Herkinorin

Source: Wikipedia, the free encyclopedia.
Herkinorin
Clinical data
ATC code
  • none
Legal status
Legal status
  • Legal/Uncontrolled
Identifiers
  • methyl (2S,4aR,6aR,7R,9S,10aS,10bR)-9-benzoyloxy-2-(furan-3-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate
JSmol)
  • O=C(OC)[C@H]3[C@@]4(CC[C@H]5C(=O)O[C@H](c1ccoc1)C[C@@]5([C@H]4C(=O)[C@@H](OC(=O)c2ccccc2)C3)C)C
  • InChI=1S/C28H30O8/c1-27-11-9-18-26(32)36-21(17-10-12-34-15-17)14-28(18,2)23(27)22(29)20(13-19(27)25(31)33-3)35-24(30)16-7-5-4-6-8-16/h4-8,10,12,15,18-21,23H,9,11,13-14H2,1-3H3/t18-,19-,20-,21-,23-,27-,28-/m0/s1 checkY
  • Key:PYDQMXRFUVDCHC-XAGHGKQISA-N checkY
 ☒NcheckY (what is this?)  (verify)

Herkinorin is an

diterpenes, the family of chemical compounds of which salvinorin A is a member.[1]

Unlike salvinorin A, which is a selective

deacetylation, since, while both salvinorin A and salvinorin B are found in the plant Salvia divinorum, salvinorin A is present in larger quantities.[4]

A study in primates showed it to act

arrestins.[8]

See also

References

  1. PMID 16033256
    .
  2. PMID 16792410
    .
  3. PMID 17904842
    .
  4. PMID 15380207
    .
  5. PMID 18593955
    .
  6. PMID 17090705
    .
  7. S2CID 23678472
    .
  8. PMID 18380425
    .
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