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1 erculosis antibiotic isoniazid (isonicotinic acid hydrazide).
2 n-bonding template composed of 5-aminoanisic acid hydrazide.
3 evel of radicals was produced from nicotinic acid hydrazide.
4 carbonyl products with 3-hydroxy-2-naphthoic acid hydrazide.
5 ddition, co-administration of 4-aminobenzoic acid hydrazide (4-ABAH), an irreversible inhibitor of MP
6 mice were treated with either 4-aminobenzoic acid hydrazide (ABAH), 40 mg/kg injected intraperitoneal
7                         The resultant adipic acid hydrazide derivatives (AH-proteins), containing 2.3
8 s, we screened a series of 71 arylcarboxylic acid hydrazide derivatives for their ability to induce m
9 semicarbazide (SEM) and 3,5-dinitrosalicylic acid hydrazide (DNSH).
10 erculosis antibiotic isoniazid (isonicotinic acid hydrazide), have confirmed that the heme iron in th
11                              An isonicotinic acid hydrazide (INAH) chemically modified fumed silica,
12 ophils with an MPO inhibitor (4-Aminobenzoic acid hydrazide) increased cell viability and delayed apo
13 le myeloperoxidase inhibitor 4-amino-benzoic acid hydrazide, indicating peroxidase catalytic activity
14 tion of the antitubercular drug isonicotinic acid hydrazide (INH) and is important for survival of M.
15 ont-line antituberculosis agent isonicotinic acid hydrazide (INH) compared with the parental furA+ st
16 f Mycobacterium tuberculosis to isonicotinic acid hydrazide (INH) lacks satisfactory definition.
17 nsitivity of M. tuberculosis to isonicotinic acid hydrazide (INH).
18 erculosis drug isoniazid [i.e., isonicotinic acid hydrazide (INH)].
19             Although isoniazid (isonicotinic acid hydrazide, INH) is widely used for the treatment of
20 The standard method for preparing carboxylic acid hydrazides is hydrazinolysis of esters in alcoholic
21 r, a chemical inhibitor of MPO (aminobenzoic acid hydrazide) mimicked the effects of hLF1-11 on the i
22 eyes were reacted with 3-hydroxy-2-naphthoic acid hydrazide (NAH), and NAH-carbonyl compounds were de
23                  Methimazole, 4-aminobenzoic acid hydrazide, or azide inhibits the reaction, suggesti
24 f crude lysates revealed para-hydroxybenzoic acid hydrazide (pHBH) to be best suited for application
25 e less potent antitubercular agent nicotinic acid hydrazide produced the corresponding nicotinyl radi
26             The MPO inhibitor 4-aminobenzoic acid hydrazide reduced peroxidase activity of neutrophil
27 onfers increased sensitivity to isonicotinic acid hydrazide, suggesting that the natural loss of oxyR
28  BCG growth inhibitor, 2-thiophenecarboxylic acid hydrazide (TCH), was used to prevent quantification
29 incubated with methimazole or 4-aminobenzoic acid hydrazide, which are inhibitors of myeloperoxidase,