rocaglamide

chemical compound
ChemicalSubstance type_of_chemical_entity Q3437403
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rocaglamide

Summary

rocaglamide is a type of chemical entity[1]. rocaglamide ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (13 views/month).[2]

Key Facts

  • rocaglamide's instance of is recorded as type of chemical entity[3].
  • rocaglamide's CAS Registry Number is recorded as 84573-16-0[4].
  • rocaglamide's canonical SMILES is recorded as CN(C)C(=O)C1C(C2(C(C1O)(C3=C(C=C(C=C3O2)OC)OC)O)C4=CC=C(C=C4)OC)C5=CC=CC=C5[5].
  • rocaglamide's InChI is recorded as InChI=1S/C29H31NO7/c1-30(2)27(32)23-24(17-9-7-6-8-10-17)29(18-11-13-19(34-3)14-12-18)28(33,26(23)31)25-21(36-5)15-20(35-4)16-22(25)37-29/h6-16,23-24,26,31,33H,1-5H3/t23-,24-,26-,28+,29+/m1/s1[6].
  • rocaglamide's InChIKey is recorded as DAPAQENNNINUPW-IDAMAFBJSA-N[7].
  • rocaglamide's chemical formula is recorded as C₂₉H₃₁NO₇[8].
  • rocaglamide's subclass of is recorded as flavagline[9].
  • rocaglamide's ChEMBL ID is recorded as CHEMBL438139[10].
  • rocaglamide's Freebase ID is recorded as /m/0h_crdw[11].
  • rocaglamide's UNII is recorded as FRG4N852F7[12].
  • rocaglamide's ChemSpider ID is recorded as 293974[13].
  • rocaglamide's PubChem CID is recorded as 331783[14].
  • rocaglamide's ChEBI ID is recorded as 66309[15].
  • rocaglamide's found in taxon is recorded as Aglaia odorata[16].
  • rocaglamide's found in taxon is recorded as Aglaia roxburghiana[17].
  • rocaglamide's found in taxon is recorded as Aglaia basiphylla[18].
  • rocaglamide's found in taxon is recorded as Aglaia elliptifolia[19].
  • rocaglamide's found in taxon is recorded as Aglaia rimosa[20].
  • rocaglamide's found in taxon is recorded as Aglaia elliptica[21].
  • rocaglamide's found in taxon is recorded as Aglaia elaeagnoidea[22].
  • rocaglamide's found in taxon is recorded as Aglaia formosana[23].
  • rocaglamide's DrugBank ID is recorded as DB15495[24].
  • rocaglamide's Reaxys registry number is recorded as 4219080[25].
  • rocaglamide's isomeric SMILES is recorded as CN(C)C(=O)[C@@H]1C@HC5=CC=CC=C5C@HC5=CC=CC=C5">[26].
  • rocaglamide's mass is recorded as {'unit': 'Q483261', 'amount': '+505.21'}[27].

Why It Matters

rocaglamide ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (13 views/month).[2] rocaglamide is known by 4 alternative names across languages and contexts.[28]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . ChEMBL. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Q2311683. Retrieved . wikidata.org.
  12. [14] . PubChem. Retrieved . wikidata.org.
  13. [15] . ChEBI. Retrieved . wikidata.org.
  14. [16] . Insecticidal 1H-cyclopentatetrahydro[b]benzofurans from Aglaia odorata. wikidata.org.
  15. [17] . Insecticidal natural products: new rocaglamide derivatives fromAglaia roxburghiana. wikidata.org.
  16. [18] . Insecticidal flavaglines and other compounds from Fijian Aglaia species. wikidata.org.
  17. [19] . Cytotoxic and antiplatelet aggregation principles from Aglaia elliptifolia. wikidata.org.
  18. [20] . Cytotoxic and antiplatelet aggregation principles from Aglaia elliptifolia. wikidata.org.
  19. [21] . Insecticidal rocaglamide derivatives from Aglaia elliptica and A. harmsiana. wikidata.org.
  20. [22] . Cytotoxic cyclopenta[b]benzofuran derivatives from the stem bark of Aglaia formosana. wikidata.org.
  21. [23] . Cytotoxic cyclopenta[b]benzofuran derivatives from the stem bark of Aglaia formosana. wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . ChEBI. Retrieved . wikidata.org.
  24. [26] . PubChem. Retrieved . wikidata.org.
  25. [27] . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata aliases. wikidata.org.

📑 Cite this page

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). rocaglamide. Retrieved May 3, 2026, from https://4ort.xyz/entity/rocaglamide
MLA “rocaglamide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rocaglamide.
BibTeX @misc{4ortxyz_rocaglamide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{rocaglamide}}, year = {2026}, url = {https://4ort.xyz/entity/rocaglamide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): rocaglamide — https://4ort.xyz/entity/rocaglamide (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 4w ago · KaleemBot bot · 2026-04-30 view diff on Wikidata ↗
    Subclass of flavagline
    Found in taxon Aglaia odorata, Aglaia roxburghiana, Aglaia basiphylla +5
    Mass {'unit': 'Q483261', 'amount': '+505.21'}
    Stereoisomer of (1S,2S,3S,3aR,8bS)-1,8b-dihydroxy-6,8-dimethoxy-3a-(4-methoxyphenyl)-N,N-dimethyl-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxamide
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:روکا گلامائڈ]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.