Results 131 to 140 of about 11,110 (180)
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Antimycobacterial Natural Products
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
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Heterocyclic Isosters of Antimycobacterial Salicylanilides.
ChemInform, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
Josef, Matyk +6 more
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Antimycobacterial and Antifungal Isosters of Salicylamides.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Karel, Waisser +9 more
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Antimycobacterial thiobenzanilides
Collection of Czechoslovak Chemical Communications, 1990A group of 30 thiobenzanilides active against Mycobacterium kansasii have been synthesized and their 1H NMR and UV spectra and RM values (TLC on silica gel impregnated with methylsilicone oil) have been measured. From the correlation between the chemical shifts of the thioamide proton in the 1H NMR spectra and the Hammett constants it can be concluded ...
Karel Waisser +5 more
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New Agents with Antimycobacterial Activity
Archiv der Pharmazie, 2005AbstractIn this paper, we report that a series of structurally simple a‐halogenoacetamides (1–8) show potent and excellent antimycobacterial activities against drug‐sensitive Mycobacterium tuberculosis H37Rv and drug‐resistant M. avium.
José, Marco-Contelles +1 more
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Pharmacology of the antimycobacterial drugs
Medical Clinics of North America, 1993The management of MDR-TB requires that the clinician become familiar with the "second-line" antimycobacterial agents. These drugs are generally less potent and frequently more toxic than isoniazid and rifampin. Because they are less active, innovative dosing schedules may allow us to take advantage of the few strengths that they possess.
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New antimycobacterialS-alkylisothiosemicarbazones
Folia Microbiologica, 2005In connection with a systematic study of antimycobacterial agents against potentially pathogenic strains the series of 12 S-alkylisothiosemicarbazones was evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis, M. kansasii, M. fortuitum, two strains of M. intracellulare and three strains of M. avium.
K, Waisser +3 more
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2001
Compounds represented by the formula [1] ##STR1## R.sub.1 is H or a substituent; R.sub.2 and R.sub.3 are C.sub.1 -C.sub.3 alkyl; R.sub.4 is siderophore group e.g. CH.sub.3 --(CH.sub.2).sub.n --C(O)--N(OH)--(CH.sub.2).sub.m -- with n=10-22, m=2-6; X is O, S, or NH; X.sub.1 is O or NH; Y is H or alkyl; Z is H or substituted amino, e.g., t-BocNH or CbzNH,
MILLER MARVIN J, XU YANPING
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Compounds represented by the formula [1] ##STR1## R.sub.1 is H or a substituent; R.sub.2 and R.sub.3 are C.sub.1 -C.sub.3 alkyl; R.sub.4 is siderophore group e.g. CH.sub.3 --(CH.sub.2).sub.n --C(O)--N(OH)--(CH.sub.2).sub.m -- with n=10-22, m=2-6; X is O, S, or NH; X.sub.1 is O or NH; Y is H or alkyl; Z is H or substituted amino, e.g., t-BocNH or CbzNH,
MILLER MARVIN J, XU YANPING
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1998
Abstract Antimycobacterial agents embrace a wide array of drug classes and are used to treat a host of infections. These infections include tuberculosis, the disease caused by Mycobacterium tuberculosis (MTB); leprosy, the disease caused by M.
Charles A Peloquin, Michael D Iseman
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Abstract Antimycobacterial agents embrace a wide array of drug classes and are used to treat a host of infections. These infections include tuberculosis, the disease caused by Mycobacterium tuberculosis (MTB); leprosy, the disease caused by M.
Charles A Peloquin, Michael D Iseman
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Antimycobacterial activity of diphenylpyraline derivatives
European Journal of Medicinal Chemistry, 20082-Substituted derivatives of diphenylpyraline and their 1-phenyl and 1-phenethyl analogues have been prepared in several steps from dihydropyridine-2(1H)-thiones. The structures of all new compounds have been confirmed by NMR spectroscopy. Their activity against Mycobacterium tuberculosis H(37)Rv as well as their cytotoxicity against human cells (HEK ...
Robert, Weis +6 more
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