Weight | 166.249 g/mol |
---|---|
Formula | C8H10N2S |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
ethionamide (536-33-4)
Trecator · Trecator SC · Ethioniamide
Score:
#149 in Microbiology
,
#489 in Biochemistry
,
#1556 in Biology
,
#1822 in Chemistry
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- inhA, A gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis (Science, 1994)
- Ethionamide activation and sensitivity in multidrug- resistant Mycobacterium tuberculosis (Proceedings of the National Academy of Sciences of the United States of America, 2000)
- Activation of the Pro-drug Ethionamide Is Regulated in Mycobacteria (Journal of Biological Chemistry, 2000)
- ethA, inhA, and katG Loci of Ethionamide-Resistant Clinical Mycobacterium tuberculosis Isolates (Antimicrobial Agents and Chemotherapy, 2003)
- Studies on the Mechanism of Action of Isoniazid and Ethionamide in the Chemotherapy of Tuberculosis (Journal of the American Chemical Society, 1995)
- Overexpression of inhA, but not kasA, confers resistance to isoniazid and ethionamide in Mycobacterium smegmatis, M. bovis BCG and M. tuberculosis. (Molecular Microbiology, 2002)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Trecator
- Trecator SC
- Ethioniamide
- Wyeth Brand of Ethionamide
- Amidazine
- Trecator-SC
-
SMILESCCC1=NC=CC(=C1)C(=S)N
-
InChIKeyAEOCXXJPGCBFJA-UHFFFAOYSA-N
- Pubchem - ethionamide
- Wikipedia - ethionamide
Ethionamide is an antibiotic used to treat tuberculosis. Specifically it is used, along with other antituberculosis medications, to treat active multidrug-resistant tuberculosis. It is no longer recommended for leprosy.
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