(RS)-eflornithine

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q424751
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(RS)-eflornithine

Summary

(RS)-eflornithine is a group of stereoisomers[1]. (RS)-eflornithine draws 105 Wikipedia views per month (group_of_stereoisomers category, ranking #143 of 1,063).[2]

Key Facts

  • (RS)-eflornithine's instance of is recorded as group of stereoisomers[3].
  • (RS)-eflornithine's chemical structure is recorded as (±)-Eflornithin Structural Formulae V.1.svg[4].
  • (RS)-eflornithine's chemical structure is recorded as Eflornithine.svg[5].
  • (RS)-eflornithine's physically interacts with is recorded as Ornithine decarboxylase 1[6].
  • (RS)-eflornithine's CAS Registry Number is recorded as 70052-12-9[7].
  • (RS)-eflornithine's canonical SMILES is recorded as C(CC(C(F)F)(C(=O)O)N)CN[8].
  • (RS)-eflornithine's InChI is recorded as InChI=1S/C6H12F2N2O2/c7-4(8)6(10,5(11)12)2-1-3-9/h4H,1-3,9-10H2,(H,11,12)[9].
  • (RS)-eflornithine's InChIKey is recorded as VLCYCQAOQCDTCN-UHFFFAOYSA-N[10].
  • (RS)-eflornithine's ATC code is recorded as P01CX03[11].
  • (RS)-eflornithine's ATC code is recorded as D11AX16[12].
  • (RS)-eflornithine's chemical formula is recorded as C₆H₁₂F₂N₂O₂[13].
  • (RS)-eflornithine's subclass of is recorded as bactericide[14].
  • (RS)-eflornithine's Commons category is recorded as Eflornithine[15].
  • (RS)-eflornithine's MeSH descriptor ID is recorded as D000518[16].
  • (RS)-eflornithine's ChEMBL ID is recorded as CHEMBL830[17].
  • (RS)-eflornithine's Guide to Pharmacology Ligand ID is recorded as 5176[18].
  • (RS)-eflornithine's Freebase ID is recorded as /m/052ssm[19].
  • (RS)-eflornithine's UNII is recorded as ZQN1G5V6SR[20].
  • (RS)-eflornithine's ChemSpider ID is recorded as 2902[21].
  • (RS)-eflornithine's PubChem CID is recorded as 3009[22].
  • (RS)-eflornithine's KEGG ID is recorded as D07883[23].
  • (RS)-eflornithine's MeSH tree code is recorded as D12.125.068.665.340[24].
  • (RS)-eflornithine's MeSH tree code is recorded as D12.125.095.765.340[25].
  • (RS)-eflornithine's ChEBI ID is recorded as 41948[26].
  • (RS)-eflornithine's DrugBank ID is recorded as DB06243[27].

Why It Matters

(RS)-eflornithine draws 105 Wikipedia views per month (group_of_stereoisomers category, ranking #143 of 1,063).[2] (RS)-eflornithine has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[28] (RS)-eflornithine is known by 16 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . DrugBank. wikidata.org.
  10. [12] . DrugBank. wikidata.org.
  11. [13] . PubChem. Retrieved . wikidata.org.
  12. [14] . ChEBI. wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . ChEMBL. Retrieved . wikidata.org.
  16. [18] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] . Freebase Data Dumps. wikidata.org.
  18. [20] . Global Substance Registration System. Retrieved . wikidata.org.
  19. [21] . Q2311683. Retrieved . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . ChEBI. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . ChEMBL. Retrieved . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . Wikidata aliases. wikidata.org.

📑 Cite this page

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). (RS)-eflornithine. Retrieved May 3, 2026, from https://4ort.xyz/entity/rs-eflornithine
MLA “(RS)-eflornithine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rs-eflornithine.
BibTeX @misc{4ortxyz_rs-eflornithine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(RS)-eflornithine}}, year = {2026}, url = {https://4ort.xyz/entity/rs-eflornithine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (RS)-eflornithine — https://4ort.xyz/entity/rs-eflornithine (retrieved 2026-05-03)

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