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halistanol sulfonic acid F

chemical compound
ChemicalSubstance group_of_stereoisomers Q27139950
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Summary

halistanol sulfonic acid F is a group of stereoisomers[1].

Key Facts

  • halistanol sulfonic acid F's instance of is recorded as group of stereoisomers[2].
  • halistanol sulfonic acid F's canonical SMILES is recorded as CCC(C)(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4C3(CC(C(C4)OS(=O)(=O)O)OS(=O)(=O)O)C)OS(=O)(=O)O)C[3].
  • halistanol sulfonic acid F's InChI is recorded as InChI=1S/C30H54O12S3/c1-8-28(4,5)19(3)10-9-18(2)21-11-12-22-20-15-25(40-43(31,32)33)24-16-26(41-44(34,35)36)27(42-45(37,38)39)17-30(24,7)23(20)13-14-29(21,22)6/h18-27H,8-17H2,1-7H3,(H,31,32,33)(H,34,35,36)(H,37,38,39)/t18-,19?,20+,21-,22+,23+,24-,25+,26+,27+,29-,30-/m1/s1[4].
  • halistanol sulfonic acid F's InChIKey is recorded as XUMJIMYIZJLITA-TZVJEUQOSA-N[5].
  • halistanol sulfonic acid F's chemical formula is recorded as C₃₀H₅₄O₁₂S₃[6].
  • halistanol sulfonic acid F's subclass of is recorded as sterol[7].
  • halistanol sulfonic acid F's subclass of is recorded as [(2S,3S,5S,6S,10R,13R,17R)-10,13-dimethyl-2,3-disulfooxy-17-[(1R)-1,4,5,5-tetramethylheptyl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl] hydrogen sulfate[8].
  • halistanol sulfonic acid F's ChEMBL ID is recorded as CHEMBL1208164[9].
  • halistanol sulfonic acid F's ChemSpider ID is recorded as 25056339[10].
  • halistanol sulfonic acid F's PubChem CID is recorded as 44575671[11].
  • halistanol sulfonic acid F's ChEBI ID is recorded as 72477[12].
  • halistanol sulfonic acid F's found in taxon is recorded as Axinyssa digitata[13].
  • halistanol sulfonic acid F's isomeric SMILES is recorded as CCC(C)(C)C(C)CCC@@H[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC@@HOS(=O)(=O)O)CC@@H[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC@@HOS(=O)(=O)O)C">[14].
  • halistanol sulfonic acid F's LIPID MAPS ID is recorded as LMST05020036[15].
  • halistanol sulfonic acid F's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+702.27774'}[16].
  • halistanol sulfonic acid F's UniChem compound ID is recorded as 638616[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] ↑ . wikidata.org.
  8. [9] ↑ . ChEMBL. Retrieved . wikidata.org.
  9. [10] ↑ . ChemSpider. Retrieved . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . Novel HIV-inhibitory halistanol sulfates F-H from a marine sponge, Pseudoaxinissa digitata. wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  15. [16] ↑ . PubChem. Retrieved . wikidata.org.
  16. [17] ↑ . 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). halistanol sulfonic acid F. Retrieved May 3, 2026, from https://4ort.xyz/entity/halistanol-sulfonic-acid-f
MLA “halistanol sulfonic acid F.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/halistanol-sulfonic-acid-f.
BibTeX @misc{4ortxyz_halistanol-sulfonic-acid-f_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{halistanol sulfonic acid F}}, year = {2026}, url = {https://4ort.xyz/entity/halistanol-sulfonic-acid-f}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): halistanol sulfonic acid F — https://4ort.xyz/entity/halistanol-sulfonic-acid-f (retrieved 2026-05-03)

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