| Weight | 822.953 g/mol |
|---|---|
| Formula | C43H58N4O12 |
| Hydrogen Acceptors | 15 |
| Hydrogen Donors | 6 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
Rifadin (13292-46-1, 62534-43-4)
Rifampin · Rifampicin · Rimactane
Score:
#14 in Microbiology
,
#435 in Biology
,
#451 in Chemistry
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- Rapid Molecular Detection of Tuberculosis and Rifampin Resistance (The New England Journal of Medicine, 2010)
- Detection of rifampicin-resistance mutations in Mycobacterium tuberculosis (The Lancet, 1993)
- Role of Rifampin for Treatment of Orthopedic Implant-Related Staphylococcal Infections A Randomized Controlled Trial (JAMA, 1998)
- The role of intestinal P-glycoprotein in the interaction of digoxin and rifampin. (Journal of Clinical Investigation, 1999)
- Nuclear Receptor Response Elements Mediate Induction of Intestinal MDR1 by Rifampin (Journal of Biological Chemistry, 2001)
- Structural Mechanism for Rifampicin Inhibition of Bacterial RNA Polymerase (Cell, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Rifampin
- Rifampicin
- Rimactane
- Rimactan
- Tubocin
- Benemycin
-
SMILESCC1C=CC=C(C(=O)NC2=C(C3=C(C(=C4C(=C3C(=O)C2=CNN5CCN(CC5)C)C(=O)C(O4)(OC=CC(C(C(C(C(C(C1O)C)O)C)OC(=O)C)C)OC)C)C)O)O)C
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