N(6)-butyryl-cAMP

chemical compound
ChemicalSubstance group_of_stereoisomers Q27157909
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N(6)-butyryl-cAMP

Summary

N(6)-butyryl-cAMP is a group of stereoisomers[1].

Key Facts

  • N(6)-butyryl-cAMP's instance of is recorded as group of stereoisomers[2].
  • N(6)-butyryl-cAMP's CAS Registry Number is recorded as 13117-60-7[3].
  • N(6)-butyryl-cAMP's canonical SMILES is recorded as CCCC(=O)NC1=NC=NC2=C1N=CN2C3C(C4C(O3)COP(=O)(O4)O)O[4].
  • N(6)-butyryl-cAMP's InChI is recorded as InChI=1S/C14H18N5O7P/c1-2-3-8(20)18-12-9-13(16-5-15-12)19(6-17-9)14-10(21)11-7(25-14)4-24-27(22,23)26-11/h5-7,10-11,14,21H,2-4H2,1H3,(H,22,23)(H,15,16,18,20)/t7-,10-,11-,14-/m1/s1[5].
  • N(6)-butyryl-cAMP's InChIKey is recorded as NVGDLMUKSMHEQT-FRJWGUMJSA-N[6].
  • N(6)-butyryl-cAMP's chemical formula is recorded as C₁₄H₁₈N₅O₇P[7].
  • N(6)-butyryl-cAMP's subclass of is recorded as chemical compound[8].
  • N(6)-butyryl-cAMP's ChemSpider ID is recorded as 102951[9].
  • N(6)-butyryl-cAMP's PubChem CID is recorded as 115029[10].
  • N(6)-butyryl-cAMP's ChEBI ID is recorded as 84605[11].
  • N(6)-butyryl-cAMP's Reaxys registry number is recorded as 1054786[12].
  • N(6)-butyryl-cAMP's isomeric SMILES is recorded as CCCC(=O)NC1=NC=NC2=C1N=CN2[C@H]3C@@HOC@@HO">[13].
  • N(6)-butyryl-cAMP's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+399.094385'}[14].
  • N(6)-butyryl-cAMP's SureChEMBL ID is recorded as 30085324[15].
  • N(6)-butyryl-cAMP's SureChEMBL ID is recorded as 9635980[16].
  • N(6)-butyryl-cAMP's DSSTox substance ID is recorded as DTXSID60927103[17].
  • N(6)-butyryl-cAMP's DSSTOX compound identifier is recorded as DTXCID801355903[18].
  • N(6)-butyryl-cAMP's UniChem compound ID is recorded as 32037145[19].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . Q2311683. Retrieved . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . 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). N(6)-butyryl-cAMP. Retrieved May 3, 2026, from https://4ort.xyz/entity/n-6-butyryl-camp
MLA “N(6)-butyryl-cAMP.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/n-6-butyryl-camp.
BibTeX @misc{4ortxyz_n-6-butyryl-camp_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{N(6)-butyryl-cAMP}}, year = {2026}, url = {https://4ort.xyz/entity/n-6-butyryl-camp}, note = {Accessed: 2026-05-03}}
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