Compound ID | 3307

Update compound information

CP-54,883

Synonym(s): CP-54883  |  CP-54 883  |  CP54883  |  CP 54 883  |  CP 54883

Class: Natural product antibiotic (polyether)

Spectrum of activity: Gram-positive
Details of activity: Active against Staphylococcus aureus, Streptococcus pyogenes, Enterococcus faecalis, and Staphylococcus epidermidis
Description: Natural product from Actinomadura routienii; a polyether
Institute where first reported: Pfizer
Year first mentioned: 1987
Development status: Experimental
Chemical structure(s):
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Molecular weight: 817.83
Iso. SMILES: CC1CC(C(OC1CC2CC(C(C3(O2)C(CC(O3)(C)C4CCC(O4)(C)C(C(C(C)OC(=O)C5=C(C(=CC(=C5O)Cl)Cl)C)OC)O)C)C)OC)C(C)C(=O)O)C
InChI Key: TVMWRYCBZQKLFO-UHFFFAOYSA-N
Can. SMILES: CC1CC(C)C(C(C)C(=O)O)OC1CC2CC(C(C)C3(C(C)CC(C)(C4CCC(C)(C(C(C(C)OC(=O)C5=C(C(=CC(=C5C)Cl)Cl)O)OC)O)O4)O3)O2)OC
InChI: InChI=1S/C41H62Cl2O12/c1-19-14-20(2)34(23(5)37(46)47)52-29(19)15-26-16-30(49-10)24(6)41(53-26)21(3)18-40(9,55-41)31-12-13-39(8,54-31)36(45)35(50-11)25(7)51-38(48)32-22(4)27(42)17-28(43)33(32)44/h17,19-21,23-26,29-31,34-36,44-45H,12-16,18H2,1-11H3,(H,46,47)
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/3082643
Citations:
  • https://www.jstage.jst.go.jp/article/antibiotics1968/40/11/40_11_1496/_article/-char/en
  • https://www.jstage.jst.go.jp/article/antibiotics1968/40/11/40_11_1490/_article/-char/en

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