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hyponine D

chemical compound
ChemicalSubstance group_of_stereoisomers Q27225552
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hyponine D

Summary

hyponine D is a group of stereoisomers[1].

Key Facts

  • hyponine D's instance of is recorded as group of stereoisomers[2].
  • hyponine D's CAS Registry Number is recorded as 259823-31-9[3].
  • hyponine D'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=CC=C6)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C7=CN=CC=C7)C[4].
  • hyponine D's InChI is recorded as InChI=1S/C47H50N2O18/c1-23-24(2)40(54)66-37-35(64-42(56)30-16-12-18-48-20-30)39(63-28(6)53)46(22-59-25(3)50)38(62-27(5)52)34(61-26(4)51)32-36(65-41(55)29-14-10-9-11-15-29)47(46,45(37,8)58)67-44(32,7)21-60-43(57)31-17-13-19-49-33(23)31/h9-20,23-24,32,34-39,58H,21-22H2,1-8H3/t23?,24?,32-,34-,35+,36-,37+,38-,39+,44+,45+,46-,47+/m1/s1[5].
  • hyponine D's InChIKey is recorded as BDKQPFFHSCFTQW-UWRKWEHLSA-N[6].
  • hyponine D's chemical formula is recorded as C₄₇H₅₀N₂O₁₈[7].
  • hyponine D's subclass of is recorded as eudesmane sesquiterpenoid[8].
  • hyponine D's subclass of is recorded as pyridine alkaloid[9].
  • hyponine D's subclass of is recorded as macrolides[10].
  • hyponine D's ChEMBL ID is recorded as CHEMBL504037[11].
  • hyponine D's ChemSpider ID is recorded as 24710745[12].
  • hyponine D's PubChem CID is recorded as 44593669[13].
  • hyponine D's ChEBI ID is recorded as 132388[14].
  • hyponine D's found in taxon is recorded as Tripterygium wilfordii[15].
  • hyponine D's Reaxys registry number is recorded as 8671241[16].
  • hyponine D's isomeric SMILES is recorded as CC1C(C(=O)O[C@H]2C@@HOC(=O)C7=CN=CC=C7)CC@@H">[17].
  • hyponine D's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+930.306'}[18].
  • hyponine D's SureChEMBL ID is recorded as 29725329[19].
  • hyponine D's UniChem compound ID is recorded as 245471[20].

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] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [12] ↑ . Q2311683. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . ChEBI. Retrieved . wikidata.org.
  14. [15] ↑ . Tripfordines A-C, sesquiterpene pyridine alkaloids from Tripterygium wilfordii, and structure anti-HIV activity relationships of Tripterygium alkaloids. wikidata.org.
  15. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [17] ↑ . PubChem. Retrieved . wikidata.org.
  17. [18] ↑ . PubChem. Retrieved . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . 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). hyponine D. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyponine-d
MLA “hyponine D.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyponine-d.
BibTeX @misc{4ortxyz_hyponine-d_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyponine D}}, year = {2026}, url = {https://4ort.xyz/entity/hyponine-d}, note = {Accessed: 2026-05-03}}
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