نتایج جستجو برای: indole derivatives

تعداد نتایج: 114196  

1997
Alexander V. Butin Vladimir T. Abaev Tat’yana A. Stroganova Andrey V. Gutnov

2-Nitroaryldifurylmethanes 1a and 1b, readily available by condensation of 2-nitrobenzaldehyde and 6-nitroveratraldehyde with 2-methylfuran, were transformed into indole, cinnoline and benzothiazine-3,1 derivatives. The reduction of 2-nitroaryldifurylmethanes gave the corresponding anilines 2a,b or indole 3 depending on the reaction conditions. A plausible mechanism for the last reaction involv...

Journal: :Journal of medicinal chemistry 2016
Andrea Unzue Hongtao Zhao Graziano Lolli Jing Dong Jian Zhu Melanie Zechner Aymeric Dolbois Amedeo Caflisch Cristina Nevado

Small-molecule hits for the bromodomains of CREBBP and BAZ2B have been identified by scaffold hopping followed by docking of a set of ∼200 compounds containing the acetyl indole scaffold. Chemical synthesis of nearly 30 derivatives has resulted in ligands of representatives of three subfamilies of human bromodomains with favorable ligand efficiency. The X-ray crystal structures of three differe...

Journal: :Bulletin of the Chemical Society of Japan 1967

Journal: :Bioorganic & medicinal chemistry 2013
Hernán Pessoa-Mahana Christian González-Lira Angélica Fierro Gerald Zapata-Torres C David Pessoa-Mahana Javiera Ortiz-Severin Patricio Iturriaga-Vásquez Miguel Reyes-Parada Paul Silva-Matus Claudio Saitz-Barría Ramiro Araya-Maturana

A series of 3-(3-(4-(3-(1H-indol-3-yl)propyl)piperazin-1-yl)propyl)-1H-indole derivatives (3a-d and 5a-f) as homo- and hetero-bis-ligands, were synthesized and evaluated for in vitro affinity at the serotonin transporter (SERT) and the 5-HT1A receptor. Compounds 5b and 5f showed nanomolar affinities for both targets. The experimental data were rationalized according to results obtained from doc...

Journal: :Chemical & pharmaceutical bulletin 2000
S Igarashi H Inami H Hara M Fujii H Koutoku H Oritani T Mase

In a search for novel nonsteroidal inhibitors of human prostatic 5alpha-reductase, we found a new series of indole derivatives that showed potent inhibitory activities for the human enzyme. Among them, 4-[(1-benzyl-1H-indol-5-yl)oxyl-3-chlorobenzoic acid (2d, YM-32906) showed more potent inhibitory activity than finasteride with an IC50 value of 0.44 nM. 3-Chloro-4-[[1-(4-phenoxybenzyl)-1H-indo...

2014
Kailin Han Haomeng Wang Binbin Song Yashan Li Wei Na Ding Hongye Zhao Hua Sun Yuou Teng Peng Yu

A series of novel 5-(2-Carboxyethenyl) indole derivatives were designed and synthesized about 38-48% overall yields. Two of the seven newly synthesized compounds, compound 5 and 7, have not been reported before. Their structures were characterized on the basis of H, C NMR, and those compounds were tested for their anticancer activities against K562 and HT-29 cell lines. Results indicated that c...

2011
Sujan Ganapathy

The indole nucleus seems to be a promising basis for design and synthesis of new derivatives able to protect oxidative stress in a variety of acute and chronic pathologies. The paper presents an overview of indole derived compounds in which inhibitory action has been demonstrated against potent microbes and also tested for antioxidant activity. Cellular damage caused by reactive oxygen species ...

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