| Weight | 697.778 g/mol |
|---|---|
| Formula | C37H47NO12 |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 6 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Rifamycin SV (15105-92-7, 6998-60-3)
Rifocyna · Rifamicina Colirio · Otafa
Score:
#476 in Microbiology
,
#1680 in Biochemistry
,
#3764 in Biology
,
#4740 in Chemistry
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- Interactions of rifamycin SV and rifampicin with organic anion uptake systems of human liver (Hepatology, 2002)
- Enantiomeric resolution using the macrocyclic antibiotics rifamycin B and rifamycin SV as chiral selectors for capillary electrophoresis (Journal of Chromatography A, 1995)
- Rifamycin SV and rifampicin exhibit differential inhibition of the hepatic rat organic anion transporting polypeptides, Oatp1 and Oatp2 (Hepatology, 2000)
- Complete genome sequence of the rifamycin SV-producing Amycolatopsis mediterranei U32 revealed its genetic characteristics in phylogeny and metabolism (Cell Research, 2010)
- Oxygen radical damage to DNA by rifamycin SV and copper ions. (Biochemical Pharmacology, 1987)
- The effect of an intravenous infusion of rifamycin SV on the excretion of bilirubin, bromsulphalein, and indocyanine green in man. (Gastroenterology, 1965)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Rifocyna
- Rifamicina Colirio
- Otafa
- rifamycin SV, sodium salt
- Rifocina
- Rifamycine Chibret
- Rifacin
- 5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-2,7-(epoxypentadeca(1,11,13)trienimino)naphtho(2,1-b)furan-1,11(2-H)-dione, 21-acetate
- rifamycin SV, monosodium salt
- R-75-1
-
SMILESCC1C=CC=C(C(=O)NC2=CC(=C3C(=C2O)C(=C(C4=C3C(=O)C(O4)(OC=CC(C(C(C(C(C(C1O)C)O)C)OC(=O)C)C)OC)C)C)O)O)C
-
InChIKeyHJYYPODYNSCCOU-UHFFFAOYSA-N
- Pubchem - Rifamycin SV
- Wikipedia - rifamycin
The rifamycins are a group of antibiotics that are synthesized either naturally by the bacterium Amycolatopsis rifamycinica or artificially. They are a subclass of the larger family of ansamycins. Rifamycins are particularly effective against mycobacteria, and are therefore used to treat tuberculosis, leprosy, and mycobacterium avium complex (MAC) infections.
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