*Please inquire the availability for this product. Maduramicin ammonium is prepared from maduramicin by taking advantage of the acidic carboxylic acid which ionises and readily forms the salt in ammonium hydroxide solutions. The ammonium salt is the preferred formulation in animals to prevent coccidiosis and to promote growth. Maduramicin is also active against Treponema and Cryptosporidium. Maduramicin is an ionophore, forming complexes with monovalent cations, with a higher affinity for K+ than Na+.

Additional Information

Synonyms	CL 259971, Maduramycin sodium
Product #	M-2555
CAS #	84878-61-5
Formula	C47H83NO17
MW	934.2
Appearance	White solid
Purity	>98% by HPLC
Melting Point	173-176 C
Therapeutic Area	Veterinary Disorders
Use	Maduramicin ammonium salt is the preferred formulation in animals to prevent coccidiosis and to promote growth

Additional Information

MDL Number	MFCD00865282
InChI	InChI=1S/C47H81NO16.H2O/c1-23-18-24(2)45(9,51)61-36(23)31-19-32(58-35-20-30(53-10)40(55-12)28(6)57-35)42(59-31)44(8)15-14-33(60-44)43(7)16-17-46(64-43)21-29(49)25(3)37(62-46)26(4)38-41(56-13)39(54-11)27(5)47(52,63-38)22-34(48)50;/h23-33,35-42,49,51-52H,14-22H2,1-13H3,(H2,48,50);1H2/t23-,24+,25+,26+,27-,28-,29-,30-,31+,32-,33+,35+,36-,37-,38-,39-,40-,41-,42+,43-,44-,45-,46+,47+;/m0./s1
SMILES	C[C@H]1C[C@H]([C@@](O[C@@H]1[C@H]2C[C@@H]([C@@H](O2)[C@@]3(CC[C@@H](O3)[C@@]4(CC[C@@]5(O4)C[C@@H]([C@H]([C@H](O5)[C@@H](C)[C@H]6[C@@H]([C@H]([C@@H]([C@](O6)(CC(=O)N)O)C)OC)OC)C)O)C)C)O[C@@H]7C[C@@H]([C@H]([C@@H](O7)C)OC)OC)(C)O)C.O