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linaclotide

chemical compound
ChemicalSubstance type_of_chemical_entity Q3832559
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linaclotide

Summary

linaclotide is a type of chemical entity[1]. linaclotide ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (148 views/month).[2]

Key Facts

  • linaclotide's instance of is recorded as type of chemical entity[3].
  • linaclotide's chemical structure is recorded as Linaclotide structure.svg[4].
  • linaclotide's physically interacts with is recorded as Guanylate cyclase 2C[5].
  • linaclotide's CAS Registry Number is recorded as 851199-59-2[6].
  • linaclotide's EC number is recorded as 812-291-9[7].
  • linaclotide's canonical SMILES is recorded as CC1C(=O)NC2CSSCC3C(=O)NC(C(=O)NC(C(=O)NC(CSSCC(NC(=O)CNC(=O)C(NC2=O)C(C)O)C(=O)NC(CC4=CC=C(C=C4)O)C(=O)O)C(=O)NC(CSSCC(C(=O)N3)N)C(=O)NC(C(=O)N5CCCC5C(=O)N1)CC(=O)N)CC6=CC=C(C=C6)O)CCC(=O)O[8].
  • linaclotide's InChI is recorded as InChI=1S/C59H79N15O21S6/c1-26-47(82)69-41-25-101-99-22-38-52(87)65-33(13-14-45(80)81)49(84)66-34(16-28-5-9-30(76)10-6-28)50(85)71-40(54(89)72-39(23-97-96-20-32(60)48(83)70-38)53(88)67-35(18-43(61)78)58(93)74-15-3-4-42(74)56(91)63-26)24-100-98-21-37(64-44(79)19-62-57(92)46(27(2)75)73-55(41)90)51(86)68-36(59(94)95)17-29-7-11-31(77)12-8-29/h5-12,26-27,32-42,46,75-77H,3-4,13-25,60H2,1-2H3,(H2,61,78)(H,62,92)(H,63,91)(H,64,79)(H,65,87)(H,66,84)(H,67,88)(H,68,86)(H,69,82)(H,70,83)(H,71,85)(H,72,89)(H,73,90)(H,80,81)(H,94,95)/t26-,27+,32-,33-,34-,35-,36-,37-,38-,39-,40-,41-,42-,46-/m0/s1[9].
  • linaclotide's InChIKey is recorded as KXGCNMMJRFDFNR-WDRJZQOASA-N[10].
  • linaclotide's ATC code is recorded as A06AX04[11].
  • linaclotide's chemical formula is recorded as C₅₉H₇₉N₁₅O₂₁S₆[12].
  • linaclotide's subclass of is recorded as biogenic cyclopeptide[13].
  • linaclotide's has use is recorded as medication[14].
  • linaclotide's Commons category is recorded as Linaclotide[15].
  • linaclotide's MeSH descriptor ID is recorded as C523483[16].
  • linaclotide's ChEMBL ID is recorded as CHEMBL3301675[17].
  • linaclotide's Guide to Pharmacology Ligand ID is recorded as 5017[18].
  • linaclotide's Freebase ID is recorded as /m/0dd8vmm[19].
  • linaclotide's ChemSpider ID is recorded as 17314504[20].
  • linaclotide's PubChem CID is recorded as 16158208[21].
  • linaclotide's KEGG ID is recorded as D09355[22].
  • linaclotide's ChEBI ID is recorded as 68551[23].
  • linaclotide's found in taxon is recorded as Escherichia coli[24].
  • linaclotide's DrugBank ID is recorded as DB08890[25].
  • linaclotide's isomeric SMILES is recorded as C[C@H]1C(=O)N[C@H]2CSSC[C@H]3C(=O)NC@HCCC(=O)OC@@HC(=O)N[C@@H]">[26].
  • linaclotide's HSDB ID is recorded as 8224[27].

Why It Matters

linaclotide ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (148 views/month).[2] linaclotide has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] linaclotide is known by 5 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . DrugBank. wikidata.org.
  10. [12] ↑ . PubChem. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . DrugBank. wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  15. [17] ↑ . ChEMBL. Retrieved . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . Q2311683. Retrieved . wikidata.org.
  19. [21] ↑ . PubChem. Retrieved . wikidata.org.
  20. [22] ↑ . ChEBI. Retrieved . wikidata.org.
  21. [23] ↑ . ChEMBL. Retrieved . wikidata.org.
  22. [24] ↑ . Rectification of two Escherichia coli heat-stable enterotoxin allele sequences and lack of biological effect of changing the carboxy-terminal tyrosine to histidine. wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . PubChem. Retrieved . wikidata.org.
  25. [27] ↑ . Hazardous Substances Data Bank. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . Wikidata aliases. 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). linaclotide. Retrieved May 3, 2026, from https://4ort.xyz/entity/linaclotide
MLA “linaclotide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/linaclotide.
BibTeX @misc{4ortxyz_linaclotide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{linaclotide}}, year = {2026}, url = {https://4ort.xyz/entity/linaclotide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): linaclotide — https://4ort.xyz/entity/linaclotide (retrieved 2026-05-03)

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