Retrocalamin

group of stereoisomers with the chemical formula C₂₄H₃₀O₉
ChemicalSubstance group_of_stereoisomers Q111734415
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Retrocalamin

Summary

Retrocalamin is a group of stereoisomers[1].

Key Facts

  • Retrocalamin's instance of is recorded as group of stereoisomers[2].
  • Retrocalamin's canonical SMILES is recorded as O=C(OC)CC(O)C1(C)CC(=O)C(O)C2(C)C1CCC3(C)C(OC(=O)C4OC432)C5=COC=C5[3].
  • Retrocalamin's InChI is recorded as InChI=1S/C24H30O9/c1-21(15(26)9-16(27)30-4)10-13(25)17(28)23(3)14(21)5-7-22(2)18(12-6-8-31-11-12)32-20(29)19-24(22,23)33-19/h6,8,11,14-15,17-19,26,28H,5,7,9-10H2,1-4H3/t14-,15?,17?,18+,19-,21+,22+,23+,24-/m1/s1[4].
  • Retrocalamin's InChIKey is recorded as HMNKPIJMXBZMJF-ZLOQDTKLSA-N[5].
  • Retrocalamin's chemical formula is recorded as C₂₄H₃₀O₉[6].
  • Retrocalamin's subclass of is recorded as chemical compound[7].
  • Retrocalamin's PubChem CID is recorded as 101593104[8].
  • Retrocalamin's ChEBI ID is recorded as 190031[9].
  • Retrocalamin's found in taxon is recorded as Skimmia japonica[10].
  • Retrocalamin's found in taxon is recorded as Citrus reticulata[11].
  • Retrocalamin's found in taxon is recorded as Citrus × deliciosa[12].
  • Retrocalamin's isomeric SMILES is recorded as COC(=O)CC(O)[C@@]1(C)CC(=O)C(O)[C@]2(C)[C@@H]1CC[C@@]1(C)C@HOC(=O)[C@H]3O[C@]312C@HOC(=O)[C@H]3O[C@]312">[13].
  • Retrocalamin's KNApSAcK ID is recorded as C00057536[14].
  • Retrocalamin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+462.18898254'}[15].
  • Retrocalamin's SureChEMBL ID is recorded as 29934431[16].
  • Retrocalamin's DSSTox substance ID is recorded as DTXSID301317879[17].
  • Retrocalamin's UniChem compound ID is recorded as 96668657[18].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . PubChem. Retrieved . wikidata.org.
  8. [9] . ChEBI release 2022-06-13. wikidata.org.
  9. [10] . Limonoids in Miyamashikimi (Skimmia japonica Thunb.).. wikidata.org.
  10. [11] . Limonoids in citrus seeds: origin and relative concentration. wikidata.org.
  11. [12] . Limonoids in citrus seeds: origin and relative concentration. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . 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). Retrocalamin. Retrieved May 3, 2026, from https://4ort.xyz/entity/retrocalamin
MLA “Retrocalamin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/retrocalamin.
BibTeX @misc{4ortxyz_retrocalamin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Retrocalamin}}, year = {2026}, url = {https://4ort.xyz/entity/retrocalamin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Retrocalamin — https://4ort.xyz/entity/retrocalamin (retrieved 2026-05-03)

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