Communesin B

Communesin B is a cytotoxic fungi isolate.[1]

Communesin B
Names
Preferred IUPAC name
(2E,4E)-1-{(3aR,8aR,13bR,16aS,17S)-17-[(2R)-3,3-Dimethyloxiran-2-yl]-9-methyl-2,3,8a,9,14,15-hexahydro-8H-13,16-methanobenzo[c]indolo[3,2-j]pyrrolo[3,2-e][2,6]naphthyridin-1(16aH)-yl}hexa-2,4-dien-1-one
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C32H36N4O2/c1-5-6-7-15-24(37)35-18-16-31-21-12-8-9-13-22(21)33-28-32(31)17-19-36(29(31)35)26(27-30(2,3)38-27)20-11-10-14-23(25(20)32)34(28)4/h5-15,26-29,33H,16-19H2,1-4H3/b6-5+,15-7+/t26-,27+,28+,29+,31-,32-/m0/s1
    Key: XZFSMUXVAYCHFO-RPCCRITPSA-N
  • C/C=C/C=C/C(=O)N1CC[C@]23[C@H]1N4CC[C@@]25c6c(cccc6N([C@H]5Nc7c3cccc7)C)[C@H]4[C@@H]8C(O8)(C)C
Properties
C32H36N4O2
Molar mass 508.666 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

References
  1. Crawley, SL; Funk, RL (2003). "A synthetic approach to nomofungin/communesin B". Organic Letters. 5 (18): 3169–71. doi:10.1021/ol034407v. PMID 12943379.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.