Compound ID | 2629

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Musettamycin

Class: Natural product antibiotic

Spectrum of activity: Gram-positive
Details of activity: Active against Streptococcus pneumoniae, Streptococcus pyogenes, and Staphylococcus aureus
Description: Natural product from Actinosporangium sp.; also shows anti-tumour properties in mice; an anthracycline
Institute where first reported: Research Division, Bristol Laboratories, Division of Bristol Myers Company, Syracuse, N. Y., U. S. A
Year first mentioned: 1977
Development status: Experimental
Chemical structure(s):
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Molecular weight: 715.74
Iso. SMILES: CC[C@]1(C[C@@H](C2=C(C3=C(C=C2[C@H]1C(=O)OC)C(=O)C4=C(C=CC(=C4C3=O)O)O)O)O[C@H]5C[C@@H]([C@@H](C(O5)C)O[C@H]6C[C@@H]([C@@H]([C@@H](O6)C)O)O)N(C)C)O
InChI Key: PXKJRTZJMGPOGS-YBVXKORNSA-N
Can. SMILES: CC[C@]1(C[C@@H](C2=C(C=C3C(=C2O)C(=O)C4=C(C(=CC=C4O)O)C3=O)[C@H]1C(=O)OC)O[C@H]5C[C@@H]([C@@H](C(C)O5)O[C@H]6C[C@@H]([C@@H]([C@H](C)O6)O)O)N(C)C)O
InChI: InChI=1S/C36H45NO14/c1-7-36(46)13-22(50-23-11-18(37(4)5)34(15(3)49-23)51-24-12-21(40)30(41)14(2)48-24)25-16(29(36)35(45)47-6)10-17-26(32(25)43)33(44)28-20(39)9-8-19(38)27(28)31(17)42/h8-10,14-15,18,21-24,29-30,34,38-41,43,46H,7,11-13H2,1-6H3/t14-,15?,18-,21-,22-,23-,24-,29-,30+,34+,36+/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/99345
Citations:
  • https://www.jstage.jst.go.jp/article/antibiotics1968/30/6/30_6_519/_pdf
  • https://www.jstage.jst.go.jp/article/antibiotics1968/30/6/30_6_525/_pdf/-char/en
    • Patent: US4064014A

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