ISBN: 9786200277633 - synthesis of heterocycles and their biological evaluation: ultrasound-assisted synthesis of (bis)benzothiazole-pyrazolylpyrazolines and biological screening (9 risultati)

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Taschenbuch. Condizione: Neu. Synthesis of Heterocycles and Their Biological Evaluation | Ultrasound-Assisted Synthesis of (Bis)benzothiazole-pyrazolylpyrazolines and Biological Screening | Haresh B. Patel (u. a.) | Taschenbuch | 56 S. | Englisch | 2019 | LAP LAMBERT Academic Publishing | EAN 9786200277633 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -A new series of (bis)benzothiazole-pyrazolylpyrazoline derivatives were synthesized in one step by condensing suitably substituted chalcones, hydrazinobenzothiazoles and NaOH under ultrasonication method. All the newly synthesized compounds were screened for their antituberculosis and antimalarial activities. Among them, compounds 6a (MIC = 62.5 µg/mL), 6e (MIC = 25 µg/mL), 6f (MIC = 25 µg/mL), 6g (MIC = 12.5 µg/mL) and 6h (MIC = 12.5 µg/mL) were found to be good to excellent activity as compared to rifampicin (MIC = 40 µg/mL) against M. tuberculosis. In vitro activity against P. falciparum, compounds 6e (IC50 = 0.076 µg/mL), 6f (IC50 = 0.098 µg/mL) and 6g (IC50 = 0.085 µg/mL) exhibited the highest antimalarial activity and compounds 5e, 5g, 6a and 6h showed the good activity as compared to quinine (IC50 = 0.268 µg/mL). The brine shrimp bioassay was carried out to study the in vitro cytotoxic properties of the synthesized compounds. These results indicate that the synthesized compounds can leads to development of new potent member of antitubercular and antimalarial agents. This book is useful for researcher and Academia who are working in this field. 56 pp. Englisch.…

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Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - A new series of (bis)benzothiazole-pyrazolylpyrazoline derivatives were synthesized in one step by condensing suitably substituted chalcones, hydrazinobenzothiazoles and NaOH under ultrasonication method. All the newly synthesized compounds were screened for their antituberculosis and antimalarial activities. Among them, compounds 6a (MIC = 62.5 µg/mL), 6e (MIC = 25 µg/mL), 6f (MIC = 25 µg/mL), 6g (MIC = 12.5 µg/mL) and 6h (MIC = 12.5 µg/mL) were found to be good to excellent activity as compared to rifampicin (MIC = 40 µg/mL) against M. tuberculosis. In vitro activity against P. falciparum, compounds 6e (IC50 = 0.076 µg/mL), 6f (IC50 = 0.098 µg/mL) and 6g (IC50 = 0.085 µg/mL) exhibited the highest antimalarial activity and compounds 5e, 5g, 6a and 6h showed the good activity as compared to quinine (IC50 = 0.268 µg/mL). The brine shrimp bioassay was carried out to study the in vitro cytotoxic properties of the synthesized compounds. These results indicate that the synthesized compounds can leads to development of new potent member of antitubercular and antimalarial agents. This book is useful for researcher and Academia who are working in this field. …

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Patel Haresh B.Dr. Haresh has did his M.Sc. with specialization Analytical Chemistry and his Doctoral Study under Guidance of Dr. M. P. Patel Sir from S. P. University, V. V. Nagar. He has good command in synthesizing Drugs intermedi. …

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -A new series of (bis)benzothiazole-pyrazolylpyrazoline derivatives were synthesized in one step by condensing suitably substituted chalcones, hydrazinobenzothiazoles and NaOH under ultrasonication method. All the newly synthesized compounds were screened for their antituberculosis and antimalarial activities. Among them, compounds 6a (MIC = 62.5 µg/mL), 6e (MIC = 25 µg/mL), 6f (MIC = 25 µg/mL), 6g (MIC = 12.5 µg/mL) and 6h (MIC = 12.5 µg/mL) were found to be good to excellent activity as compared to rifampicin (MIC = 40 µg/mL) against M. tuberculosis. In vitro activity against P. falciparum, compounds 6e (IC50 = 0.076 µg/mL), 6f (IC50 = 0.098 µg/mL) and 6g (IC50 = 0.085 µg/mL) exhibited the highest antimalarial activity and compounds 5e, 5g, 6a and 6h showed the good activity as compared to quinine (IC50 = 0.268 µg/mL). The brine shrimp bioassay was carried out to study the in vitro cytotoxic properties of the synthesized compounds. These results indicate that the synthesized compounds can leads to development of new potent member of antitubercular and antimalarial agents. This book is useful for researcher and Academia who are working in this field.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 56 pp. Englisch. …