Weight | 828.006 g/mol |
---|---|
Formula | C42H69NO15 |
Hydrogen Acceptors | 16 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 12 |
josamycin (16846-24-5)
EN 141 · Kitasamycin A3 · Leucomycin A3
Score:
#410 in Microbiology
,
#1338 in Biochemistry
,
#3255 in Biology
,
#4065 in Chemistry
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- Immunomodulatory effects of three macrolides, midecamycin acetate, josamycin, and clarithromycin, on human T-lymphocyte function in vitro. (Antimicrobial Agents and Chemotherapy, 1994)
- Formation of inactive cytochrome P-450 Fe(II)-metabolite complexes with several erythromycin derivatives but not with josamycin and midecamycin in rats (Biochemical Pharmacology, 1983)
- Kinetics of Macrolide Action THE JOSAMYCIN AND ERYTHROMYCIN CASES (Journal of Biological Chemistry, 2004)
- Randomized trial of doxycycline versus josamycin for Mediterranean spotted fever. (Antimicrobial Agents and Chemotherapy, 1990)
- Total synthesis of carbomycin B and josamycin (leucomycin A3) (Tetrahedron Letters, 1980)
- Clinical Efficacy and Tolerance of Two New Macrolides, Clarithromycin and Josamycin, in the Treatment of Patients with Acute Exacerbations of Chronic Bronchitis (Journal of International Medical Research, 1990)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - EN 141
- Kitasamycin A3
- Leucomycin A3
- EN141
- EN-141
- Wilprafen
- Turimycin A5
- Josamycine
-
SMILESCC1CC=CC=CC(C(CC(C(C(C(CC(=O)O1)OC(=O)C)OC)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)OC(=O)CC(C)C)(C)O)N(C)C)O)CC=O)C)O
-
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- Pubchem - josamycin
- Wikipedia - josamycin
Josamycin is a macrolide antibiotic. It is synthesized from strains of Streptomyces narbonensis var. josamyceticus var.
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