Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C27H35NO8 |
| Molecular Weight | 501.5687 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 6 / 6 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H]1[C@H]2C[C@H](OC(C)=O)\C=C\C(C)=C\C[C@H](O)\C=C\C(C)=C\[C@@H](NC(=O)C(C)=O)[C@](C)(C(=O)O2)C1=O
InChI
InChIKey=LSNBAGMWJRMBEO-VGBMZARNSA-N
InChI=1S/C27H35NO8/c1-15-7-10-20(31)11-8-16(2)13-23(28-25(33)18(4)29)27(6)24(32)17(3)22(36-26(27)34)14-21(12-9-15)35-19(5)30/h7-9,11-13,17,20-23,31H,10,14H2,1-6H3,(H,28,33)/b11-8+,12-9+,15-7+,16-13+/t17-,20+,21-,22-,23-,27+/m1/s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/3377458
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3377458
Sedecamycin (also known as lankacidin A), a 17-membered macrolide antibiotic that showed potent activity against Treponema hyodysenteriae. This compound was used in veterinary for treating swine dysentery.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Quinoprotein dehydrogenase functions at the final oxidation step of lankacidin biosynthesis in Streptomyces rochei 7434AN4. | 2018-08 |
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| [Simultaneous determination of sedecamycin and terdecamycin in livestock products by LC/MS]. | 2008-06 |
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| In vitro and in vivo activities of sedecamycin against Treponema hyodysenteriae. | 1988-04 |
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| Incorporation of radioactivity into fatty acids in pigs after successive administration of 14C-sedecamycin. | 1987-11 |
|
| Liquid chromatographic method for determining the macrolide antibiotic sedecamycin and its major metabolites in swine plasma and tissues. | 1987-09-01 |
Patents
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NCI_THESAURUS |
C261
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ACTIVE MOIETY