when the positi...

2015
Shiliang Li Guoqin Luan Xiaoli Ren Wenlin Song Liuxin Xu Minghao Xu Junsheng Zhu Dong Dong Yanyan Diao Xiaofeng Liu Lili Zhu Rui Wang Zhenjiang Zhao Yufang Xu Honglin Li

Human dihydroorotate dehydrogenase (hDHODH) is an attractive therapeutic target for the treatment of rheumatoid arthritis, transplant rejection and other autoimmune diseases. Based on the X-ray structure of hDHODH in complex with lead compound 7, a series of benzylidenehydrazinyl-substituted thiazole derivatives as potent inhibitors of hDHODH were designed and synthesized, of which 19 and 30 we...

Journal: :Acta pharmaceutica 2015
Lulzime Ballazhi Emil Popovski Ahmed Jashari Faik Imeri Ibrahim Ibrahimi Bozhana Mikhova Kristina Mladenovska

The study highlights the current progress in the development of coumarin scaffolds for drug discovery as novel anticancer agents in metastatic breast cancer. Eight compounds, combining the coumarin core and five membered heterocycles (isoxazoles and thiazoles) in hydrazinyldiene- -chroman-2,4-diones, were characterized in terms of a potential antiproliferative effect on bone (SCP1833) and lung ...

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