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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 mass256.349 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

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

See also

[edit]

References

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


Ergolines
(incl.lysergines)
Clavines
(6,8-dimethylergolines)
Lysergamides
(lysergic acid amides)
Ergopeptines
(peptide ergolines)
Partial ergolines
Related compounds
Natural sources


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