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| | septamycin Basic information |
| Product Name: | septamycin | | Synonyms: | septamycin;Antibiotic A-28695A;2H-Pyran-2-acetic acid, 6-[[(2R,3R,4R,5S,7S,9R,10R)-3,9-dimethoxy-2,4,10-trimethyl-2-[(2S,2'R,5R,5'R)-octahydro-5'-[(2S,3S,5R,6S)-tetrahydro-6-hydroxy-3,5,6-trimethyl-2H-pyran-2-yl][2,2'-bifuran]-5-yl]-1,6-dioxaspiro[4.5]dec-7-yl]methyl]tetrahydro-2-hydroxy-4-methoxy-α,3,5-trimethyl-5-[[(2S,5S,6R)-t...;A 28695A;A28695A;A-28695A | | CAS: | 54927-63-8 | | MF: | C48H82O16 | | MW: | 915.16 | | EINECS: | | | Product Categories: | | | Mol File: | 54927-63-8.mol |  |
| | septamycin Chemical Properties |
| Melting point | 101.5°C | | Boiling point | 727.06°C (rough estimate) | | density | 1.0623 (rough estimate) | | refractive index | 1.7650 (estimate) | | pka | 4.39±0.10(Predicted) |
| Toxicity | LD50 oral in rat: 10mg/kg |
| | septamycin Usage And Synthesis |
| Uses | Septamycin (A 28695A) is a metal complexing polyether antibiotic. Septamycin is produced by a strain of Streptomyces hygroscopicus NRRL 5678. Septamycin has anticoccidial activity[1][2]. | | References | [1] Meingassner JG, et, al. Laboratory studies on the anticoccidial activity of septamycin. Poult Sci. 1977 Jul;56(4):1281-8. DOI:10.3382/ps.0561281
[2] Keller-Juslén C, et, al. Septamycin, a polyether antibiotic. Taxonomy, fermentation, isolation and characterization. J Antibiot (Tokyo). 1975 Nov;28(11):854-9. DOI:10.7164/antibiotics.28.854 |
| | septamycin Preparation Products And Raw materials |
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