Weight | 837.058 g/mol |
---|---|
Formula | C41H76N2O15 |
Hydrogen Acceptors | 17 |
Hydrogen Donors | 5 |
Aromatic Rings | 0 |
Rotatable Bonds | 13 |
roxithromycin (80214-83-1)
Score:
#400 in Microbiology
,
#3124 in Biology
,
#3907 in Chemistry
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- Randomised trial of roxithromycin in non-Q-wave coronary syndromes: ROXIS pilot study (The Lancet, 1997)
- Treatment with the antibiotic roxithromycin in patients with acute non-Q-wave coronary syndromes. The final report of the ROXIS study (European Heart Journal, 1999)
- Trial of roxithromycin in subjects with asthma and serological evidence of infection with Chlamydia pneumoniae (American Journal of Respiratory and Critical Care Medicine, 2001)
- Roxithromycin. A review of its antibacterial activity, pharmacokinetic properties and clinical efficacy. (Drugs, 1989)
- Randomized double-blind controlled trial of roxithromycin for prevention of abdominal aortic aneurysm expansion (British Journal of Surgery, 2001)
- Treatment of Chlamydia pneumoniae infection with roxithromycin and effect on neointima proliferation after coronary stent placement (ISAR-3): a randomised, double-blind, placebo-controlled trial (The Lancet, 2001)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC1C(C(C(C(=NOCOCCOC)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O
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- Pubchem - roxithromycin
- Wikipedia - roxithromycin
Roxithromycin is a semi-synthetic macrolide antibiotic. It is used to treat respiratory tract, urinary and soft tissue infections. Roxithromycin is derived from erythromycin, containing the same 14-membered lactone ring.
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