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Midecamycin
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Midecamycin

CAS: 35457-80-8

Ref. 3D-AM16806

1g
295.00 €
2g
503.00 €
100mg
81.00 €
250mg
120.00 €
500mg
186.00 €
Estimated delivery in United States, on Monday 3 Jun 2024

Product Information

Name:
Midecamycin
Synonyms:
  • Leucomycin V 3,4B-dipropanoateAborenAntibiotic SF 837
  • (4R,5S,6S,7R,9R,10R,11E,13E,16R)-6-{[(2S,3R,4R,5S,6R)-4-(Dimethylamino)-3-hydroxy-5-{[(2S,4R,5S,6S)-4-hydroxy-4,6-dimethyl-5-(propionyloxy)tetrahydro-2H-pyran-2-yl]oxy}-6-methyltetrahydro-2H-pyran-2-yl]oxy}-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-4-yl propanoate (non-preferred name)
  • (4R,5S,6S,7R,9R,10R,11E,13E,16R)-6-{[(2S,3R,4R,5S,6R)-4-(dimethylamino)-3-hydroxy-5-{[(2S,4R,5S,6S)-4-hydroxy-4,6-dimethyl-5-(propanoyloxy)tetrahydro-2H-pyran-2-yl]oxy}-6-methyltetrahydro-2H-pyran-2-yl]oxy}-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-4-yl propanoate (non-preferred name)
  • 252-578-0
  • Aboren
  • Antibiotic SF 837
  • Antibiotic SF 837A<sub>1</sub>
  • Antibiotic YL 704B1
  • Antibiotic YL 704B<sub>1</sub>
  • De 4',4''-Dipropionate (Ester)
  • See more synonyms
  • Espinomycin A
  • Leucomycin V 3,4B-Dipropanoate
  • Leucomycin V, 3,4<sup>B</sup>-dipropanoate
  • Macro-Dil
  • Macropen
  • Medecamycin A<sub>1</sub>
  • Medemycin A<sub>1</sub>
  • Midecamycin A<sub>1</sub>
  • Midecin
  • Momicine
  • Mydecamycin
  • Mydecamycin A<sub>1</sub>
  • Myoxam
  • NSC 154011
  • Normicina
  • Oxacyclohexadecane, leucomycin V deriv.
  • Platenomycin B<sub>1</sub>
  • Rubimycin
  • SF 837A<sub>1</sub>
  • Sf 837
  • Turimycin P<sub>3</sub>
  • YL 704B<sub>1</sub>
Description:

Midecamycin is a macrolide antibiotic that is a covalent inhibitor of the ryanodine receptor, which regulates calcium release in muscle cells. Midecamycin has been shown to have antimicrobial activity against infectious diseases and bowel disease. It also inhibits the release of IL-2 in response to IL-2 receptor binding, which may be due to its ability to inhibit the enzyme activities of protein kinase C and phosphodiesterase. This drug also causes liver lesions, as well as enzyme inactivation. Midecamycin is not metabolized by cytochrome P450 enzymes, but does inhibit CYP3A4 and CYP2D6. Midecamycin interacts with oral cephalosporins such as cefuroxime axetil, cefpodoxime proxetil, and ceftibuten.

Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
813.97 g/mol
Formula:
C41H67NO15
Purity:
Min. 95%
Color/Form:
Powder
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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