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1 erculosis antibiotic isoniazid (isonicotinic acid hydrazide).
2 evel of radicals was produced from nicotinic acid hydrazide.
3 carbonyl products with 3-hydroxy-2-naphthoic acid hydrazide.
4 n-bonding template composed of 5-aminoanisic 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
8 s, we screened a series of 71 arylcarboxylic acid hydrazide derivatives for their ability to induce m
9 erculosis antibiotic isoniazid (isonicotinic acid hydrazide), have confirmed that the heme iron in th
10 le myeloperoxidase inhibitor 4-amino-benzoic acid hydrazide, indicating peroxidase catalytic activity
11 tion of the antitubercular drug isonicotinic acid hydrazide (INH) and is important for survival of M.
12 ont-line antituberculosis agent isonicotinic acid hydrazide (INH) compared with the parental furA+ st
17 The standard method for preparing carboxylic acid hydrazides is hydrazinolysis of esters in alcoholic
18 r, a chemical inhibitor of MPO (aminobenzoic acid hydrazide) mimicked the effects of hLF1-11 on the i
19 eyes were reacted with 3-hydroxy-2-naphthoic acid hydrazide (NAH), and NAH-carbonyl compounds were de
21 f crude lysates revealed para-hydroxybenzoic acid hydrazide (pHBH) to be best suited for application
22 e less potent antitubercular agent nicotinic acid hydrazide produced the corresponding nicotinyl radi
24 onfers increased sensitivity to isonicotinic acid hydrazide, suggesting that the natural loss of oxyR
25 incubated with methimazole or 4-aminobenzoic acid hydrazide, which are inhibitors of myeloperoxidase,
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