Compound ID | 1686

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Boromycin

Class: Macrolide

Agent Type: Natural product; Small molecule;
Spectrum of activity: Gram-negative
Mechanism of action: Membrane-active agent
Target Pathogen: Active against Helicobacter pylori
Description: Natural product from Streptomyces antibioticus; a polyether macrolide
Institute where first reported: Hokkaido University, Japan
Year first mentioned: 2018
Development status: Experimental
Chemical structure(s):
Click here for structure editor
Molecular weight: 879.88
Iso. SMILES: [B-]123OC4C(=O)O[C@@H](C/C=C/CC[C@@H](C([C@@H]5CC[C@H]([C@@](O1)(O5)C(O2)C(=O)O[C@H]6C[C@@H](CCC[C@H](C([C@@H]7CC[C@H]([C@@]4(O3)O7)C)(C)C)O)O[C@@H]6C)C)(C)C)O)[C@@H](C)OC(=O)[C@@H](C(C)C)[NH3+]
InChI Key: OOBFYEMEQCZLJL-XURNZCJASA-O
Can. SMILES: CC(C)[C@H](C(=O)O[C@H](C)[C@@H]1C/C=C/CC[C@@H](C(C)(C)[C@@H]2CC[C@@H](C)[C@]3(C4C(=O)O[C@H]5C[C@@H](CCC[C@H](C(C)(C)[C@@H]6CC[C@@H](C)[C@]7(C(C(=O)O1)O[B-](O4)(O7)O3)O6)O)O[C@@H]5C)O2)O)[NH3+]
InChI: InChI=1S/C45H73BNO15/c1-24(2)36(47)39(50)54-27(5)30-16-12-11-13-17-32(48)42(7,8)34-21-19-26(4)45(57-34)38-41(52)56-31-23-29(53-28(31)6)15-14-18-33(49)43(9,10)35-22-20-25(3)44(58-35)37(40(51)55-30)59-46(60-38,61-44)62-45/h11-12,24-38,48-49H,13-23,47H2,1-10H3/q-1/p+1/b12-11+/t25-,26-,27-,28-,29-,30+,31+,32+,33-,34+,35+,36-,37?,38?,44+,45+,46?/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6436027
Guide to Pharmacology: boromycin
Citations:
  • https://www.nature.com/articles/s41429-018-0087-2
  • https://www.nature.com/articles/s41429-018-0115-2

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