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hyponine E

chemical compound
ChemicalSubstance group_of_stereoisomers Q27225553
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hyponine E

Summary

hyponine E is a group of stereoisomers[1].

Key Facts

  • hyponine E's instance of is recorded as group of stereoisomers[2].
  • hyponine E's CAS Registry Number is recorded as 226975-99-1[3].
  • hyponine E's canonical SMILES is recorded as CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C6=CC=CO6)OC(=O)C7=CN=CC=C7)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C[4].
  • hyponine E's InChI is recorded as InChI=1S/C45H48N2O19/c1-21-22(2)38(52)65-35-33(60-24(4)49)37(62-26(6)51)44(20-58-23(3)48)36(61-25(5)50)32(63-39(53)27-12-9-15-46-18-27)30-34(64-41(55)29-14-11-17-57-29)45(44,43(35,8)56)66-42(30,7)19-59-40(54)28-13-10-16-47-31(21)28/h9-18,21-22,30,32-37,56H,19-20H2,1-8H3/t21?,22?,30-,32-,33+,34-,35+,36-,37+,42+,43+,44-,45+/m1/s1[5].
  • hyponine E's InChIKey is recorded as PMRSIAJYXABCTQ-IWYQQVOHSA-N[6].
  • hyponine E's chemical formula is recorded as C₄₅H₄₈N₂O₁₉[7].
  • hyponine E's subclass of is recorded as chemical compound[8].
  • hyponine E's ChEMBL ID is recorded as CHEMBL501685[9].
  • hyponine E's ChemSpider ID is recorded as 24710294[10].
  • hyponine E's PubChem CID is recorded as 44583772[11].
  • hyponine E's ChEBI ID is recorded as 132389[12].
  • hyponine E's isomeric SMILES is recorded as CC1C(C(=O)O[C@H]2C@@HOC(=O)C)CC@@H">[13].
  • hyponine E's KNApSAcK ID is recorded as C00039396[14].
  • hyponine E's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+920.285'}[15].
  • hyponine E's SureChEMBL ID is recorded as 31441809[16].
  • hyponine E's UniChem compound ID is recorded as 244186[17].

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] ↑ . ChEMBL. Retrieved . wikidata.org.
  9. [10] ↑ . Q2311683. Retrieved . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . ChEBI. Retrieved . wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . 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). hyponine E. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyponine-e
MLA “hyponine E.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyponine-e.
BibTeX @misc{4ortxyz_hyponine-e_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyponine E}}, year = {2026}, url = {https://4ort.xyz/entity/hyponine-e}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hyponine E — https://4ort.xyz/entity/hyponine-e (retrieved 2026-05-03)

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