Clavamycin E

chemical compound
ChemicalSubstance group_of_stereoisomers Q27154993
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Clavamycin E

Summary

Clavamycin E is a group of stereoisomers[1].

Key Facts

  • Clavamycin E's instance of is recorded as group of stereoisomers[2].
  • Clavamycin E's canonical SMILES is recorded as CC(C(=O)NC(C(C1CN2C(O1)CC2=O)O)C(=O)O)N[3].
  • Clavamycin E's InChI is recorded as InChI=1S/C11H17N3O6/c1-4(12)10(17)13-8(11(18)19)9(16)5-3-14-6(15)2-7(14)20-5/h4-5,7-9,16H,2-3,12H2,1H3,(H,13,17)(H,18,19)/t4-,5+,7-,8-,9?/m0/s1[4].
  • Clavamycin E's InChIKey is recorded as HYVUCUGHACXFFU-NQIQCGANSA-N[5].
  • Clavamycin E's chemical formula is recorded as C₁₁H₁₇N₃O₆[6].
  • Clavamycin E's subclass of is recorded as (2S)-2-[[(2S)-2-aminopropanoyl]amino]-3-hydroxy-3-[(3R)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptan-3-yl]propanoic acid[7].
  • Clavamycin E's ChemSpider ID is recorded as 30791679[8].
  • Clavamycin E's PubChem CID is recorded as 46173893[9].
  • Clavamycin E's KEGG ID is recorded as C17365[10].
  • Clavamycin E's ChEBI ID is recorded as 81034[11].
  • Clavamycin E's found in taxon is recorded as Streptomyces hygroscopicus[12].
  • Clavamycin E's isomeric SMILES is recorded as CC@@HNC@@HN">[13].
  • Clavamycin E's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+287.111735'}[14].
  • Clavamycin E's SureChEMBL ID is recorded as 29884645[15].
  • Clavamycin E's UniChem compound ID is recorded as 1073215[16].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . PubChem. Retrieved . wikidata.org.
  3. [4] . PubChem. Retrieved . wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . Q2311683. Retrieved . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . ChEBI. Retrieved . wikidata.org.
  10. [11] . ChEBI. Retrieved . wikidata.org.
  11. [12] . Q105035489. wikidata.org.
  12. [13] . PubChem. Retrieved . wikidata.org.
  13. [14] . PubChem. Retrieved . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . UniChem. 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). Clavamycin E. Retrieved May 3, 2026, from https://4ort.xyz/entity/clavamycin-e
MLA “Clavamycin E.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/clavamycin-e.
BibTeX @misc{4ortxyz_clavamycin-e_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Clavamycin E}}, year = {2026}, url = {https://4ort.xyz/entity/clavamycin-e}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Clavamycin E — https://4ort.xyz/entity/clavamycin-e (retrieved 2026-05-03)

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