Compound ID | 2586

Update compound information

Lasalocid

Synonym(s): Lasalocid-sodium

Class: Natural product antibiotic

Spectrum of activity: Gram-positive
Details of activity: Active against Ruminococcus sp.
Description: Natural product from Streptomyces lasaliensi; an ionophore
Institute where first reported: Hoffman-LaRoche, Inc.
Year first mentioned: 1979
Development status: Active
Chemical structure(s):
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Molecular weight: 590.79
Iso. SMILES: CC[C@H]([C@@H]1[C@H](C[C@@](O1)(CC)[C@H]2CC[C@@]([C@@H](O2)C)(CC)O)C)C(=O)[C@@H](C)[C@H]([C@H](C)CCC3=C(C(=C(C=C3)C)O)C(=O)O)O
InChI Key: BBMULGJBVDDDNI-OWKLGTHSSA-N
Can. SMILES: CC[C@@H](C(=O)[C@@H](C)[C@H]([C@H](C)CCC1=CC=C(C)C(=C1C(=O)O)O)O)[C@@H]2[C@@H](C)C[C@@](CC)([C@H]3CC[C@](CC)([C@H](C)O3)O)O2
InChI: InChI=1S/C34H54O8/c1-9-25(31-21(6)18-34(11-3,42-31)26-16-17-33(40,10-2)23(8)41-26)30(37)22(7)28(35)19(4)12-14-24-15-13-20(5)29(36)27(24)32(38)39/h13,15,19,21-23,25-26,28,31,35-36,40H,9-12,14,16-18H2,1-8H3,(H,38,39)/t19-,21+,22+,23+,25+,26-,28+,31+,33-,34+/m1/s1
External links:
Citations:
  • https://pubs.acs.org/doi/10.1021/acs.langmuir.9b03752
  • https://journals.asm.org/doi/epdf/10.1128/aem.38.1.72-77.1979

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