2,6-diaminopimelic acid

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q30126674
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2,6-diaminopimelic acid

Summary

2,6-diaminopimelic acid is a group of stereoisomers[1]. It draws 10 Wikipedia views per month (group_of_stereoisomers category, ranking #208 of 1,063).[2]

Key Facts

  • 2,6-diaminopimelic acid's instance of is recorded as group of stereoisomers[3].
  • 2,6-diaminopimelic acid's chemical structure is recorded as 2,6-diaminoheptanedioic acid 200.svg[4].
  • 2,6-diaminopimelic acid's CAS Registry Number is recorded as 583-93-7[5].
  • 2,6-diaminopimelic acid's EC number is recorded as 209-524-6[6].
  • 2,6-diaminopimelic acid's canonical SMILES is recorded as C(CC(C(=O)O)N)CC(C(=O)O)N[7].
  • 2,6-diaminopimelic acid's InChI is recorded as InChI=1S/C7H14N2O4/c8-4(6(10)11)2-1-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)[8].
  • 2,6-diaminopimelic acid's InChIKey is recorded as GMKMEZVLHJARHF-UHFFFAOYSA-N[9].
  • 2,6-diaminopimelic acid's chemical formula is recorded as C₇H₁₄N₂O₄[10].
  • 2,6-diaminopimelic acid's subclass of is recorded as dicarboxylic acid[11].
  • 2,6-diaminopimelic acid's subclass of is recorded as primary amine[12].
  • 2,6-diaminopimelic acid's subclass of is recorded as diamino acid[13].
  • 2,6-diaminopimelic acid's part of is recorded as diaminopimelate transport[14].
  • 2,6-diaminopimelic acid's Commons category is recorded as 2,6-Diaminopimelic acid[15].
  • 2,6-diaminopimelic acid's Freebase ID is recorded as /m/04qbjs6[16].
  • 2,6-diaminopimelic acid's ChemSpider ID is recorded as 842[17].
  • 2,6-diaminopimelic acid's PubChem CID is recorded as 865[18].
  • 2,6-diaminopimelic acid's PubChem CID is recorded as 53448507[19].
  • 2,6-diaminopimelic acid's ChEBI ID is recorded as 23673[20].
  • 2,6-diaminopimelic acid's found in taxon is recorded as Phaseolus vulgaris[21].
  • 2,6-diaminopimelic acid's found in taxon is recorded as soybean[22].
  • 2,6-diaminopimelic acid's Human Metabolome Database ID is recorded as HMDB0242532[23].
  • 2,6-diaminopimelic acid's KNApSAcK ID is recorded as C00062306[24].
  • 2,6-diaminopimelic acid's KNApSAcK ID is recorded as C00063386[25].
  • 2,6-diaminopimelic acid's mass is recorded as {'unit': 'Q483261', 'amount': '+190.095356928'}[26].
  • 2,6-diaminopimelic acid's ECHA Substance Infocard ID is recorded as 100.008.660[27].

Why It Matters

2,6-diaminopimelic acid draws 10 Wikipedia views per month (group_of_stereoisomers category, ranking #208 of 1,063).[2] It has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[28] It is known by 5 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] . ChemIDplus. Retrieved . chem.nlm.nih.gov. Provenance: wikidata.org.
  4. [6] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . ChemIDplus. Retrieved . chem.nlm.nih.gov. Provenance: wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Gene Ontology release 2019-11-16. wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . Metabolite Profiling of Root Exudates of Common Bean under Phosphorus Deficiency. wikidata.org.
  20. [22] . Metabolite profiling of soybean root exudates under phosphorus deficiency. wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . ECHA Substance Infocard database. Retrieved . 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). 2,6-diaminopimelic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-6-diaminopimelic-acid
MLA “2,6-diaminopimelic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2-6-diaminopimelic-acid.
BibTeX @misc{4ortxyz_2-6-diaminopimelic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2,6-diaminopimelic acid}}, year = {2026}, url = {https://4ort.xyz/entity/2-6-diaminopimelic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 2,6-diaminopimelic acid — https://4ort.xyz/entity/2-6-diaminopimelic-acid (retrieved 2026-05-03)

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