scholarly journals Correlation between the structure and biological activity of some coordination compounds of isatin Schiff bases

2003 ◽  
Vol 57 (10) ◽  
pp. 444-448 ◽  
Author(s):  
Blaga Radovanovic ◽  
Sandra Konstantinovic
Keyword(s):  
Antimicrobial Activity ◽  
Biological Activity ◽  
Transition Metal ◽  
Schiff Bases ◽  
1H Nmr ◽  
Elemental Analysis ◽  
Coordination Compounds ◽  
Molar Conductivity ◽  
Enhanced Activity

The complexes of Co(ll), Ni(ll), Cu(ll) and Zn(ll) with isatin Schiff bases were synthetised and their structures established by using elemental analysis, as well as by measuring the molar conductivity, AA, FTIR, UV/VIS and 1H NMR and applying TG analysis.Isatin Schiff bases show different antimicrobial activity due to the different nature of the carbonyl and amino components as well as its substituent. The complexes have an enhanced activity compared to the ligands due to the transition metal involved in the coordination. It is also evident that the complexes have different antimicrobial activity, which is related to the nature and typeof coordinated metal.

Synthesis, characterization, and biological activities of some transition metal(II) complexes with the thiosemicarbazone derived from 4-[1-(4-methylphenylsulfonyl)-1H-indol-3-yl]but-3-en-2-one

2006 ◽  
Vol 60 (3) ◽  
Author(s):  
J. Qu ◽  
G. Sun ◽  
L. Wang ◽  
L. Qu
Keyword(s):  
Biological Activity ◽  
Transition Metal ◽  
General Formula ◽  
1H Nmr ◽  
Elemental Analysis ◽  
Nmr Spectra ◽  
Biological Activities ◽  
Antitumour Activity ◽  
Molar Conductivity

AbstractA new 4-[1-(4-methylphenylsulfonyl)-1H-indol-3-yl]but-3-en-2-one thiosemicarbazone (HL) was synthesized derived from 4-[1-(4-methylphenylsulfonyl)-1H-indol-3-yl]but-3-en-2-one. Four transition metal(II) complexes of HL have been prepared. Elemental analysis, molar conductivity, IR, UV, 1H NMR spectra, and TG-DTA have been used to characterize these complexes. The complexes have the general formula ML2, where M = Zn, Cu, Co, and Ni. The ligand and its complexes have been studied for their possible biological activity including anti-inflammatory, antibacterial, and antitumour activity in vitro.

SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL EVALUATION OF NOVEL S-SUBSTITUTED PHENACYL-1, 3, 4-TRIAZOLE-THIOL DERIVATIVES FOR ANTIMICROBIAL STUDIES

INDIAN DRUGS ◽  
2012 ◽  
Vol 49 (08) ◽  
pp. 14-20
Author(s):  
S. S Kerur ◽  
◽  
K. R Alagawadi ◽  
H. Zhu ◽  
F. V Manvi
Keyword(s):  
Antimicrobial Activity ◽  
Antibacterial Activity ◽  
Biological Activity ◽  
1H Nmr ◽  
Elemental Analysis ◽  
Biological Evaluation ◽  
Triazole Derivatives ◽  
Antimicrobial Studies

In the present study, synthesis and antimicrobial activity of 2,5-disubstituted triazole derivatives 5a-f are described. The structures of the newly synthesized compounds were confirmed by FTIR, 1H NMR, mass and elemental analysis. All compounds were screened for antitubercular and antibacterial activity. The results revealed that most of the compounds showed high or moderate biological activity against tested microorganisms.

Synthesis and Biological Evaluation of Various New Substituted 1,3,4-oxadiazole-2-thiols

2008 ◽  
Vol 59 (4) ◽  
Author(s):  
Gabriela Laura Almajan ◽  
Stefania Felicia Barbuceanu ◽  
Ioana Saramet ◽  
Mihaela Dinu ◽  
Cristian Vasile Doicin ◽  
...  
Keyword(s):  
Biological Activity ◽  
Plant Growth ◽  
1H Nmr ◽  
Elemental Analysis ◽  
13C Nmr ◽  
Biological Evaluation ◽  
Ethyl Chloroacetate ◽  
Low Concentrations ◽  
Synthesis And Biological Evaluation

5-[4-(4X-phenylsulfonyl)phenyl]-1,3,4-oxadiazole-2-thiols, X=H, Cl, Br, reacted with ethyl chloroacetate to give S-alkylated compounds. Aminomethylation of the thione form of oxadiazoles yielded N(3)-derivatives. All the products have been characterized by elemental analysis, IR, 1H-NMR and 13C-NMR. The plant-growth regulating effects of the title compounds were examined. From the biological activity results, we found that most compounds showed weak stimulatory activities at low concentrations.

scholarly journals Synthesis, Characterization and Study of the Biological activity of Some Aldimines Derivatives

2006 ◽  
Vol 3 (4) ◽  
pp. 257-261 ◽  
Author(s):  
Mohamed N. Ibrahim ◽  
Hazem K. Al - Deeb
Keyword(s):  
Biological Activity ◽  
Schiff Bases ◽  
Aromatic Aldehyde ◽  
Aromatic Amine ◽  
Elemental Analysis ◽  
Primary Aromatic Amine ◽  
H Nmr

A number of imines derivatives have been synthesized, they were obtained by condensation of aromatic aldehyde derivatives with primary aromatic amine derivatives. Their structures have been characterised by IR,1H NMR in addition to the elemental analysis. The biological activity of these imines (which are also known as Schiff bases) were examined against different type of microorganisms and they found to have considerable activity in comparison with the most commonly used antibiotics.

scholarly journals Characterization and biological evaluation of some novel pyrazolo[3',4':4,5]thieno[2,3-d]pyrimidin-8-ones synthesized via the Gewald reaction

2008 ◽  
Vol 73 (7) ◽  
pp. 683-690 ◽  
Author(s):  
Dipti Dodiya ◽  
Amit Trivedi ◽  
Samir Jarsania ◽  
Shailesh Vaghasia ◽  
Viresh Shah
Keyword(s):  
Antimicrobial Activity ◽  
1H Nmr ◽  
Elemental Analysis ◽  
13C Nmr ◽  
Spectroscopic Investigation ◽  
Aromatic Aldehydes ◽  
Biological Evaluation ◽  
Bacterial Strains ◽  
Gewald Reaction ◽  
Compound Ii

The synthesis of substituted pyrazolo[3',4':4,5]thieno[2,3-d]pyrimidin-8-ones (IIIa-j) from 5-amino-3-methyl-1H-thieno[3,2-c]pyrazole-6-carbonitrile (II) is described. The key compound II was synthesized from (5-methyl- -2,4-dihydro-3H-pyrazol-3-ylidene)malononitrile I via the Gewald reaction. The synthesis of the title compounds IIIa-j was accomplished by condensation of II with different aromatic aldehydes. The newly synthesized heterocyles were characterized by elemental analysis, IR, 1H-NMR, 13C-NMR and mass spectroscopic investigation. All the newly synthesized compounds were evaluated for antimicrobial activity against a variety of bacterial strains. .

Synthesis of New Phenoxypropylamines and Evaluation of their Antiulcer Activity as H2 -Receptor Antagonist

2012 ◽  
Vol 554-556 ◽  
pp. 1849-1852
Author(s):  
Hui Zhang ◽  
Min Fan Wu ◽  
Yu Tian ◽  
Jian Tong ◽  
Li Hong Shang
Keyword(s):  
Biological Activity ◽  
Receptor Antagonist ◽  
Gastric Acid ◽  
1H Nmr ◽  
Elemental Analysis ◽  
Antiulcer Activity ◽  
Antisecretory Activity ◽  
C Nmr

More new phenoxypropylamines have been synthesized. All the products have been characterized by elemental analysis, 1H-NMR, 1C-NMR and MS. The biological activity effects of the title compounds were examined. From the biological activity reSuperscript textsults, we found that some of them showed significant gastric acid antisecretory activity.

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