Compound ID | 2584

Update compound information

Lankamycin

Class: Macrolide

Spectrum of activity: Gram-positive
Details of activity: Active against Staphylococcus aureus; inhibits protein synthesis
Description: Natural product from Streptomyces rochei
Year first mentioned: 1994
Development status: Experimental
Chemical structure(s):
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Molecular weight: 833.01
Iso. SMILES: C[C@@H]1C[C@@H]([C@H]([C@@H](O1)O[C@H]2[C@H](C[C@](C(=O)[C@@H]([C@H]([C@H]([C@H](OC(=O)[C@@H]([C@H]([C@@H]2C)O[C@H]3C[C@@]([C@@H]([C@@H](O3)C)OC(=O)C)(C)OC)C)[C@@H](C)[C@H](C)O)C)OC(=O)C)C)(C)O)C)O)OC
InChI Key: JQMACDQCTNFQMM-QAOHEUSVSA-N
Can. SMILES: C[C@H]1C[C@@](C)(C(=O)[C@H](C)[C@H]([C@@H](C)[C@@H]([C@@H](C)[C@H](C)O)OC(=O)[C@H](C)[C@H]([C@H](C)[C@H]1O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)OC)O)O[C@H]3C[C@](C)([C@@H]([C@H](C)O3)OC(=O)C)OC)OC(=O)C)O
InChI: InChI=1S/C42H72O16/c1-19-17-41(12,49)37(47)24(6)35(54-28(10)44)23(5)34(21(3)26(8)43)57-39(48)25(7)36(22(4)33(19)58-40-32(46)30(50-14)16-20(2)52-40)56-31-18-42(13,51-15)38(27(9)53-31)55-29(11)45/h19-27,30-36,38,40,43,46,49H,16-18H2,1-15H3/t19-,20+,21-,22+,23-,24+,25+,26-,27-,30-,31-,32+,33-,34+,35-,36-,38+,40-,41-,42+/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/15560071
Citations:
  • https://journals.asm.org/doi/10.1128/aac.00016-06
  • https://www.pnas.org/doi/full/10.1073/pnas.1019406108

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