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7,8-didehydro-4,5-epoxymorphinan-3,6-diol

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q116395575
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7,8-didehydro-4,5-epoxymorphinan-3,6-diol

Summary

7,8-didehydro-4,5-epoxymorphinan-3,6-diol is a group of stereoisomers[1].

Key Facts

  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's instance of is recorded as group of stereoisomers[2].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's canonical SMILES is recorded as C1CNC2CC3=C4C15C2C=CC(C5OC4=C(C=C3)O)O[3].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's InChI is recorded as InChI=1S/C16H17NO3/c18-11-3-1-8-7-10-9-2-4-12(19)15-16(9,5-6-17-10)13(8)14(11)20-15/h1-4,9-10,12,15,17-19H,5-7H2[4].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's InChIKey is recorded as ONBWJWYUHXVEJS-UHFFFAOYSA-N[5].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's chemical formula is recorded as C₁₆H₁₇NO₃[6].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's subclass of is recorded as morphinan alkaloid[7].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's ChemSpider ID is recorded as 380506[8].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's PubChem CID is recorded as 430245[9].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's found in taxon is recorded as Valsa sordida[10].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's found in taxon is recorded as Cytospora chrysosperma[11].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's found in taxon is recorded as Papaver somniferum[12].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+271.120843404'}[13].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's SureChEMBL ID is recorded as 26388[14].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's UniChem compound ID is recorded as 1077985[15].
  • 7,8-didehydro-4,5-epoxymorphinan-3,6-diol's Probes And Drugs ID is recorded as PD093752[16].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Q2311683. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Phosphoproteomic and Metabolomic Profiling Uncovers the Roles of CcPmk1 in the Pathogenicity of Cytospora chrysosperma. wikidata.org.
  10. [11] ↑ . Phosphoproteomic and Metabolomic Profiling Uncovers the Roles of CcPmk1 in the Pathogenicity of Cytospora chrysosperma. wikidata.org.
  11. [12] ↑ . Chemiluminescence detection of opium poppy (Papaver somniferum) alkaloids. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . UniChem. wikidata.org.
  15. [16] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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