Compound ID | 2108

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Muraminomicin

Synonym(s): Muraminomycin

Class: Natural product antibiotic

Spectrum of activity: Gram-positive
Details of activity: Interferes with cell-wall synthesis by inhibiting transfer of the peptidoglycan precursor moiety (MurNAc-pentapeptide) to the membrane lipid carrier, undecaprenyl phosphate. Activity against Mycobacterium tuberculosis
Description: Natural product produced by Streptosporangium, structurally related to liposidomycin
Year first mentioned: 2012
Development status: Experimental
Chemical structure(s):
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Molecular weight: 1184.29
Iso. SMILES: CCCCCCC=CCCCC(CC(=O)OC1CN(C(C(=O)N(C1C(=O)O)C)C([C@@H]2[C@H](C[C@@H](O2)N3C=CC(=O)NC3=O)O)O[C@H]4C[C@@H]([C@H](O4)CN)O)C)OC(=O)CC(C)CC(=O)OC5C(C(C(C(O5)CC)OC)OC(=O)CCC(=O)O)OC
InChI Key: LXKJGNPMKQBMAB-IPSUJDRFSA-N
Can. SMILES: CCCCCCC=CCCCC(CC(=O)OC1CN(C)C(C([C@@H]2[C@H](C[C@H](N3C=CC(=O)NC3=O)O2)O)O[C@H]4C[C@@H]([C@@H](CN)O4)O)C(=O)N(C)C1C(=O)O)OC(=O)CC(C)CC(=O)OC5C(C(C(C(CC)O5)OC)OC(=O)CCC(=O)O)OC
InChI: InChI=1S/C55H85N5O23/c1-8-10-11-12-13-14-15-16-17-18-31(76-41(67)23-30(3)24-42(68)82-54-51(75-7)50(48(74-6)34(9-2)79-54)81-40(66)20-19-39(64)65)25-43(69)77-36-29-58(4)46(52(70)59(5)45(36)53(71)72)49(83-44-27-32(61)35(28-56)78-44)47-33(62)26-38(80-47)60-22-21-37(63)57-55(60)73/h14-15,21-22,30-36,38,44-51,54,61-62H,8-13,16-20,23-29,56H2,1-7H3,(H,64,65)(H,71,72)(H,57,63,73)/t30?,31?,32-,33-,34?,35+,36?,38+,44-,45?,46?,47-,48?,49?,50?,51?,54?/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/145720725
Citations:
  • https://pubmed.ncbi.nlm.nih.gov/31558775/
  • https://www.nature.com/articles/s41429-019-0241-5.pdf
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588599/

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