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PC(P-16:0/18:1(11Z))

chemical compound
ChemicalSubstance group_of_stereoisomers Q27162223
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Summary

PC(P-16:0/18:1(11Z)) is a group of stereoisomers[1].

Key Facts

  • PC(P-16:0/18:1(11Z))'s instance of is recorded as group of stereoisomers[2].
  • PC(P-16:0/18:1(11Z))'s canonical SMILES is recorded as CCCCCCCCCCCCCCC=COCC(COP(=O)([O-])OCCN+(C)C)OC(=O)CCCCCCCCCC=CCCCCCCN+(C)C)OC(=O)CCCCCCCCCC=CCCCCCC">[3].
  • PC(P-16:0/18:1(11Z))'s InChI is recorded as InChI=1S/C42H82NO7P/c1-6-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-42(44)50-41(40-49-51(45,46)48-38-36-43(3,4)5)39-47-37-34-32-30-28-26-24-21-19-17-15-13-11-9-7-2/h16,18,34,37,41H,6-15,17,19-33,35-36,38-40H2,1-5H3/b18-16-,37-34-/t41-/m1/s1[4].
  • PC(P-16:0/18:1(11Z))'s InChIKey is recorded as MVDFTRYOOPZXII-JEPFLRBFSA-N[5].
  • PC(P-16:0/18:1(11Z))'s chemical formula is recorded as C₄₂H₈₂NO₇P[6].
  • PC(P-16:0/18:1(11Z))'s subclass of is recorded as 1-(1Z-alkenyl),2-acylglycerophosphocholines[7].
  • PC(P-16:0/18:1(11Z))'s ChemSpider ID is recorded as 24767484[8].
  • PC(P-16:0/18:1(11Z))'s PubChem CID is recorded as 53480679[9].
  • PC(P-16:0/18:1(11Z))'s ChEBI ID is recorded as 89999[10].
  • PC(P-16:0/18:1(11Z))'s isomeric SMILES is recorded as CCCCCCCCCCCCCC/C=C\OCC@HOC(=O)CCCCCCCCC/C=C\CCCCCCC@HOC(=O)CCCCCCCCC/C=C\CCCCCC">[11].
  • PC(P-16:0/18:1(11Z))'s Human Metabolome Database ID is recorded as HMDB0011209[12].
  • PC(P-16:0/18:1(11Z))'s LIPID MAPS ID is recorded as LMGP01030128[13].
  • PC(P-16:0/18:1(11Z))'s mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+743.583'}[14].
  • PC(P-16:0/18:1(11Z))'s SureChEMBL ID is recorded as 30653070[15].
  • PC(P-16:0/18:1(11Z))'s SwissLipids ID is recorded as SLM:000048858[16].
  • PC(P-16:0/18:1(11Z))'s UniChem compound ID is recorded as 31995108[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] ↑ . ChemSpider. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . ChEBI. Retrieved . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . SwissLipids. Retrieved . swisslipids.org. Provenance: wikidata.org.
  16. [17] ↑ . UniChem. 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). PC(P-16:0/18:1(11Z)). Retrieved May 3, 2026, from https://4ort.xyz/entity/pc-p-16-0-18-1-11z-
MLA “PC(P-16:0/18:1(11Z)).” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/pc-p-16-0-18-1-11z-.
BibTeX @misc{4ortxyz_pc-p-16-0-18-1-11z-_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{PC(P-16:0/18:1(11Z))}}, year = {2026}, url = {https://4ort.xyz/entity/pc-p-16-0-18-1-11z-}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): PC(P-16:0/18:1(11Z)) — https://4ort.xyz/entity/pc-p-16-0-18-1-11z- (retrieved 2026-05-03)

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