Lycoctonine

Lycoctonine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C25H41NO7/c1-6-26-11-22(12-27)8-7-16(31-3)24-14-9-13-15(30-2)10-23(28,17(14)18(13)32-4)25(29,21(24)26)20(33-5)19(22)24/h13-21,27-29H,6-12H2,1-5H3/t13-,14-,15+,16+,17-,18+,19-,20+,21+,22+,23-,24+,25+/m1/s1
    Key: YOTUXHIWBVZAJQ-VCDUNCIKSA-N
  • CCN1C[C@@]2(CC[C@@H]([C@@]34[C@@H]2[C@@H]([C@]([C@H]31)([C@]5(C[C@@H]([C@H]6C[C@@H]4[C@@H]5[C@H]6OC)OC)O)O)OC)OC)CO
Properties
C25H41NO7
Molar mass 467.603 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Lycoctonine is a plant alkaloid and a precursor to the ABC ring system of taxoids. Distinguish from lycaconitine, which is the N-succinimido-benzoic-ester.

  • Liang XX, Tang P, Chen QH, Wang FP (June 2012). "Synthesis of taxane ABC tricyclic skeleton from lycoctonine". Natural Product Communications. 7 (6) 1934578X1200700603: 697–703. doi:10.1177/1934578X1200700603. PMID 22816287.
  • Hohmann J, Forgo P, Hajdú Z, Varga E, Máthé I (July 2002). "Norditerpenoid alkaloids from Consolida orientalis and complete 1H and 13C NMR signal assignments of some lycoctonine-type alkaloids". Journal of Natural Products. 65 (7): 1069–72. Bibcode:2002JNAtP..65.1069H. doi:10.1021/np020026z. PMID 12141879.