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Sulfonoglycolipid

chemical compound
ChemicalSubstance group_of_stereoisomers Q42403295
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Sulfonoglycolipid

Summary

Sulfonoglycolipid is a group of stereoisomers[1].

Key Facts

  • Sulfonoglycolipid's instance of is recorded as group of stereoisomers[2].
  • Sulfonoglycolipid's CAS Registry Number is recorded as 109430-50-4[3].
  • Sulfonoglycolipid's canonical SMILES is recorded as O=C(OCC(OC(=O)CCCCCCCCCCCCCCC)COC1OC(CS(=O)(=O)O)C(O)C(O)C1O)CCCCCCCCCCCCCCC[4].
  • Sulfonoglycolipid's InChI is recorded as InChI=1S/C41H78O12S/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-36(42)50-31-34(32-51-41-40(46)39(45)38(44)35(53-41)33-54(47,48)49)52-37(43)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h34-35,38-41,44-46H,3-33H2,1-2H3,(H,47,48,49)/t34?,35-,38-,39+,40-,41+/m1/s1[5].
  • Sulfonoglycolipid's InChIKey is recorded as RVUUQPKXGDTQPG-PINKXYAGSA-N[6].
  • Sulfonoglycolipid's chemical formula is recorded as C₄₁H₇₈O₁₂S[7].
  • Sulfonoglycolipid's subclass of is recorded as chemical compound[8].
  • Sulfonoglycolipid's ChemSpider ID is recorded as 140119[9].
  • Sulfonoglycolipid's PubChem CID is recorded as 159321[10].
  • Sulfonoglycolipid's found in taxon is recorded as Aerva lanata[11].
  • Sulfonoglycolipid's isomeric SMILES is recorded as CCCCCCCCCCCCCCCC(=O)OCC(CO[C@H]1OC@HC@@HC@H[C@H]1O)OC(=O)CCCCCCCCCCCCCCCC@HC@@HC@H[C@H]1O)OC(=O)CCCCCCCCCCCCCCC">[12].
  • Sulfonoglycolipid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+794.5213989359997'}[13].
  • Sulfonoglycolipid's SureChEMBL ID is recorded as 6925719[14].
  • Sulfonoglycolipid's DSSTox substance ID is recorded as DTXSID40911161[15].
  • Sulfonoglycolipid's DSSTOX compound identifier is recorded as DTXCID901340200[16].
  • Sulfonoglycolipid's UniChem compound ID is recorded as 45649[17].

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] ↑ . wikidata.org.
  10. [11] ↑ . Isolation, structural elucidation and cytotoxicity evaluation of a new pentahydroxy-pimarane diterpenoid along with other chemical constituents from Aerva lanata.. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . 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). Sulfonoglycolipid. Retrieved May 3, 2026, from https://4ort.xyz/entity/sulfonoglycolipid
MLA “Sulfonoglycolipid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sulfonoglycolipid.
BibTeX @misc{4ortxyz_sulfonoglycolipid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Sulfonoglycolipid}}, year = {2026}, url = {https://4ort.xyz/entity/sulfonoglycolipid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Sulfonoglycolipid — https://4ort.xyz/entity/sulfonoglycolipid (retrieved 2026-05-03)

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