Maduramicin α
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Maduramicin α
structure -
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CAS No:
79356-08-4
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Formula:
C47H80O17
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Chemical Name:
Maduramicin α
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Synonyms:
Maduramicin α;1,6-Dioxaspiro[4.5]decane,maduramicin α deriv.;(29S)-9,13:17,20:21,24-Trianhydro-2,4,8,10,12,14,15,18,19,23,26,27,28,30-tetradecadeoxy-4,8,10,26,28-pentamethyl-16,20-di-C-methyl-5,6-di-O-methyl-22-[(2,6-dideoxy-3,4-di-O-methyl-β-L-arabinopyranosyl)oxy]-L-glycero-L-allo-α-D-allo-L-xylo-α-L-gluco-3,13,29-triacontotriulo-13,16-furanose-3,7:29,25-dipyranosonic acid;Antibiotic X 14868A;Maduramicin;Maduramycin;119758-39-3
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CAS No:
Safety Information
|Danger|H300 (100%): Fatal if swallowed [Danger Acute toxicity, oral]|P262, P264, P270, P280, P301+P310, P302+P350, P305+P351+P338, P310, P321, P322, P330, P337+P313, P361, P363, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Maduramicin α Use and Manufacturing
Maduramicin is a polyether antibiotic first isolated from Actinomadura yunnaense (formerly Nocardia sp. X-14868) in 1963. Maduramicin is a broad spectrum anticoccidial also active against Treponema and Cryptosporidium. Maduramicin is an ionophore, forming complexes with monovalent cations, with a higher affinity for K+ than Na+. Maduramicin is used as the ammonium salt in animals to prevent coccidiosis and to promote growth.
Computed Properties
Molecular Weight:917.1
XLogP3:3.9
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:17
Rotatable Bond Count:13
Exact Mass:916.53955108
Monoisotopic Mass:916.53955108
Topological Polar Surface Area:209
Heavy Atom Count:64
Complexity:1610
Defined Atom Stereocenter Count:24
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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