shikalkin

group of stereoisomers with the chemical formula C₁₆H₁₆O₅
ChemicalSubstance group_of_stereoisomers Q105178326
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shikalkin

Summary

shikalkin is a group of stereoisomers[1].

Key Facts

  • shikalkin's instance of is recorded as group of stereoisomers[2].
  • shikalkin's chemical structure is recorded as Shikalkin.svg[3].
  • shikalkin's canonical SMILES is recorded as O=C1C=C(C(=O)C=2C(O)=CC=C(O)C12)C(O)CC=C(C)C[4].
  • shikalkin's InChI is recorded as InChI=1S/C16H16O5/c1-8(2)3-4-10(17)9-7-13(20)14-11(18)5-6-12(19)15(14)16(9)21/h3,5-7,10,17-19H,4H2,1-2H3[5].
  • shikalkin's InChIKey is recorded as NEZONWMXZKDMKF-UHFFFAOYSA-N[6].
  • shikalkin's chemical formula is recorded as C₁₆H₁₆O₅[7].
  • shikalkin's subclass of is recorded as 2,6-dimethyloctane monoterpenoid[8].
  • shikalkin's subclass of is recorded as biogenic naphthochinone[9].
  • shikalkin's PubChem CID is recorded as 5208[10].
  • shikalkin's ChEBI ID is recorded as 174748[11].
  • shikalkin's found in taxon is recorded as Boraginaceae[12].
  • shikalkin's found in taxon is recorded as Arnebia guttata[13].
  • shikalkin's found in taxon is recorded as Lithospermum erythrorhizon[14].
  • shikalkin's found in taxon is recorded as Lithospermum officinale[15].
  • shikalkin's found in taxon is recorded as Arnebia decumbens[16].
  • shikalkin's Human Metabolome Database ID is recorded as HMDB0030579[17].
  • shikalkin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+288.099773612'}[18].
  • shikalkin's SureChEMBL ID is recorded as 3182028[19].
  • shikalkin's SureChEMBL ID is recorded as 29410804[20].
  • shikalkin's NMRShiftDB structure ID is recorded as 20167676[21].
  • shikalkin's UniChem compound ID is recorded as 22739265[22].
  • shikalkin's Probes And Drugs ID is recorded as PD038819[23].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . PubChem. Retrieved . wikidata.org.
  10. [11] . ChEBI release 2022-06-13. wikidata.org.
  11. [12] . Shikonin exerts anti-inflammatory effects in a murine model of lipopolysaccharide-induced acute lung injury by inhibiting the nuclear factor-kappaB signaling pathway. wikidata.org.
  12. [13] . Antimicrobial activities of naphthazarins from Arnebia euchroma. wikidata.org.
  13. [14] . Naphthoquinones ofLithospermum erythrorhizon. wikidata.org.
  14. [15] . Geranylpyrophosphate synthase from cell cultures of Lithospermum erythrorhizon. wikidata.org.
  15. [16] . Shikonin Derivatives, Part VI. Chemical Investigations of Arnebia decumbens. wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . UniChem. wikidata.org.
  22. [23] . 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). shikalkin. Retrieved May 3, 2026, from https://4ort.xyz/entity/shikalkin
MLA “shikalkin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/shikalkin.
BibTeX @misc{4ortxyz_shikalkin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{shikalkin}}, year = {2026}, url = {https://4ort.xyz/entity/shikalkin}, note = {Accessed: 2026-05-03}}
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