Jump to content

Chanoclavine II

From Wikipedia, the free encyclopedia
Chanoclavine II
Names
Preferred IUPAC name
(2E)-2-Methyl-3-[(4R,5S)-4-(methylamino)-1,3,4,5-tetrahydrobenzo[cd]indol-5-yl]prop-2-en-1-ol
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C16H20N2O/c1-10(9-19)6-13-12-4-3-5-14-16(12)11(8-18-14)7-15(13)17-2/h3-6,8,13,15,17-19H,7,9H2,1-2H3/b10-6+/t13-,15+/m0/s1
    Key: SAHHMCVYMGARBT-GJTNBUKJSA-N
  • InChI=1/C16H20N2O/c1-10(9-19)6-13-12-4-3-5-14-16(12)11(8-18-14)7-15(13)17-2/h3-6,8,13,15,17-19H,7,9H2,1-2H3/b10-6+/t13-,15+/m0/s1
    Key: SAHHMCVYMGARBT-GJTNBUKJBF
  • C/C(=C\[C@@H]1[C@@H](CC2=CNC3=CC=CC1=C23)NC)/CO
Properties
C16H20N2O
Molar mass 256.349 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Chanoclavine II is an ergoline compound produced by certain fungi.[1]

See also

[edit]

References

[edit]
  1. ^ Stauffacher, D.; Tscherter, N. (1964). "Ergot alkaloids. LXIII. Isomers of chanoclavine from Claviceps purpurea". Helvetica Chimica Acta. 47 (8): 2186–2194.{{cite journal}}: CS1 maint: multiple names: authors list (link)



Stub icon

This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Chanoclavine_II&oldid=1272663732"