Access the full text.
Sign up today, get DeepDyve free for 14 days.
A. Garedew, E. Schmolz, I. Lamprecht (2004)
Microcalorimetric investigation on the antimicrobial activity of honey of the stingless bee Trigona spp. and comparison of some parameters with those obtained with standard methodsThermochimica Acta, 415
H. Shrivastava, S. Devaraj, B. Nair (2004)
A Schiff base complex of chromium(III): an efficient inhibitor for the pathogenic and invasive potential of Shigella dysenteriae.Journal of inorganic biochemistry, 98 2
Chang-Li Xie, Tang Hou-Kuhan, Song Zhau-Hua, Song-Sheng Qu, Yao-Ting Liao, Hai-Shui Liu (1988)
Microcalorimetric study of bacterial growthThermochimica Acta, 123
A. Garedew, E. Schmolz, I. Lamprecht (2004)
Microbiological and calorimetric investigations on the antimicrobial actions of different propolis extracts: an in vitro approach ☆Thermochimica Acta, 422
A. Beezer, L. Ashby, S. Morais, R. Bolton, M. Shafiq, N. Kjeldsen (1990)
Drug bioassay, synergic interactions in drug combinations, thermodynamics and biologically based structure-activity relationships. A synthesisThermochimica Acta, 172
M. Hossain, Mohammad Alam, J. Begum, M. Ali, M. Nazimuddin, F. Smith, R. Hynes (1996)
The preparation, characterization, crystal structure and biological activities of some copper(II) complexes of the 2-benzoylpyridine Schiff bases of S-methyl- and S-benzyldithiocarbazateInorganica Chimica Acta, 249
Li-xia Zhang, Yi Liu, Li-Hua Cia, Yanxia Hu, Jun Yin, Peilei Hu (2006)
Inhibitory study of some novel Schiff base derivatives on Staphylococcus aureus by microcalorimetryThermochimica Acta, 440
L. Khoo, J. Charland, E. Gabe, F. Smith (1987)
Synthesis and structural studies for a series of aromatic Schiff base complexes with triphenyltin chloride and triphenyltin isothiocyanateInorganica Chimica Acta, 128
M. O'Neill, G. Vine, A. Beezer, A. Bishop, J. Hadgraft, C. Labetoulle, M. Walker, P. Bowler (2003)
Antimicrobial properties of silver-containing wound dressings: a microcalorimetric study.International journal of pharmaceutics, 263 1-2
Huang Zaiyin, L. Yi, Q. Songsheng, Feng Ying (1998)
A comparative study on half-inhibitory concentration of Schiff base-metal complexes reacting with bacteria
A. Soliman, W. Linert (1999)
Investigations on new transition metal chelates of the 3-methoxy-salicylidene-2-aminothiophenol Schiff baseThermochimica Acta, 338
Xi Li, Yi Liu, Jun Wu, S. Qu (2010)
Action of the Selenomorpholine Compounds on the Bacterium Growth by MicrocalorimetryChinese Journal of Chemistry, 20
J. Modi, S. Sabnis, C. Deliwala (1970)
Potential anticancer agents. 3. Schiff bases from benzaldehyde nitrogen mustards and aminophenylthiazoles.Journal of medicinal chemistry, 13 5
E. Hodnett, W. Dunn (1970)
Structure-antitumor activity correlation of some Schiff bases.Journal of medicinal chemistry, 13 4
M. Montanari, A. Andricopulo, C. Montanari (2004)
Calorimetry and structure–activity relationships for a series of antimicrobial hydrazidesThermochimica Acta, 417
F. Popp, S. Roth, J. Kirby (1963)
SYNTHESIS OF POTENTIAL ANTINEOPLASTIC AGENTS. IX. SOME CYCLOALKYL MUSTARDS AND RELATED COMPOUNDS.Journal of medicinal chemistry, 6
E. Hodnett, W. Dunn (1972)
Cobalt derivatives of Schiff bases of aliphatic amines as antitumor agents.Journal of medicinal chemistry, 15 3
Jun-cheng Zhu, Yi Liu, W. Wong, Bo Zhou, Jun Yin (2006)
Investigation of Antibacterial Activity of Two Kinds of Novel Schiff Bases on Escherichia coli by MicrocalorimetryChinese Journal of Chemistry, 24
Alexandra Torres, A. Garedew, E. Schmolz, I. Lamprecht (2004)
Calorimetric investigation of the antimicrobial action and insight into the chemical properties of “angelita” honey—a product of the stingless bee Tetragonisca angustula from ColombiaThermochimica Acta, 415
T. Aminabhavi, N. Biradar, S. Patil, V. Roddabasanagoudar, W. Rudzinski (1985)
Amino acid schiff base complexes of dimethyldichlorosilaneInorganica Chimica Acta, 107
T. Takeuchi, A. Boettcher, C. Quezada, T. Meade, H. Gray (1999)
Inhibition of thermolysin and human α-thrombin by cobalt(III) Schiff base complexesBioorganic & Medicinal Chemistry, 7
Xie Chang-li, Sun Day-Ung, Song Zhau-Hua, Q. Songsheng, Guo Yu, Li Bing (1992)
Microcalorimetric studies onTetrahymena pyriformis Part 2. Photosensitizer toxic effect onTetrahymena pyriformisThermochimica Acta, 197
J. Seydel, M. Wiese (2002)
Drug-membrane interactions : analysis, drug distribution, modeling
E. Schmolz, Fadimana Kösece, I. Lamprecht (2005)
Energetics of honeybee development: Isoperibol and combustion calorimetric investigationsThermochimica Acta, 437
B. Chowdhry, A. Beezer, E. Greenhow (1983)
Analysis of drugs by microcalorimetry Isothermal power-conduction calorimetry and thermometric titrimetry.Talanta, 30 4
K. Thimmaiah, W. Lloyd, G. Chandrappa (1985)
Stereochemistry and fungitoxicity of complexes of p-anisaldehydethiosemicarbazone with Mn(II), Fe(II), Co(II) and Ni(II)Inorganica Chimica Acta, 106
E. Kosower, T. Miyadera (1972)
Glutathione. 6. Probable mechanism of action of diazene antibiotics.Journal of medicinal chemistry, 15 3
The antibacterial effect of a series of novel pyridine amide Schiff base compounds on Escherichia coli was investigated by a microcalorimetric method at 37 °C. The metabolic power‐time curves of the bacteria treated by the compounds were obtained, and the thermokinetic parameters were analyzed, from which the antibacterial activities of these compounds were evaluated. The results show that two compounds F and G have good activity on aerobic multiplying metabolism of E. coli, with the value of IC50 106 and 113 mg/L respectively, but have no effective action on the fermentation metabolism of E. coli. The action of the compounds on the non‐multiplying metabolism was investigated by taking the heat output of E. coli in the stationary phase as the guideline of the activity. The experimental results revealed that the hydrophilicity of these Schiff bases had a great influence on their antibacterial activity, which results from the bacterial cell wall structure. The antibacterial structure‐activity relationship of these Schiff base derivatives was also briefly discussed. The antibacterial activity of the compounds against E. coli was as follows: compound F>G>C>D>E>B>A.
Chinese Journal of Chemistry – Wiley
Published: Sep 1, 2008
Keywords: ; ; ; ;
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.