Lysergol

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Lysergol
Lysergol.svg
Names
IUPAC name
(7-Methyl-4,6,6a,7,8,9-hexahydro-indolo[4,3-fg]quinolin-9-yl)-methanol
Identifiers
602-85-7 N
ChEBI CHEBI:60528 YesY
ChEMBL ChEMBL39947 YesY
ChemSpider 14267 YesY
123
Jmol 3D model Interactive image
PubChem 14987
  • InChI=1S/C16H18N2O/c1-18-8-10(9-19)5-13-12-3-2-4-14-16(12)11(7-17-14)6-15(13)18/h2-5,7,10,15,17,19H,6,8-9H2,1H3/t10-,15-/m1/s1 YesY
    Key: BIXJFIJYBLJTMK-MEBBXXQBSA-N YesY
  • InChI=1/C16H18N2O/c1-18-8-10(9-19)5-13-12-3-2-4-14-16(12)11(7-17-14)6-15(13)18/h2-5,7,10,15,17,19H,6,8-9H2,1H3/t10-,15-/m1/s1
    Key: BIXJFIJYBLJTMK-MEBBXXQBBQ
  • OC[C@@H]3/C=C2/c4cccc1c4c(cn1)C[C@H]2N(C3)C
Properties
C16H18N2O
Molar mass 254.33 g/mol
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Lysergol is an alkaloid of the ergoline family that occurs as a minor constituent in some species of fungi (most within Claviceps), and in the morning glory family of plants (Convolvulaceae), including the hallucinogenic seeds of Rivea corymbosa (ololiuhqui), Argyreia nervosa (Hawaiian baby woodrose) and Ipomoea violacea. Lysergol is not a controlled substance in the USA. Its possession and sale is also legal under the U.S. Federal Analog Act because of it does not have a known pharmacological action or a precursor relationship to LSD, which is a controlled substance. However, lysergol can be utilized as an intermediate in the manufacture of some ergoloid medicines (e.g. nicergoline).

See also

External links

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