(R)-edelfosine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27147892
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(R)-edelfosine

Summary

(R)-edelfosine is a group of stereoisomers[1].

Key Facts

  • (R)-edelfosine's instance of is recorded as group of stereoisomers[2].
  • (R)-edelfosine's CAS Registry Number is recorded as 70641-51-9[3].
  • (R)-edelfosine's canonical SMILES is recorded as CCCCCCCCCCCCCCCCCCOCC(COP(=O)([O-])OCCN+(C)C)OCN+(C)C)OC">[4].
  • (R)-edelfosine's InChI is recorded as InChI=1S/C27H58NO6P/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-23-32-25-27(31-5)26-34-35(29,30)33-24-22-28(2,3)4/h27H,6-26H2,1-5H3/t27-/m1/s1[5].
  • (R)-edelfosine's InChIKey is recorded as MHFRGQHAERHWKZ-HHHXNRCGSA-N[6].
  • (R)-edelfosine's chemical formula is recorded as C₂₇H₅₈NO₆P[7].
  • (R)-edelfosine's subclass of is recorded as chemical compound[8].
  • (R)-edelfosine's ChEMBL ID is recorded as CHEMBL107514[9].
  • (R)-edelfosine's UNII is recorded as LZ198HY9OE[10].
  • (R)-edelfosine's ChemSpider ID is recorded as 5293425[11].
  • (R)-edelfosine's PubChem CID is recorded as 6918215[12].
  • (R)-edelfosine's ChEBI ID is recorded as 78653[13].
  • (R)-edelfosine's Reaxys registry number is recorded as 6376409[14].
  • (R)-edelfosine's isomeric SMILES is recorded as CCCCCCCCCCCCCCCCCCOCC@HOCC@HOC">[15].
  • (R)-edelfosine's LIPID MAPS ID is recorded as LMGP01040048[16].
  • (R)-edelfosine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+523.4'}[17].
  • (R)-edelfosine's SureChEMBL ID is recorded as 436257[18].
  • (R)-edelfosine's DSSTox substance ID is recorded as DTXSID9045766[19].
  • (R)-edelfosine's DSSTox substance ID is recorded as DTXSID20922896[20].
  • (R)-edelfosine's DSSTOX compound identifier is recorded as DTXCID7025766[21].
  • (R)-edelfosine's UniChem compound ID is recorded as 430398[22].
  • (R)-edelfosine's Probes And Drugs ID is recorded as PD015379[23].

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] . PubChem. Retrieved . wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . PubChem. Retrieved . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . ChEMBL. Retrieved . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . Q2311683. Retrieved . wikidata.org.
  11. [12] . PubChem. Retrieved . wikidata.org.
  12. [13] . ChEBI. Retrieved . wikidata.org.
  13. [14] . ChEBI. Retrieved . wikidata.org.
  14. [15] . PubChem. Retrieved . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . PubChem. Retrieved . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . UniChem. wikidata.org.
  22. [23] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). (R)-edelfosine. Retrieved May 3, 2026, from https://4ort.xyz/entity/-r-edelfosine
MLA “(R)-edelfosine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-r-edelfosine.
BibTeX @misc{4ortxyz_-r-edelfosine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(R)-edelfosine}}, year = {2026}, url = {https://4ort.xyz/entity/-r-edelfosine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (R)-edelfosine — https://4ort.xyz/entity/-r-edelfosine (retrieved 2026-05-03)

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