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1 than KatG(S315T) at converting isoniazid to isonicotinic acid.
2 ctionalized with the adsorbents catechol and isonicotinic acid.
3 gand, also increased PGD(2) release, whereas isonicotinic acid, a nicotinic acid analog with low affi
5 ovalent HYNIC conjugate 15 using tricine and isonicotinic acid as coligands with HYNIC for coordinati
6 ye moieties, isonicotinic acid (INA) and bis-isonicotinic acid (BINA), attached to TiO2 nanoparticles
7 L = 4-dimethylaminopyridine (dmap) and nic = isonicotinic acid, form hydrogen-bonded mixed-valence di
8 diphenyl-1,10-phenanthroline and 4-COOHPy is isonicotinic acid, has been evaluated for use in fluores
9 diphenyl-1,10-phenanthroline and 4-COOHPy is isonicotinic acid, has been synthesized and characterize
10 or the activation of the antitubercular drug isonicotinic acid hydrazide (INH) and is important for s
11 ive to the front-line antituberculosis agent isonicotinic acid hydrazide (INH) compared with the pare
12 sensitivity of Mycobacterium tuberculosis to isonicotinic acid hydrazide (INH) lacks satisfactory def
15 f the antituberculosis antibiotic isoniazid (isonicotinic acid hydrazide), have confirmed that the he
18 nactivation confers increased sensitivity to isonicotinic acid hydrazide, suggesting that the natural
19 possible dynamics of two small dye moieties, isonicotinic acid (INA) and bis-isonicotinic acid (BINA)
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