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Chanoclavine II

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Chanoclavine II
Names
Preferred IUPAC name (2E)-2-Methyl-3-indol-5-yl]prop-2-en-1-ol
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • 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/s1Key: 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/s1Key: SAHHMCVYMGARBT-GJTNBUKJBF
SMILES
  • C/C(=C\1(CC2=CNC3=CC=CC1=C23)NC)/CO
Properties
Chemical formula C16H20N2O
Molar mass 256.349 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Chanoclavine II is an ergoline compound produced by certain fungi.

See also

References


Ergolines
Lysergic acid
derivatives
Psychedelic
lysergamides
Clavines
Other
ergolines
Related
compounds
Natural
sources

Morning glory: Argyreia nervosa (Hawaiian Baby Woodrose), Ipomoea spp.(Morning Glory, Tlitliltzin, Badoh Negro), Rivea corymbosa (Coaxihuitl, Ololiúqui)


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