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(R)-1,2-distearoylphosphatidylethanolamine

chemical compound
ChemicalSubstance group_of_stereoisomers Q60533035
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Summary

(R)-1,2-distearoylphosphatidylethanolamine is a group of stereoisomers[1].

Key Facts

  • (R)-1,2-distearoylphosphatidylethanolamine's instance of is recorded as group of stereoisomers[2].
  • (R)-1,2-distearoylphosphatidylethanolamine's CAS Registry Number is recorded as 1069-79-0[3].
  • (R)-1,2-distearoylphosphatidylethanolamine's EC number is recorded as 213-963-9[4].
  • (R)-1,2-distearoylphosphatidylethanolamine's canonical SMILES is recorded as O=C(OCC(OC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OCCN)CCCCCCCCCCCCCCCCC[5].
  • (R)-1,2-distearoylphosphatidylethanolamine's InChI is recorded as InChI=1S/C41H82NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-40(43)47-37-39(38-49-51(45,46)48-36-35-42)50-41(44)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h39H,3-38,42H2,1-2H3,(H,45,46)/t39-/m1/s1[6].
  • (R)-1,2-distearoylphosphatidylethanolamine's InChIKey is recorded as LVNGJLRDBYCPGB-LDLOPFEMSA-N[7].
  • (R)-1,2-distearoylphosphatidylethanolamine's chemical formula is recorded as C₄₁H₈₂NO₈P[8].
  • (R)-1,2-distearoylphosphatidylethanolamine's subclass of is recorded as diacylglycerophosphoethanolamine[9].
  • (R)-1,2-distearoylphosphatidylethanolamine's UNII is recorded as 1G4B5265CQ[10].
  • (R)-1,2-distearoylphosphatidylethanolamine's PubChem CID is recorded as 447078[11].
  • (R)-1,2-distearoylphosphatidylethanolamine's PubChem CID is recorded as 15061530[12].
  • (R)-1,2-distearoylphosphatidylethanolamine's ChEBI ID is recorded as 47766[13].
  • (R)-1,2-distearoylphosphatidylethanolamine's ChEBI ID is recorded as 39934[14].
  • (R)-1,2-distearoylphosphatidylethanolamine's found in taxon is recorded as Streptomyces roseicoloratus[15].
  • (R)-1,2-distearoylphosphatidylethanolamine's found in taxon is recorded as Streptomyces sporangiiformans[16].
  • (R)-1,2-distearoylphosphatidylethanolamine's found in taxon is recorded as Hippophae rhamnoides[17].
  • (R)-1,2-distearoylphosphatidylethanolamine's Reaxys registry number is recorded as 1730641[18].
  • (R)-1,2-distearoylphosphatidylethanolamine's isomeric SMILES is recorded as CCCCCCCCCCCCCCCCCC(=O)OCC@HOC(=O)CCCCCCCCCCCCCCCCCC@HOC(=O)CCCCCCCCCCCCCCCCC">[19].
  • (R)-1,2-distearoylphosphatidylethanolamine's Human Metabolome Database ID is recorded as HMDB0008991[20].
  • (R)-1,2-distearoylphosphatidylethanolamine's LIPID MAPS ID is recorded as LMGP02010097[21].
  • (R)-1,2-distearoylphosphatidylethanolamine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+747.5778052139999'}[22].
  • (R)-1,2-distearoylphosphatidylethanolamine's ECHA Substance Infocard ID is recorded as 100.012.695[23].
  • (R)-1,2-distearoylphosphatidylethanolamine's SureChEMBL ID is recorded as 25605[24].
  • (R)-1,2-distearoylphosphatidylethanolamine's DSSTox substance ID is recorded as DTXSID601240990[25].
  • (R)-1,2-distearoylphosphatidylethanolamine's PDB ligand ID is recorded as PEH[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . CAS Common Chemistry. Retrieved . fdasis.nlm.nih.gov. Provenance: wikidata.org.
  3. [4] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . ChEBI release 2020-09-01. wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . PubChem. Retrieved . wikidata.org.
  12. [13] ↑ . ChEBI release 2019-10-02. wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . Characterization of Streptomyces sporangiiformans sp. nov., a Novel Soil Actinomycete with Antibacterial Activity against Ralstonia solanacearum. wikidata.org.
  15. [16] ↑ . Characterization of Streptomyces sporangiiformans sp. nov., a Novel Soil Actinomycete with Antibacterial Activity against Ralstonia solanacearum. wikidata.org.
  16. [17] ↑ . Hippophae rhamnoides L.: chromatographic methods to determine chemical composition, use in traditional medicine and pharmacological effects. wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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