Maduramicin

Maduramicin
Clinical data
Other names	Maduramycin
AHFS/Drugs.com	International Drug Names
ATCvet code	QP51BB05 (WHO) ;
Identifiers
CAS Number	84878-61-5 ; acid: 79356-08-4 ;
PubChem CID	68595;
ChemSpider	61862;
UNII	5U912U22T2; acid: 6S6GVE3CIQ ;
ChEMBL	ChEMBL1909066;
Chemical and physical data
Formula	C47H80O17
Molar mass	917.140 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O=C(O)C[C@@]1(O)O[C@H]([C@H](OC)[C@@H](OC)[C@@H]1C)[C@H](C)[C@H]7O[C@]6(O[C@](C)([C@@H]5O[C@](C)([C@@H]4O[C@@H]([C@H]2O[C@@](O)(C)[C@H](C)C[C@@H]2C)C[C@@H]4O[C@H]3O[C@@H](C)[C@H](OC)[C@@H](OC)C3)CC5)CC6)C[C@H](O)[C@H]7C;

Maduramicin

Chemical compound

Maduramicin (maduramycin) is an antiprotozoal agent used in veterinary medicine to prevent coccidiosis.^[1]^[2] It is a natural chemical compound first isolated from the actinomycete Actinomadura rubra.^[3]

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[1] [1]
Maduramicin Ammonium, Canadian Food Inspection Agency

[2] [2]
McDougald LR, Fuller AL, Mathis GF, Wang GT (1990). "Efficacy of maduramicin ammonium against coccidiosis in turkeys under laboratory and floor-pen conditions". Avian Diseases. 34 (3): 634–638. doi:10.2307/1591256. JSTOR 1591256. PMID 2241692.

[3] [3]
Fleck WF, Strauss DG, Meyer J, Porstendorfer G (1978). "Fermentation, isolation, and biological activity of maduramycin: a new antibiotic from Actinomadura rubra". Zeitschrift für Allgemeine Mikrobiologie. 18 (6): 389–398. doi:10.1002/jobm.3630180602 (inactive 31 January 2024). PMID 362738.{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)

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Maduramicin

References

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