staphyloferrin A

chemical compound
ChemicalSubstance group_of_stereoisomers Q27158010
Press Enter · cited answer in seconds

staphyloferrin A

Summary

staphyloferrin An is a group of stereoisomers[1].

Key Facts

  • staphyloferrin A's instance of is recorded as group of stereoisomers[2].
  • staphyloferrin A's CAS Registry Number is recorded as 127902-98-1[3].
  • staphyloferrin A's canonical SMILES is recorded as C(CC(C(=O)O)NC(=O)CC(CC(=O)O)(C(=O)O)O)CNC(=O)CC(CC(=O)O)(C(=O)O)O[4].
  • staphyloferrin A's InChI is recorded as InChI=1S/C17H24N2O14/c20-9(4-16(32,14(28)29)6-11(22)23)18-3-1-2-8(13(26)27)19-10(21)5-17(33,15(30)31)7-12(24)25/h8,32-33H,1-7H2,(H,18,20)(H,19,21)(H,22,23)(H,24,25)(H,26,27)(H,28,29)(H,30,31)/t8-,16?,17?/m1/s1[5].
  • staphyloferrin A's InChIKey is recorded as VJSIXUQLTJCRCS-PJPOUAMNSA-N[6].
  • staphyloferrin A's chemical formula is recorded as C₁₇H₂₄N₂O₁₄[7].
  • staphyloferrin A's subclass of is recorded as chemical compound[8].
  • staphyloferrin A's ChemSpider ID is recorded as 34449072[9].
  • staphyloferrin A's PubChem CID is recorded as 46926095[10].
  • staphyloferrin A's ChEBI ID is recorded as 84711[11].
  • staphyloferrin A's Reaxys registry number is recorded as 26649296[12].
  • staphyloferrin A's isomeric SMILES is recorded as C(CC@HNC(=O)CC(CC(=O)O)(C(=O)O)O)CNC(=O)CC(CC(=O)O)(C(=O)O)OC@HNC(=O)CC(CC(=O)O)(C(=O)O)O)CNC(=O)CC(CC(=O)O)(C(=O)O)O">[13].
  • staphyloferrin A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+480.123'}[14].
  • staphyloferrin A's DSSTox substance ID is recorded as DTXSID10926020[15].
  • staphyloferrin A's Natural Product Atlas ID is recorded as NPA024679[16].
  • staphyloferrin A's DSSTOX compound identifier is recorded as DTXCID201354840[17].
  • staphyloferrin A's UniChem compound ID is recorded as 57077166[18].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . ChEBI. Retrieved . 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] ↑ . Q2311683. Retrieved . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). staphyloferrin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/staphyloferrin-a-q27158010
MLA “staphyloferrin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/staphyloferrin-a-q27158010.
BibTeX @misc{4ortxyz_staphyloferrin-a-q27158010_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{staphyloferrin A}}, year = {2026}, url = {https://4ort.xyz/entity/staphyloferrin-a-q27158010}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): staphyloferrin A — https://4ort.xyz/entity/staphyloferrin-a-q27158010 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/staphyloferrin-a-q27158010 · Last refreshed: