| Weight | 454.477 g/mol |
|---|---|
| Formula | C17H34N4O10 |
| Hydrogen Acceptors | 14 |
| Hydrogen Donors | 10 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
ribostamycin (25546-65-0)
SF-733 · SF 733 · SF733
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- Studies on antibiotic SF-733. A new antibiotic. II. Chemical structure of antibiotic SF-733. (The Journal of Antibiotics, 1970)
- Comparative Ototoxicity of Ribostamycin, Dactimicin, Dibekacin, Kanamycin, Amikacin, Tobramycin, Gentamicin, Sisomicin and Netilmicin in the Inner Ear of Guinea Pigs (Chemotherapy, 1990)
- 13C-NMR STUDIES ON RIBOSTAMYCIN AND ITS RELATED COMPOUNDS (The Journal of Antibiotics, 1973)
- The ribostamycin biosynthetic gene cluster in Streptomyces ribosidificus: comparison with butirosin biosynthesis. (Molecules and Cells, 2005)
- Stereochemistry of ribostamycin biosynthesis. Application of hydrogen-2 NMR spectroscopy (Journal of the American Chemical Society, 1981)
- RIBOSTAMYCIN, AS AN INTERMEDIATE IN THE BIOSYNTHESIS OF NEOMYCIN (The Journal of Antibiotics, 1977)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - SF-733
- SF 733
- SF733
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SMILESC1C(C(C(C(C1N)OC2C(C(C(C(O2)CN)O)O)N)OC3C(C(C(O3)CO)O)O)O)N
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InChIKeyNSKGQURZWSPSBC-UHFFFAOYSA-N
- Pubchem - ribostamycin
- Wikipedia - Ribostamycin
Ribostamycin is an aminoglycoside-aminocyclitol antibiotic isolated from a streptomycete, Streptomyces ribosidificus, originally identified in a soil sample from Tsu City of Mie Prefecture in Japan. It is made up of 3 ring subunits: 2-deoxystreptamine (DOS), neosamine C, and ribose. Ribostamycin, along with other aminoglycosides with the DOS subunit, is an important broad-spectrum antibiotic with important use against human immunodeficiency virus and is considered a critically important antimicrobial by the World Health Organization., Resistance against aminoglycoside antibiotics, such as ribostamycin, is a growing concern.
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