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Mycolactone information


Mycolactone
Names
Preferred IUPAC name
(6S,7S,9E,12R)-12-[(2S,4E,6R,7R,9R)-7,9-Dihydroxy-4,6-dimethyldec-4-en-2-yl]-7,9-dimethyl-2-oxo-1-oxacyclododec-9-en-6-yl (2E,4E,6E,8E,10E,12S,13S,15S)-12,13,15-trihydroxy-4,6,10-trimethylhexadeca-2,4,6,8,10-pentaenoate
Identifiers
CAS Number
  • 222050-77-3 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 4445303 checkY
MeSH Mycolactone
PubChem CID
  • 5282079
CompTox Dashboard (EPA)
  • DTXSID10415207 Edit this at Wikidata
InChI
  • InChI=1S/C44H70O9/c1-28(13-11-14-29(2)25-39(48)40(49)27-37(10)46)21-30(3)18-20-44(51)52-41-15-12-16-43(50)53-42(19-17-31(4)22-34(41)7)35(8)24-32(5)23-33(6)38(47)26-36(9)45/h11,13-14,17-18,20-21,23,25,33-42,45-49H,12,15-16,19,22,24,26-27H2,1-10H3/b14-11+,20-18+,28-13+,29-25+,30-21+,31-17+,32-23+/t33-,34+,35+,36-,37+,38-,39+,40+,41+,42-/m1/s1 checkY
    Key: WKTLNJXZVDLRTJ-QRRXZRELSA-N checkY
  • InChI=1/C44H70O9/c1-28(13-11-14-29(2)25-39(48)40(49)27-37(10)46)21-30(3)18-20-44(51)52-41-15-12-16-43(50)53-42(19-17-31(4)22-34(41)7)35(8)24-32(5)23-33(6)38(47)26-36(9)45/h11,13-14,17-18,20-21,23,25,33-42,45-49H,12,15-16,19,22,24,26-27H2,1-10H3/b14-11+,20-18+,28-13+,29-25+,30-21+,31-17+,32-23+/t33-,34+,35+,36-,37+,38-,39+,40+,41+,42-/m1/s1
    Key: WKTLNJXZVDLRTJ-QRRXZRELBE
SMILES
  • O=C1O[C@H](C/C=C(/C[C@@H]([C@@H](OC(=O)\C=C\C(=C\C(=C\C=C\C(=C\[C@H](O)[C@@H](O)C[C@@H](O)C)C)C)C)CCC1)C)C)[C@@H](C)CC(=C/[C@@H](C)[C@H](O)C[C@H](O)C)/C
Properties
Chemical formula
C44H70O9
Molar mass 743.021
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Mycolactone is a polyketide-derived macrolide produced and secreted by a group of very closely related pathogenic mycobacteria species including M. ulcerans, M. liflandii (an unofficial designation), M. pseudoshottsii, and some strains of M. marinum. These mycobacteria are collectively referred to as mycolactone-producing mycobacteria or MPM.[1][2]

In humans, mycolactone is the toxin responsible for Buruli ulcers, doing so by damaging tissues and inhibiting the immune response.[3]

  1. ^ Yip MJ, Porter JL, Fyfe JA, Lavender CJ, et al. (March 2007). "Evolution of Mycobacterium ulcerans and other mycolactone-producing mycobacteria from a common Mycobacterium marinum progenitor". J. Bacteriol. 189 (5): 2021–29. doi:10.1128/JB.01442-06. PMC 1855710. PMID 17172337.
  2. ^ Käser M; Hauser J; Small P; Pluschke G. (September 2009). "Large sequence polymorphisms unveil the phylogenetic relationship of environmental and pathogenic mycobacteria related to "Mycobacterium ulcerans"". Appl Environ Microbiol. 75 (17): 5667–75. Bibcode:2009ApEnM..75.5667K. doi:10.1128/AEM.00446-09. PMC 2737907. PMID 19592526.
  3. ^ "Buruli ulcer disease". Fact sheets. WHO. March 2007. Retrieved 24 March 2012.

and 7 Related for: Mycolactone information

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Mycolactone

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Mycolactone is a polyketide-derived macrolide produced and secreted by a group of very closely related pathogenic mycobacteria species including M. ulcerans...

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Mycobacterium ulcerans

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involved in the production of the toxin mycolactone. Other closely related mycobacteria produce mycolactone and infect various aquatic animals; these...

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Buruli ulcer

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open wounds. Once in the skin, M. ulcerans grows and releases the toxin mycolactone, which blocks the normal function of cells, resulting in tissue death...

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Neglected tropical diseases

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cause tuberculosis and leprosy. Mycobacterium ulcerans produces a toxin, mycolactone, that destroys tissue. The prevalence of Buruli ulcer is unknown. The...

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MLSA

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Association, a former British trade union MLSA1 and MLSA2, genes required for mycolactone biosynthesis Multilocus sequence analysis, a molecular biology technique...

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Macrolide

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produced by bacteria have been isolated and characterized, such as the mycolactones. The primary means of bacterial resistance to macrolides occurs by post-transcriptional...

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Yoshito Kishi

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accomplishments of his research group include the total syntheses of palytoxin, mycolactones, halichondrins, saxitoxin, tetrodotoxin, geldanamycin, batrachotoxin...

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