Erythromycin Cyclocarbonate

  Cat. No.:  DC8440   Featured
Chemical Structure
55224-05-0
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More than 5000 active chemicals with high quality for research!
Field of application
Erythromycin Cyclocarbonate, derivative of Erythromycin, inhibits protein synthesis of bacteria by binding to the 50S ribosome.
Cas No.: 55224-05-0
Chemical Name: cyclic 11,12-carbonate erythromycin
SMILES: CC[C@@H]1OC(=O)[C@H](C)[C@@H](OC2O[C@@H](C)[C@H](O)[C@](C)(OC)C2)[C@H](C)C(OC2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@]2([H])OC(O[C@]12C)=O
Formula: C38H65NO14
M.Wt: 759.92
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: Erythromycin Cyclocarbonate, derivative of Erythromycin, which is active against Gram-positive and some Gram-negative microorganisms.
In Vitro: Erythromycin is used in treatment of respiratory, gastrointestinal, and genital tract infections, as well as skin and soft tissue infections. Erythromycin, with its ten chiral centers and two sugar substituents (L-cladinose and D-desosamine), is a good starting point for numerous medicinal chemistry efforts for improvement of its biological profile (better activity, higher stability, and improved bioavailability) since the first generation of macrolides, which had low toxicity and good tolerability, are unstable in acidic media, had low toxicity and good tolerability[1].
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
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