palmitoyl-CoA(4-)

chemical compound

ChemicalSubstance group_of_stereoisomers Q27124538

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palmitoyl-CoA(4-)

Summary

palmitoyl-CoA(4-) is a group of stereoisomers^[1].

Key Facts

palmitoyl-CoA(4-)'s instance of is recorded as group of stereoisomers^[2].
palmitoyl-CoA(4-)'s canonical SMILES is recorded as CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)([O-])OP(=O)([O-])OCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)([O-])[O-])O^[3].
palmitoyl-CoA(4-)'s chemical formula is recorded as C₃₇H₆₂N₇O₁₇P₃S⁴⁻^[4].
palmitoyl-CoA(4-) is a type of chemical compound^[5].
palmitoyl-CoA(4-) is part of carnitine O-palmitoyltransferase activity^[6].
palmitoyl-CoA(4-) is part of ecdysone O-acyltransferase activity^[7].
palmitoyl-CoA(4-) is part of serine C-palmitoyltransferase activity^[8].
palmitoyl-CoA(4-) is part of palmitoyl-CoA hydrolase activity^[9].
palmitoyl-CoA(4-) is part of protein-cysteine S-palmitoyltransferase activity^[10].
palmitoyl-CoA(4-) is part of hexadecanal dehydrogenase (acylating) activity^[11].
palmitoyl-CoA(4-) is part of dolichol O-acyltransferase activity^[12].
palmitoyl-CoA(4-) is part of CoA-dependent peptidyl-lysine N6-palmitoyltransferase activity^[13].
palmitoyl-CoA(4-)'s isomeric SMILES is recorded as CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)C@@HO^C@@HO">[14].
palmitoyl-CoA(4-)'s mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+1001.31576873364'}^[15].
palmitoyl-CoA(4-)'s subject has role is recorded as primary metabolite^[16].

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Quick Facts

Instance of group of stereoisomers

Subclass of chemical compound

Part of carnitine O-palmitoyltransferase activity, ecdysone O-acyltransferase activity, serine C-palmitoyltransferase activity, palmitoyl-CoA hydrolase activity, protein-cysteine S-palmitoyltransferase activity, hexadecanal dehydrogenase (acylating) activity, dolichol O-acyltransferase activity, CoA-dependent peptidyl-lysine N6-palmitoyltransferase activity

Properties

Canonical smiles CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)([O-])OP(=O)([O-])OCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)([O-])[O-])O

Chemical formula C₃₇H₆₂N₇O₁₇P₃S⁴⁻

Isomeric smiles CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)([O-])OP(=O)([O-])OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)([O-])[O-])O

Mass +1001.31576873364

Subject has role primary metabolite

External References (7)

Chebi id 57379

Chemspider id 26330752

Inchi InChI=1S/C37H66N7O17P3S/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-28(46)65-21-20-39-27(45)18-19-40-35(49)32(48)37(2,3)23-58-64(55,56)61-63(53,54)57-22-26-31(60-62(50,51)52)30(47)36(59-26)44-25-43-29-33(38)41-24-42-34(29)44/h24-26,30-32,36,47-48H,4-23H2,1-3H3,(H,39,45)(H,40,49)(H,53,54)(H,55,56)(H2,38,41,42)(H2,50,51,52)/p-4/t26-,30-,31-,32+,36-/m1/s1

Inchikey MNBKLUUYKPBKDU-BBECNAHFSA-J

Pubchem cid 45266605

Swisslipids id SLM:000000383

Unichem compound id 1096228

🏷️ Also known as

en palmitoyl-CoA(4-)

References

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

Direct Wikidata claims

[2] ↑ palmitoyl-CoA(4-) — instance of (P31): group of stereoisomers. wikidata.org.
[3] ↑ palmitoyl-CoA(4-) — canonical SMILES (P233): CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)([O-])OP(=O)([O-])OCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)([O-])[O-])O. PubChem. Retrieved 2016-10-06. wikidata.org.
[4] ↑ palmitoyl-CoA(4-) — chemical formula (P274): C₃₇H₆₂N₇O₁₇P₃S⁴⁻. wikidata.org.
[5] ↑ palmitoyl-CoA(4-) — subclass of (P279): chemical compound. wikidata.org.
[6] ↑ palmitoyl-CoA(4-) — part of (P361): carnitine O-palmitoyltransferase activity. Gene Ontology release 2020-05-02. wikidata.org.
[7] ↑ palmitoyl-CoA(4-) — part of (P361): ecdysone O-acyltransferase activity. Gene Ontology release 2020-05-02. wikidata.org.
[8] ↑ palmitoyl-CoA(4-) — part of (P361): serine C-palmitoyltransferase activity. Gene Ontology release 2020-05-02. wikidata.org.
[9] ↑ palmitoyl-CoA(4-) — part of (P361): palmitoyl-CoA hydrolase activity. Gene Ontology release 2020-05-02. wikidata.org.
[10] ↑ palmitoyl-CoA(4-) — part of (P361): protein-cysteine S-palmitoyltransferase activity. Gene Ontology release 2020-05-02. wikidata.org.
[11] ↑ palmitoyl-CoA(4-) — part of (P361): hexadecanal dehydrogenase (acylating) activity. Gene Ontology release 2020-05-02. wikidata.org.
[12] ↑ palmitoyl-CoA(4-) — part of (P361): dolichol O-acyltransferase activity. geneontology.org. Retrieved 2021-02-01. geneontology.org. Provenance: wikidata.org.
[13] ↑ palmitoyl-CoA(4-) — part of (P361): CoA-dependent peptidyl-lysine N6-palmitoyltransferase activity. geneontology.org. Retrieved 2022-05-25. geneontology.org. Provenance: wikidata.org.
[14] ↑ palmitoyl-CoA(4-) — isomeric SMILES (P2017): CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)([O-])OP(=O)([O-])OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)([O-])[O-])O. PubChem. Retrieved 2016-10-06. wikidata.org.
[15] ↑ palmitoyl-CoA(4-) — mass (P2067): {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+1001.31576873364'}. wikidata.org.
[16] ↑ palmitoyl-CoA(4-) — subject has role (P2868): primary metabolite. Reactome. reactome.org. Provenance: wikidata.org.

Class ancestry

[1] ↑ palmitoyl-CoA(4-) is an instance of group of stereoisomers (Q59199015) [P31, primary]. 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). palmitoyl-CoA(4-). Retrieved May 3, 2026, from https://4ort.xyz/entity/palmitoyl-coa-4-

MLA “palmitoyl-CoA(4-).” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/palmitoyl-coa-4-.

BibTeX

@misc{4ortxyz_palmitoyl-coa-4-_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{palmitoyl-CoA(4-)}}, year = {2026}, url = {https://4ort.xyz/entity/palmitoyl-coa-4-}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): palmitoyl-CoA(4-) — https://4ort.xyz/entity/palmitoyl-coa-4- (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/palmitoyl-coa-4- · Last refreshed: May 3, 2026

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

13w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗

Isomeric smiles → CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)([

Subclass of → chemical compound

Subject has role → primary metabolite

Unichem compound id → 1096228

+ 13 other properties edited (see Wikidata diff for full list)

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