Haematopodin

group of stereoisomers with the chemical formula C₁₃H₁₂N₂O₃
ChemicalSubstance group_of_stereoisomers Q104167479
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Haematopodin

Summary

Haematopodin is a group of stereoisomers[1].

Key Facts

  • Haematopodin's instance of is recorded as group of stereoisomers[2].
  • Haematopodin's canonical SMILES is recorded as O=C1C=C2C3=C(NC=C3CC4OCCCN24)C1=O[3].
  • Haematopodin's InChI is recorded as InChI=1S/C13H12N2O3/c16-9-5-8-11-7(6-14-12(11)13(9)17)4-10-15(8)2-1-3-18-10/h5-6,10,14H,1-4H2[4].
  • Haematopodin's InChIKey is recorded as GTVMGUBGOSWMOJ-UHFFFAOYSA-N[5].
  • Haematopodin's chemical formula is recorded as C₁₃H₁₂N₂O₃[6].
  • Haematopodin's subclass of is recorded as pyrrolo[4,3,2-de]quinoline alkaloid[7].
  • Haematopodin's PubChem CID is recorded as 10857709[8].
  • Haematopodin's ChEBI ID is recorded as 174261[9].
  • Haematopodin's Human Metabolome Database ID is recorded as HMDB0040734[10].
  • Haematopodin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+244.084792244'}[11].
  • Haematopodin's SureChEMBL ID is recorded as 31734829[12].
  • Haematopodin's UniChem compound ID is recorded as 32009549[13].

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APA 4ort.xyz Knowledge Graph. (2026). Haematopodin. Retrieved May 3, 2026, from https://4ort.xyz/entity/haematopodin-q104167479
MLA “Haematopodin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/haematopodin-q104167479.
BibTeX @misc{4ortxyz_haematopodin-q104167479_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Haematopodin}}, year = {2026}, url = {https://4ort.xyz/entity/haematopodin-q104167479}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Haematopodin — https://4ort.xyz/entity/haematopodin-q104167479 (retrieved 2026-05-03)

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