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mammea A/BB

group of stereoisomers with the chemical formula C₂₅H₂₆O₅
ChemicalSubstance group_of_stereoisomers Q105387011
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mammea A/BB

Summary

mammea A/BB is a group of stereoisomers[1].

Key Facts

  • mammea A/BB's instance of is recorded as group of stereoisomers[2].
  • mammea A/BB's CAS Registry Number is recorded as 6916-62-7[3].
  • mammea A/BB's canonical SMILES is recorded as O=C1OC=2C(=C(O)C(=C(O)C2C(=C1)C=3C=CC=CC3)CC=C(C)C)C(=O)C(C)CC[4].
  • mammea A/BB's InChI is recorded as InChI=1S/C25H26O5/c1-5-15(4)22(27)21-24(29)17(12-11-14(2)3)23(28)20-18(13-19(26)30-25(20)21)16-9-7-6-8-10-16/h6-11,13,15,28-29H,5,12H2,1-4H3[5].
  • mammea A/BB's InChIKey is recorded as ZZRRSYITGMMRPP-UHFFFAOYSA-N[6].
  • mammea A/BB's chemical formula is recorded as C₂₅H₂₆O₅[7].
  • mammea A/BB's subclass of is recorded as 4-phenylcoumarin flavonoid[8].
  • mammea A/BB's PubChem CID is recorded as 11750116[9].
  • mammea A/BB's ChEBI ID is recorded as 175252[10].
  • mammea A/BB's found in taxon is recorded as Mammea harmandii[11].
  • mammea A/BB's found in taxon is recorded as Marila podantha[12].
  • mammea A/BB's found in taxon is recorded as Mesua ferrea[13].
  • mammea A/BB's found in taxon is recorded as Mammea americana[14].
  • mammea A/BB's Human Metabolome Database ID is recorded as HMDB0030780[15].
  • mammea A/BB's LIPID MAPS ID is recorded as LMPK12100021[16].
  • mammea A/BB's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+406.178023932'}[17].
  • mammea A/BB's SureChEMBL ID is recorded as 31237267[18].
  • mammea A/BB's SureChEMBL ID is recorded as 6907224[19].
  • mammea A/BB's DSSTox substance ID is recorded as DTXSID101318164[20].
  • mammea A/BB's UniChem compound ID is recorded as 349852[21].

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] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . ChEBI release 2022-06-13. wikidata.org.
  10. [11] ↑ . Natural and Semisynthetic Mammea-Type Isoprenylated Dihydroxycoumarins Uncouple Cellular Respiration. wikidata.org.
  11. [12] ↑ . Cytotoxic 4-phenylcoumarins from the leaves of Marila pluricostata.. wikidata.org.
  12. [13] ↑ . 6-Acylcoumarins from Mesua racemosa. wikidata.org.
  13. [14] ↑ . Extractives of Mammea americana L. Part II. The 4-phenylcoumarins. Isolation and structure of Mammea A/AA, A/A cyclo D, A/BA, A/AB, and A/BB. wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . 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). mammea A/BB. Retrieved May 3, 2026, from https://4ort.xyz/entity/mammea-a-bb
MLA “mammea A/BB.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/mammea-a-bb.
BibTeX @misc{4ortxyz_mammea-a-bb_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{mammea A/BB}}, year = {2026}, url = {https://4ort.xyz/entity/mammea-a-bb}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): mammea A/BB — https://4ort.xyz/entity/mammea-a-bb (retrieved 2026-05-03)

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