Compound ID | 2702

Update compound information

CP-84,657

Class: Natural product antibiotic

Spectrum of activity: Gram-positive
Details of activity: Active against Streptococcus suis, Clostridium perfringens, and Staphylococcus aureus
Description: Natural product from Actinomadura sp.; also has anticoccidial activity; structurally related to portmicin
Institute where first reported: Central Research, Pfizer Inc., USA
Year first mentioned: 1990
Development status: Experimental
Chemical structure(s):
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Molecular weight: 843.09
Iso. SMILES: CC[C@H]([C@@]1(C[C@@H]([C@](O1)([C@H]2C[C@@H]([C@@H](O2)[C@@]3(C[C@H]([C@@H](O3)[C@@]4(CC[C@@]5(O4)[C@@H]([C@@H]([C@H]([C@H](O5)[C@@H](C)[C@H]([C@H](C)C(=O)O)OC)C)OC)C)C)O[C@H]6CC[C@@H]([C@H](O6)C)OC)C)C)O)C)C)O
InChI Key: GCWRBUNCTDXUMB-JYAWKEJFSA-N
Can. SMILES: CC[C@H]([C@]1(C)C[C@H](C)[C@]([C@H]2C[C@H](C)[C@H]([C@]3(C)C[C@H]([C@H]([C@]4(C)CC[C@]5([C@H](C)[C@@H]([C@@H](C)[C@@H]([C@@H](C)[C@H]([C@H](C)C(=O)O)OC)O5)OC)O4)O3)O[C@H]6CC[C@@H]([C@@H](C)O6)OC)O2)(O)O1)O
InChI: InChI=1S/C45H78O14/c1-15-32(46)42(10)21-24(3)45(49,59-42)33-20-23(2)38(55-33)43(11)22-31(54-34-17-16-30(50-12)29(8)53-34)39(57-43)41(9)18-19-44(58-41)28(7)37(52-14)26(5)36(56-44)25(4)35(51-13)27(6)40(47)48/h23-39,46,49H,15-22H2,1-14H3,(H,47,48)/t23-,24-,25-,26-,27-,28+,29+,30-,31+,32+,33+,34-,35+,36+,37+,38+,39+,41-,42-,43-,44+,45-/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/9919017
Citations:
  • https://www.tandfonline.com/doi/full/10.1517/17460440802661443
  • https://www.jstage.jst.go.jp/article/antibiotics1968/43/6/43_6_668/_pdf/-char/en

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