Weight | 124.099 g/mol |
---|---|
Formula | C5H4N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Pyrazine-2-carboxylic acid (98-97-5)
pyrazinoic acid · pyrazinoate
Score:
#501 in Microbiology
,
#3973 in Biology
,
#5002 in Chemistry
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- Mode of action of pyrazinamide: disruption of Mycobacterium tuberculosis membrane transport and energetics by pyrazinoic acid (Journal of Antimicrobial Chemotherapy, 2003)
- Role of Acid pH and Deficient Efflux of Pyrazinoic Acid in Unique Susceptibility of Mycobacterium tuberculosis to Pyrazinamide (Journal of Bacteriology, 1999)
- Efficient H2O2 Oxidation of Alkanes and Arenes to Alkyl Peroxides and Phenols Catalyzed by the System Vanadate-Pyrazine-2-Carboxylic Acid (Journal of Catalysis, 1993)
- Mechanism of oxidations with H2O2 catalyzed by vanadate anion or oxovanadium(V) triethanolaminate (vanadatrane) in combination with pyrazine-2-carboxylic acid (PCA): Kinetic and DFT studies (Journal of Catalysis, 2009)
- Oxidation of 2-Propanol and Cyclohexane by the Reagent "Hydrogen Peroxide -Vanadate Anion-Pyrazine-2-carboxylic Acid": Kinetics and Mechanism (Journal of Physical Chemistry A, 2007)
- Effect of pyrazinamide and pyrazinoic acid on urate clearance and other discrete renal functions. (Experimental Biology and Medicine, 1957)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - pyrazinoic acid
- pyrazinoate
-
SMILESC1=CN=C(C=N1)C(=O)O
-
InChIKeyNIPZZXUFJPQHNH-UHFFFAOYSA-N
- Pubchem - Pyrazine-2-carboxylic acid
- Wikipedia - pyrazinoic acid
Pyrazinoic acid is a pyrazinamide metabolite.
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Similar Compounds
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ZX-CM014952
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methyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate
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