| Weight | 843.065 g/mol |
|---|---|
| Formula | C43H74N2O14 |
| Hydrogen Acceptors | 16 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 11 |
spiramycin (8025-81-8)
Score:
#310 in Microbiology
,
#995 in Biochemistry
,
#2617 in Biology
,
#3270 in Chemistry
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- Erythromycin, carbomycin, and spiramycin inhibit protein synthesis by stimulating the dissociation of peptidyl-tRNA from ribosomes. (Antimicrobial Agents and Chemotherapy, 1982)
- Treatment of Intestinal Cryptosporidiosis with Spiramycin (Annals of Internal Medicine, 1984)
- Inhibition of the ribosomal peptidyl transferase reaction by the mycarose moiety of the antibiotics carbomycin, spiramycin and tylosin (Journal of Molecular Biology, 2000)
- Mechanism of action of spiramycin and other macrolides (Journal of Antimicrobial Chemotherapy, 1988)
- Quantitative in Vitro Evaluation of the Energy Metabolism Influenced by Virginiamycin and Spiramycin used as Growth Promoters in Pig Nutrition1 (Journal of Animal Science, 1979)
- Prophylaxis of congenital toxoplasmosis. Effects of spiramycin on placental infection (Journal of Antimicrobial Chemotherapy, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1CC=CC=CC(C(CC(C(C(C(CC(=O)O1)O)OC)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)O)(C)O)N(C)C)O)CC=O)C)OC4CCC(C(O4)C)N(C)C
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InChIKeyACTOXUHEUCPTEW-UHFFFAOYSA-N
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