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vitetrifolin D

chemical compound
ChemicalSubstance group_of_stereoisomers Q27163172
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vitetrifolin D

Summary

vitetrifolin D is a group of stereoisomers[1].

Key Facts

  • vitetrifolin D's instance of is recorded as group of stereoisomers[2].
  • vitetrifolin D's CAS Registry Number is recorded as 351427-18-4[3].
  • vitetrifolin D's canonical SMILES is recorded as CC1C(C(C2=C(C1(C)CCC(C)(C=C)O)CCCC2(C)C)OC(=O)C)OC(=O)C[4].
  • vitetrifolin D's InChI is recorded as InChI=1S/C24H38O5/c1-9-23(7,27)13-14-24(8)15(2)20(28-16(3)25)21(29-17(4)26)19-18(24)11-10-12-22(19,5)6/h9,15,20-21,27H,1,10-14H2,2-8H3/t15-,20-,21+,23?,24-/m1/s1[5].
  • vitetrifolin D's InChIKey is recorded as JSGVRMXIAILPPO-FWPWNEHFSA-N[6].
  • vitetrifolin D's chemical formula is recorded as C₂₄H₃₈O₅[7].
  • vitetrifolin D's subclass of is recorded as chemical compound[8].
  • vitetrifolin D's ChEMBL ID is recorded as CHEMBL2436600[9].
  • vitetrifolin D's ChemSpider ID is recorded as 9190201[10].
  • vitetrifolin D's PubChem CID is recorded as 11015016[11].
  • vitetrifolin D's ChEBI ID is recorded as 91266[12].
  • vitetrifolin D's found in taxon is recorded as Vitex trifolia[13].
  • vitetrifolin D's found in taxon is recorded as Vitex negundo[14].
  • vitetrifolin D's Reaxys registry number is recorded as 9160882[15].
  • vitetrifolin D's isomeric SMILES is recorded as C[C@@H]1C@HOC(=O)CC@HOC(=O)C">[16].
  • vitetrifolin D's KNApSAcK ID is recorded as C00033484[17].
  • vitetrifolin D's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+406.271924'}[18].
  • vitetrifolin D's SureChEMBL ID is recorded as 29801483[19].
  • vitetrifolin D's DSSTox substance ID is recorded as DTXSID701317269[20].
  • vitetrifolin D's UniChem compound ID is recorded as 32830180[21].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: 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] ↑ . Labdane-type diterpenes as new cell cycle inhibitors and apoptosis inducers from Vitex trifolia L. wikidata.org.
  13. [14] ↑ . Hh signaling inhibitors from Vitex negundo; naturally occurring inhibitors of the GLI1–DNA complex. wikidata.org.
  14. [15] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [16] ↑ . PubChem. Retrieved . wikidata.org.
  16. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [18] ↑ . PubChem. Retrieved . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . 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). vitetrifolin D. Retrieved May 3, 2026, from https://4ort.xyz/entity/vitetrifolin-d
MLA “vitetrifolin D.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vitetrifolin-d.
BibTeX @misc{4ortxyz_vitetrifolin-d_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vitetrifolin D}}, year = {2026}, url = {https://4ort.xyz/entity/vitetrifolin-d}, note = {Accessed: 2026-05-03}}
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