… resistance can also develop through alterations or overexpression of the INH drug target
InhA, and 0 to 5% of INH-resistant M. tuberculosis isolates have mutations in the inhA open …

… We also report ternary cocrystals of INH, INH·NA·SA and INH·NA·FA. All the solid forms
are thoroughly characterized by spectroscopic, X-ray diffraction and thermal techniques. In …

… for synthesis of INH-C16, INH-C17 and INH-C18 respectively, followed by … INH-C16,
INH-C17 and INH-C18 were chemically synthesized by augmenting the amine side chain of INH …

… anti‐tuberculosis agent isoniazid. However, most interestingly, no cross resistance was
observed between pyridomycin and isoniazid, … most frequently encountered isoniazid‐resistant …

… RMP-resistant TB, INH susceptibility may correlate with susceptibility to other antituberculosis
drugs, and this knowledge might help in planning more effective treatment regimens. Our …

… Isoniazid with different 5-substituted indole-3-carboxaldehyde. Thus, this study offers eco-friendly
and economical disposal of expired drug isoniazid … earlier studied isoniazid derivatives …

… This INH intermediate in the presence of NADH forms INH-NAD adduct which inhibits inhA
(… Isoniazid is used in conjunction with other effective anti-tuberculosis agents under multi-drug …

… Here, we investigated the reactivity of isoniazid metal complexes as prototypes for novel
self… isoniazid or (isoniazid)pentacyanoferrate(II) complex resulted in similar oxidized isoniazid …

… ppm, isoniazid derivatives with an MIC of 6.9 μM, and the N-(Disubstitutedbenzoyl)Isoniazid …
So, recently we have designed and computational study some isoniazid derivatives to be …

… isoniazid (INH) and the chemical structures of INH, cucurbiturils Q[6] and Q[7], acetyl coenzyme
A and acylating agents. … thioester groups that are used to convey the acetyl group to INH. …