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Chemical Structure| 35457-80-8 Chemical Structure| 35457-80-8

Structure of Midecamycin
CAS No.: 35457-80-8

Chemical Structure| 35457-80-8

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Midecamycin is a naturally occurring 16-membered macrolide antibiotic, structurely similar to erythromycin.

Synonyms: Antibiotic SF-837; SF-837; Turimycin P3

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Product Details of Midecamycin

CAS No. :35457-80-8
Formula : C41H67NO15
M.W : 813.97
SMILES Code : O[C@H]1[C@](O[C@H](C)[C@@H](O[C@@](O[C@@H](C)[C@@H]2OC(CC)=O)([H])C[C@]2(O)C)[C@@H]1N(C)C)([H])O[C@@H]([C@H](C[C@H]([C@H](/C=C/C=C/C3)O)C)CC=O)[C@H]([C@](CC(O[C@@H]3C)=O)([H])OC(CC)=O)OC
Synonyms :
Antibiotic SF-837; SF-837; Turimycin P3
MDL No. :MFCD00865000

Safety of Midecamycin

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Mycoplasma pneumoniae M129 5.12 mg/L 87 days To investigate the potential of midecamycin to induce resistance in M. pneumoniae and its mechanisms. Results showed that midecamycin is the least potent drug to induce resistance, and the induced resistance is restrained to the 16-membered macrolides. Front Cell Infect Microbiol. 2023 May 22;13:1186017
Mycoplasma pneumoniae MIC50: <0.5 µg/ml, MIC90: 16 µg/ml To evaluate the antibacterial activity of midecamycin against M. pneumoniae, results showed midecamycin exhibited the greatest activity among the three macrolides Front Cell Infect Microbiol. 2025 Mar 4;15:1496521

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.23mL

0.25mL

0.12mL

6.14mL

1.23mL

0.61mL

12.29mL

2.46mL

1.23mL

References

 

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