N(1)-methyl-cGMP

chemical compound
ChemicalSubstance group_of_stereoisomers Q27157947
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N(1)-methyl-cGMP

Summary

N(1)-methyl-cGMP is a group of stereoisomers[1].

Key Facts

  • N(1)-methyl-cGMP's instance of is recorded as group of stereoisomers[2].
  • N(1)-methyl-cGMP's CAS Registry Number is recorded as 78033-41-7[3].
  • N(1)-methyl-cGMP's canonical SMILES is recorded as CN1C(=O)C2=C(N=C1N)N(C=N2)C3C(C4C(O3)COP(=O)(O4)O)O[4].
  • N(1)-methyl-cGMP's InChI is recorded as InChI=1S/C11H14N5O7P/c1-15-9(18)5-8(14-11(15)12)16(3-13-5)10-6(17)7-4(22-10)2-21-24(19,20)23-7/h3-4,6-7,10,17H,2H2,1H3,(H2,12,14)(H,19,20)/t4-,6-,7-,10-/m1/s1[5].
  • N(1)-methyl-cGMP's InChIKey is recorded as FBEZEINIPFPIME-KQYNXXCUSA-N[6].
  • N(1)-methyl-cGMP's chemical formula is recorded as C₁₁H₁₄N₅O₇P[7].
  • N(1)-methyl-cGMP's subclass of is recorded as purine nucleotides[8].
  • N(1)-methyl-cGMP's ChemSpider ID is recorded as 34999513[9].
  • N(1)-methyl-cGMP's PubChem CID is recorded as 44755113[10].
  • N(1)-methyl-cGMP's ChEBI ID is recorded as 84632[11].
  • N(1)-methyl-cGMP's found in taxon is recorded as Pelargonium sidoides[12].
  • N(1)-methyl-cGMP's Reaxys registry number is recorded as 8581728[13].
  • N(1)-methyl-cGMP's isomeric SMILES is recorded as CN1C(=O)C2=C(N=C1N)N(C=N2)[C@H]3C@@HOC@@HO">[14].
  • N(1)-methyl-cGMP's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+359.063084'}[15].
  • N(1)-methyl-cGMP's SureChEMBL ID is recorded as 23920881[16].
  • N(1)-methyl-cGMP's DSSTox substance ID is recorded as DTXSID001204033[17].
  • N(1)-methyl-cGMP's UniChem compound ID is recorded as 60688106[18].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . 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] . Benzopyranones and their sulfate esters from Pelargonium sidoides. wikidata.org.
  12. [13] . ChEBI. Retrieved . wikidata.org.
  13. [14] . PubChem. Retrieved . wikidata.org.
  14. [15] . PubChem. Retrieved . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . 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(1)-methyl-cGMP. Retrieved May 3, 2026, from https://4ort.xyz/entity/n-1-methyl-cgmp
MLA “N(1)-methyl-cGMP.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/n-1-methyl-cgmp.
BibTeX @misc{4ortxyz_n-1-methyl-cgmp_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{N(1)-methyl-cGMP}}, year = {2026}, url = {https://4ort.xyz/entity/n-1-methyl-cgmp}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): N(1)-methyl-cGMP — https://4ort.xyz/entity/n-1-methyl-cgmp (retrieved 2026-05-03)

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