Maduramicin ammonium

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Names

[ CAS No. ]:
84878-61-5

[ Name ]:
Maduramicin ammonium

[Synonym ]:
MADUBAMYCIN AMMONIUM
[(2R,3S,4S,5R,6S)-6-{(1R)-1-[(2S,5R,7S,8R,9S)-2-{(2S,2'R,3'S,5R,5'R)-3'-{[(2R,4S,5S,6S)-4,5-Dimethoxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-5'-[(2S,3S,5R,6S)-6-hydroxy-3,5,6-trimethyltetrahydro-2H-pyran-2-yl]-2-methyloctahydro-2,2'-bifuran-5-yl}-9-hydroxy-2,8-dimethyl-1,6-dioxaspiro[4.5]dec-7-yl]ethyl}-2-hydroxy-4,5-dimethoxy-3-methyltetrahydro-2H-pyran-2-yl]acetic acid ammoniate (1:1) (non-preferred name)
Maduramicin
Maduramicin ammonium
MADURAMICINAMMONIUM
MADURAMINIC AMMONIUM
Maduramycin
Maduramycin ammonium
MADURAMICIN AMMONIUM PREMIX

Chemical & Physical Properties

[ Boiling Point ]:
913.9ºC at 760 mmHg

[ Melting Point ]:
173-176ºC

[ Molecular Formula ]:
C47H83NO17

[ Molecular Weight ]:
934.158

[ Flash Point ]:
255.5ºC

[ Exact Mass ]:
933.566101

[ PSA ]:
211.58000

[ LogP ]:
3.35840

[ Storage condition ]:
0-6°C

Safety Information

[ Symbol ]:

GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H300 + H310-H319

[ Precautionary Statements ]:
Missing Phrase - N15.00950417-P262-P280-P302 + P352 + P310-P305 + P351 + P338-P361 + P364

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
T+:Verytoxic;

[ Risk Phrases ]:
R25;R27;R36

[ Safety Phrases ]:
S26-S28-S36/37-S45

[ RIDADR ]:
UN 2811

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

Articles

Maduramicin inhibits proliferation and induces apoptosis in myoblast cells.

PLoS ONE 9(12) , e115652, (2014)

Maduramicin, a polyether ionophore antibiotic derived from the bacterium Actinomadura yumaensis, is currently used as a feed additive against coccidiosis in poultry worldwide. It has been clinically o...


More Articles


Related Compounds

  • Maduramicin ammonium
  • Maduramicin
  • maduramicin
  • propenoate, ammonium salt
  • Quaternary ammonium compounds, C12-18-alkyl[2-(C12-22-unsatd. acyloxy)ethyl]dimethyl, chlorides
  • Quaternary ammonium compounds, C14-18-alkylethyldimethyl, phenoxides
  • 3-(5-bromo-2-thienyl)-1-methyl-1H-pyrazole-5-carboxylic acid
  • 3-[({[2-(2-Fluorophenyl)-1,3-thiazol-4-yl]acetyl}amino)methyl]benzoic acid
  • N-[3-(acetylamino)phenyl]-4-(3-oxo-1,2-benzothiazol-2(3H)-yl)butanamide
  • N-[2-(2-methoxyphenyl)ethyl]-1-(propan-2-yl)-1,5,6,7-tetrahydrocyclopenta[b]pyrazolo[4,3-e]pyridine-4-carboxamide
  • N-(3,5-dimethoxyphenyl)-2-(3-ethyl-4-oxo-7-phenyl-3,4-dihydro-5H-pyrrolo[3,2-d]pyrimidin-5-yl)acetamide
  • 1-[4-(diethylsulfamoyl)phenyl]-5-oxo-N-(pyridin-2-ylmethyl)pyrrolidine-3-carboxamide
  • N-[(2E)-5-(methoxymethyl)-1,3,4-thiadiazol-2(3H)-ylidene]-2-(4-oxo-1,2,3-benzotriazin-3(4H)-yl)acetamide
  • N-(4-fluorobenzyl)-N-(furan-2-ylmethyl)-3-phenyl-5,6-dihydro-1,4-oxathiine-2-carboxamide 4,4-dioxide
  • N-{[2-(3-chlorophenyl)-1,3-thiazol-4-yl]acetyl}glycine
  • 4-[4-(1,2-benzisothiazol-3-yl)piperazino]-N-(4-hydroxyphenyl)-4-oxobutanamide
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