Compound ID | 2618

Update compound information

Methymycin

Class: Macrolide

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Broad-spectrum activity; protein synthesis inhibitor
Description: Natural product from Streptomyces venezuelae
Year first mentioned: 1968
Development status: Experimental
Chemical structure(s):
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Molecular weight: 469.61
Iso. SMILES: CC[C@@H]1[C@@](/C=C/C(=O)[C@@H](C[C@@H]([C@@H]([C@H](C(=O)O1)C)O[C@H]2[C@@H]([C@H](C[C@H](O2)C)N(C)C)O)C)C)(C)O
InChI Key: HUKYPYXOBINMND-HYUJHOPRSA-N
Can. SMILES: CC[C@@H]1[C@](C)(/C=C/C(=O)[C@H](C)C[C@H](C)[C@@H]([C@@H](C)C(=O)O1)O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)O
InChI: InChI=1S/C25H43NO7/c1-9-20-25(6,30)11-10-19(27)14(2)12-15(3)22(17(5)23(29)32-20)33-24-21(28)18(26(7)8)13-16(4)31-24/h10-11,14-18,20-22,24,28,30H,9,12-13H2,1-8H3/b11-10+/t14-,15+,16-,17-,18+,20-,21-,22+,24+,25+/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/5282034
Citations:
  • https://www.pnas.org/doi/full/10.1073/pnas.95.21.12111
  • https://academic.oup.com/nar/article/45/16/9573/4056244?login=true#108560249
    • Patents:
  • US2916483A
  • WO2000000620A3
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