نتایج جستجو برای: indole derivative

تعداد نتایج: 73834  

Journal: :Indian journal of physiology and pharmacology 1999
S Sarkar S Ghosh S Sengupta S Dasadhikari A Ghosh

The effect of prostaglandin (PG) inhibitors differing in their chemical nature, viz. Aspirin (acetylsalicylic acid), Mefenamic acid (fenamates), Diclofenac (phenylacetic acid derivative) and Piroxicam (oxicam derivative) on the adrenal hormones was studied in acutely stressed pigeons. None of these PG blockers exerted any significant effect on the catecholamine and corticosterone content of the...

Journal: :Journal of the American Chemical Society 2015
C Michael McGuirk Michael J Katz Charlotte L Stern Amy A Sarjeant Joseph T Hupp Omar K Farha Chad A Mirkin

Herein, we demonstrate that the incorporation of an acidic hydrogen-bond-donating squaramide moiety into a porous UiO-67 metal-organic framework (MOF) derivative leads to dramatic acceleration of the biorelevant Friedel-Crafts reaction between indole and β-nitrostyrene. In comparison, it is shown that free squaramide derivatives, not incorporated into MOF architectures, have no catalytic activi...

2011
Ana M. F. Oliveira-Campos Abdellatif M. Salaheldin Filipe A. Almeida Paz Ligia M. Rodrigues

The reaction of indole derivatives with cyanoacetic acid followed by treatment with DMFDMA gave the intermediate indolyl enaminonitriles (3). Further reaction with aminoguanidine yielded 5 ́-cyanomeridianin analogues (4). The same intermediate reacted with pmethoxyphenylhydrazine to give the pyrazolyl derivative (8). Treatment of (2E)-3-dimethylamino-2-(1H-indol-3-yl)-propenoate (3a) with hydrox...

Journal: :Chemistry Letters 2021

We developed iridium-catalyzed 2-position-selective C–H borylation of indole derivatives by modifying the structure a bipyridine-type ligand. The yields ranged from good to excellent, even on gram scale, and were dramatically improved addition urea derivative catalyst. introduced boryl group was converted chloro, bromo, phenyl groups without isolation borylated intermediate. Preliminary results...

Journal: :Vestnik Sankt-Peterburgskogo universiteta 2021

In our research performed using model of acoustic trauma at experimental animals (female hybrids F1 CBA and C57BL/6 lines) influence triazin-indole expression level hypoxia induced factor (HIF) in Corti’s organ was studied its therapy application. As a reference drug cytoflavin used. Investigated the form 1 % solution introduced into parenterally dosage 5, 7, 10 mg/kg with 2 hr intervals after ...

Journal: :European journal of medicinal chemistry 2011
Eduard Dolušić Pierre Larrieu Sébastien Blanc Frédéric Sapunaric Jenny Pouyez Laurence Moineaux Delphine Colette Vincent Stroobant Luc Pilotte Didier Colau Thierry Ferain Graeme Fraser Moreno Galleni Jean-Marie Frère Bernard Masereel Benoît Van den Eynde Johan Wouters Raphaël Frédérick

Indoleamine 2,3-dioxygenase (IDO) is an important new therapeutic target for the treatment of cancer. With the aim of discovering novel IDO inhibitors, a virtual screen was undertaken and led to the discovery of the keto-indole derivative 1a endowed with an inhibitory potency in the micromolar range. Detailed kinetics were performed and revealed an uncompetitive inhibition profile. Preliminary ...

Journal: :Molecules 2011
Cui-Cui Wang Hai-Zhou Liu Ming Liu Yu-Yan Zhang Tian-Tian Li Xiu-Kun Lin

A new polyketide compound 1 and a new naturally occurring chromone derivative 2, along with two known indole alkaloids 3-4 were characterized from the ethyl acetate extract of a soil-derived fungal strain, Exophiala pisciphila PHF-9. The structures of compounds 1-4 were established by detailed spectroscopic analysis and comparison with literature data. The absolute configuration of 1 was determ...

Journal: :Molecules 2018
Rania S Ali Hosam A Saad

Our current goal is the synthesis of polyheterocyclic compounds starting from 3-amino-[1,2,4]triazino[5,6-b]indole 1 and studying their anticancer activity to determine whether increasing of the size of the molecules increases the anticancer activity or not. 1-Amino[1,2,4]triazino[3',4':3,4]-[1,2,4]triazino[5,6-b]indole-2-carbonitrile (4) was prepared by the diazotization of 3-amino[1,2,4]-tria...

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