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Parishin B

chemical compound
ChemicalSubstance group_of_stereoisomers Q27155063
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Parishin B

Summary

Parishin B is a group of stereoisomers[1].

Key Facts

  • Parishin B's instance of is recorded as group of stereoisomers[2].
  • Parishin B's canonical SMILES is recorded as C1=CC(=CC=C1COC(=O)CC(CC(=O)O)(C(=O)OCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O[3].
  • Parishin B's InChI is recorded as InChI=1S/C32H40O19/c33-11-19-23(38)25(40)27(42)29(50-19)48-17-5-1-15(2-6-17)13-46-22(37)10-32(45,9-21(35)36)31(44)47-14-16-3-7-18(8-4-16)49-30-28(43)26(41)24(39)20(12-34)51-30/h1-8,19-20,23-30,33-34,38-43,45H,9-14H2,(H,35,36)/t19-,20-,23-,24-,25+,26+,27-,28-,29-,30-,32?/m1/s1[4].
  • Parishin B's InChIKey is recorded as UNLDMOJTKKEMOG-IWOWLDPGSA-N[5].
  • Parishin B's chemical formula is recorded as C₃₂H₄₀O₁₉[6].
  • Parishin B's subclass of is recorded as chemical compound[7].
  • Parishin B's ChemSpider ID is recorded as 23551088[8].
  • Parishin B's PubChem CID is recorded as 44715528[9].
  • Parishin B's KEGG ID is recorded as C17465[10].
  • Parishin B's ChEBI ID is recorded as 81108[11].
  • Parishin B's found in taxon is recorded as Artemisia absinthium[12].
  • Parishin B's isomeric SMILES is recorded as C1=CC(=CC=C1COC(=O)CC(CC(=O)O)(C(=O)OCC2=CC=C(C=C2)O[C@H]3C@@HO)O)O[C@H]4C@@HOC@@HO)O)O[C@H]4C@@HO">[13].
  • Parishin B's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+728.216'}[14].
  • Parishin B's SureChEMBL ID is recorded as 29392493[15].
  • Parishin B's UniChem compound ID is recorded as 1069386[16].
  • Parishin B's Probes And Drugs ID is recorded as PD088041[17].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Q2311683. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . ChEBI. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Sesquiterpene lactones of two species of Artemisia. wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.
  16. [17] ↑ . 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). Parishin B. Retrieved May 3, 2026, from https://4ort.xyz/entity/parishin-b
MLA “Parishin B.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/parishin-b.
BibTeX @misc{4ortxyz_parishin-b_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Parishin B}}, year = {2026}, url = {https://4ort.xyz/entity/parishin-b}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Parishin B — https://4ort.xyz/entity/parishin-b (retrieved 2026-05-03)

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