4329-75-3
Chemical Structure
N'-Isonicotinoylisonicotinohydrazide
Synonym(s): 1,2-Diisonicotinoylhydrazine
- CAS No.: 4329-75-3
- Formula:C12H10N4O2
- Molecular Weight:242.23
IUPAC Name: 2-amino-2-(naphthalen-2-yl)acetic acid hydrochloride
InChIKey: HDADCMZPLLONGB-UHFFFAOYSA-N
SMILES: O=C(C1=CC=NC=C1)NNC(C2=CC=NC=C2)=O
Biological Activity: N'-Isonicotinoylisonicotinohydrazide (Compound 7, 1,2-Diisonicotinoylhydrazine) is a competitive inhibitor (IC50=5-30 μM) of bacterial heme oxygenase (HO). N'-Isonicotinoylisonicotinohydrazide inhibits iron release and bacterial iron acquisition. N'-Isonicotinoylisonicotinohydrazide exhibits selective activity against HO enzymes from Pseudomonas aeruginosa and Neisseria meningitidis. N'-Isonicotinoylisonicotinohydrazide is promising for research of multidrug-resistant Gram-negative bacterial infections[1][2].
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N'-Isonicotinoylisonicotinohydrazide | N'-Isonicotinoylisonicotinohydrazide (Compound 7, 1,2-Diisonicotinoylhydrazine) is a competitive inhibitor (IC50=5-30 μM) of bacterial heme oxygenase (HO). N'-Isonicotinoylisonicotinohydrazide inhibits iron release and bacterial iron acquisition. N'-Isonicotinoylisonicotinohydrazide exhibits selective activity against HO enzymes from Pseudomonas aeruginosa and Neisseria meningitidis. N'-Isonicotinoylisonicotinohydrazide is promising for research of multidrug-resistant Gram-negative bacterial infections. | |||||||||||||||||||||
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- [1]. Furci LM, et al. Inhibition of the bacterial heme oxygenases from Pseudomonas aeruginosa and Neisseria meningitidis: novel antimicrobial targets. J Med Chem. 2007 Aug 9;50(16):3804-13. [Content Brief]
- [2]. Panda SS, et al. Synthesis, computational studies, antimycobacterial and antibacterial properties of pyrazinoic acid-isoniazid hybrid conjugates. RSC Adv. 2019 Jul 1;9(35):20450-20462. [Content Brief]
Keywords