Cycloclavine

Add links
Source: Wikipedia, the free encyclopedia.
Cycloclavine
Names
IUPAC name
6,8-Dimethyl-8,10-cycloergoline
Systematic IUPAC name
(1aS,3aR,9bS)-1a,3-Dimethyl-1a,2,3,3a,4,6-hexahydro-1H-cyclopropa[c]indolo[4,3-ef]indole
Identifiers
3D model (
JSmol
)
ChemSpider
UNII
  • InChI=1S/C16H18N2/c1-15-8-16(15)11-4-3-5-12-14(11)10(7-17-12)6-13(16)18(2)9-15/h3-5,7,13,17H,6,8-9H2,1-2H3/t13-,15-,16-/m0/s1
    Key: ZWJHDICNUKHUGE-BPUTZDHNSA-N
  • [H][C@@]12CC3=CNC4=C3C(=CC=C4)[C@]11C[C@]1(C)CN2C
Properties
C16H18N2
Molar mass 238.334 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Cycloclavine is an

LSD (lysergic acid diethylamide), psilocin, and DMT. Differential 5-HT receptor affinities, as well as novel sigma-1 receptor properties, suggest potential future therapeutic opportunities of clavine alkaloid
scaffolds.

References

  1. ^ "KNApSAcK Metabolite Information - C00011221". www.knapsackfamily.com.
  2. PMID 5373534
    .
  3. doi:10.1016/j.tet.2008.01.101
    .
  4. PMID 21517102
    .
  5. PMID 24279324
    .
  6. PMID 24511164
    .
  7. PMID 27860203
    .
  8. ISSN 0039-7881
    .



Stub icon

This article about an alkaloid is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Cycloclavine&oldid=1152493827"