(R)-6-hydroxymellein

chemical compound
ChemicalSubstance type_of_chemical_entity Q4641539
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(R)-6-hydroxymellein

Summary

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

Key Facts

  • (R)-6-hydroxymellein's instance of is recorded as type of chemical entity[3].
  • (R)-6-hydroxymellein's CAS Registry Number is recorded as 70901-60-9[4].
  • (R)-6-hydroxymellein's canonical SMILES is recorded as CC1CC2=CC(=CC(=C2C(=O)O1)O)O[5].
  • (R)-6-hydroxymellein's InChI is recorded as InChI=1S/C10H10O4/c1-5-2-6-3-7(11)4-8(12)9(6)10(13)14-5/h3-5,11-12H,2H2,1H3/t5-/m1/s1[6].
  • (R)-6-hydroxymellein's InChIKey is recorded as DHLPMLVSBRRUGA-RXMQYKEDSA-N[7].
  • (R)-6-hydroxymellein's chemical formula is recorded as C₁₀H₁₀O₄[8].
  • (R)-6-hydroxymellein's subclass of is recorded as 6-Hydroxymellein[9].
  • (R)-6-hydroxymellein's part of is recorded as 6-hydroxymellein O-methyltransferase activity[10].
  • (R)-6-hydroxymellein's Freebase ID is recorded as /m/0jzsywg[11].
  • (R)-6-hydroxymellein's UNII is recorded as PUH8Z0Q805[12].
  • (R)-6-hydroxymellein's ChemSpider ID is recorded as 388784[13].
  • (R)-6-hydroxymellein's PubChem CID is recorded as 172675[14].
  • (R)-6-hydroxymellein's KEGG ID is recorded as C02379[15].
  • (R)-6-hydroxymellein's ChEBI ID is recorded as 16368[16].
  • (R)-6-hydroxymellein's found in taxon is recorded as Lachnum papyraceum[17].
  • (R)-6-hydroxymellein's found in taxon is recorded as Senna siamea[18].
  • (R)-6-hydroxymellein's found in taxon is recorded as Discula[19].
  • (R)-6-hydroxymellein's found in taxon is recorded as Dicarpella dryina[20].
  • (R)-6-hydroxymellein's found in taxon is recorded as Tubakia dryina[21].
  • (R)-6-hydroxymellein's found in taxon is recorded as Aspergillus terreus[22].
  • (R)-6-hydroxymellein's found in taxon is recorded as Streptomyces[23].
  • (R)-6-hydroxymellein's found in taxon is recorded as Garcinia atroviridis[24].
  • (R)-6-hydroxymellein's found in taxon is recorded as Myxotrichum stipitatum[25].
  • (R)-6-hydroxymellein's found in taxon is recorded as Handroanthus impetiginosum[26].
  • (R)-6-hydroxymellein's found in taxon is recorded as Handroanthus impetiginosus[27].

Why It Matters

(R)-6-hydroxymellein ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (2 views/month).[2]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . ChEBI release 2020-09-01. wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Gene Ontology release 2020-05-02. wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Q2311683. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . ChEBI release 2019-10-02. wikidata.org.
  15. [17] . Metabolites with nematicidal and antimicrobial activities from the ascomycete Lachnum papyraceum (Karst.) Karst. III. Production of novel isocoumarin derivatives, isolation, and biological activities.. wikidata.org.
  16. [18] . Cassiadinine, a chromone alkaloid and (+)-6-hydroxy-mellein, a dihydroisocoumarin from Cassia siamea. wikidata.org.
  17. [19] . Toxins Produced by the Dogwood Anthracnose Fungus Discula sp.. wikidata.org.
  18. [20] . Phytotoxins produced byTubakia dryina. wikidata.org.
  19. [21] . Phytotoxins produced byTubakia dryina. wikidata.org.
  20. [22] . Aspterric acid and 6-hydroxymellein, inhibitors of pollen development in Arabidopsis thaliana, produced by Aspergillus terreus. wikidata.org.
  21. [23] . Metabolomics-guided analysis of isocoumarin production by Streptomyces species MBT76 and biotransformation of flavonoids and phenylpropanoids. wikidata.org.
  22. [24] . Biological activities of extracts from endophytic fungi isolated from Garcinia plants. wikidata.org.
  23. [25] . Myxostiolide, Myxostiol, and Clavatoic Acid, Plant Growth Regulators from the FungusMyxotrichumstipitatum. wikidata.org.
  24. [26] . Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique. wikidata.org.
  25. [27] . Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). (R)-6-hydroxymellein. Retrieved May 3, 2026, from https://4ort.xyz/entity/r-6-hydroxymellein
MLA “(R)-6-hydroxymellein.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/r-6-hydroxymellein.
BibTeX @misc{4ortxyz_r-6-hydroxymellein_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(R)-6-hydroxymellein}}, year = {2026}, url = {https://4ort.xyz/entity/r-6-hydroxymellein}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (R)-6-hydroxymellein — https://4ort.xyz/entity/r-6-hydroxymellein (retrieved 2026-05-03)

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