Weight | 123.115 g/mol |
---|---|
Formula | C5H5N3O |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Pyrazinamide (98-96-4)
Tisamid
Score:
#92 in Microbiology
,
#1085 in Biology
,
#1220 in Chemistry
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- Mutations in pncA, a gene encoding pyrazinamidase/nicotinamidase, cause resistance to the antituberculous drug pyrazinamide in tubercle bacillus. (Nature Medicine, 1996)
- The curious characteristics of pyrazinamide: a review. (International Journal of Tuberculosis and Lung Disease, 2003)
- Pyrazinamide Inhibits Trans-Translation in Mycobacterium tuberculosis (Science, 2011)
- Mode of action of pyrazinamide: disruption of Mycobacterium tuberculosis membrane transport and energetics by pyrazinoic acid (Journal of Antimicrobial Chemotherapy, 2003)
- 14-day bactericidal activity of PA-824, bedaquiline, pyrazinamide, and moxifloxacin combinations: a randomised trial (The Lancet, 2012)
- Rifampin and Pyrazinamide vs Isoniazid for Prevention of Tuberculosis in HIV-Infected Persons: An International Randomized Trial (JAMA, 2000)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Tisamid
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SMILESC1=CN=C(C=N1)C(=O)N
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InChIKeyIPEHBUMCGVEMRF-UHFFFAOYSA-N
- Pubchem - Pyrazinamide
- Wikipedia - pyrazinamide
Pyrazinamide is a medication used to treat tuberculosis. For active tuberculosis it is often used together with rifampin, isoniazid, and either streptomycin or ethambutol. It is not generally recommended for the treatment of latent tuberculosis.
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