Salutaridine

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Salutaridine
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Names
IUPAC name
4-Hydroxy-3,6-dimethoxy-17-methyl-5,6,8,14-tetradehydromorphinan-7-one
Other names
DNA/DNS
Identifiers
1936-18-1 YesY
ChEBI CHEBI:17225 N
ChEMBL ChEMBL404097 N
ChemSpider 21 N
Jmol 3D model Interactive image
PubChem 5408233
  • InChI=1S/C19H21NO4/c1-20-7-6-19-10-16(24-3)14(21)9-12(19)13(20)8-11-4-5-15(23-2)18(22)17(11)19/h4-5,9-10,13,22H,6-8H2,1-3H3/t13-,19+/m1/s1 N
    Key: GVTRUVGBZQJVTF-YJYMSZOUSA-N N
  • InChI=1/C19H21NO4/c1-20-7-6-19-10-16(24-3)14(21)9-12(19)13(20)8-11-4-5-15(23-2)18(22)17(11)19/h4-5,9-10,13,22H,6-8H2,1-3H3/t13-,19+/m1/s1
    Key: GVTRUVGBZQJVTF-YJYMSZOUBK
  • CN1CC[C@]23C=C(C(=O)C=C2[C@H]1CC4=C3C(=C(C=C4)OC)O)OC
Properties
CH2NO2
Molar mass 60.03 g·mol−1
Appearance 1
Density 2
Melting point 3
Boiling point 4
5
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N 376119456&page2=Salutaridine verify (what is YesYN ?)
Infobox references

Salutaridine, also known as floripavine,[1] is an alkaloid that is present in the morphinian alkaloid pathway of opium poppy. Its precursor is the alkaloid (R)-reticuline. (R)-reticuline is converted to salutaridine by the enzyme salutaridine synthase. Salutaridine is converted to salutaridinol by the enzyme salutaridine reductase (SalR), with the reduction of NADPH to NADP+.

References

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cam ICEL = H²O/O²H/CHO²

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