# (R)-6-hydroxymellein

> chemical compound

**Wikidata**: [Q4641539](https://www.wikidata.org/wiki/Q4641539)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/6-Hydroxymellein)  
**Source**: https://4ort.xyz/entity/r-6-hydroxymellein


## References

1. [CAS Common Chemistry](https://commonchemistry.cas.org/detail?cas_rn=70901-60-9)
2. 3,4-Dihydro-6,8-dihydroxy-3-methyl-1H-2-benzopyran-1-one. PubChem
3. ChEBI release 2020-09-01
4. Gene Ontology release 2020-05-02
5. 6-Hydroxymellein. ChemSpider
6. ChEBI release 2019-10-02
7. Metabolites with nematicidal and antimicrobial activities from the ascomycete Lachnum papyraceum (Karst.) Karst. III. Production of novel isocoumarin derivatives, isolation, and biological activities.
8. Metabolites with Nematicidal and Antimicrobial Activities from the Ascomycete Lachnum papyraceum(Karst.) Karst. V. Production, Isolation and Biological Activities of Bromine-containing Mycorrhizin and Lachnumon Derivatives and Four Additional New Bio
9. New Metabolites with Nematicidal and Antimicrobial Activities from the Ascomycete Lachnum papyraceum(Karst.) Karsts. VI. Structure Determination of Non-halogenated Metabolites Structurally Related to Mycorrhizin A
10. Cassiadinine, a chromone alkaloid and (+)-6-hydroxy-mellein, a dihydroisocoumarin from Cassia siamea
11. Toxins Produced by the Dogwood Anthracnose Fungus Discula sp.
12. Phytotoxins produced byTubakia dryina
13. Aspterric acid and 6-hydroxymellein, inhibitors of pollen development in Arabidopsis thaliana, produced by Aspergillus terreus
14. Three New Compounds from Aspergillus terreus PT06-2 Grown in a High Salt Medium
15. Metabolomics-guided analysis of isocoumarin production by Streptomyces species MBT76 and biotransformation of flavonoids and phenylpropanoids
16. Biological activities of extracts from endophytic fungi isolated from Garcinia plants
17. Myxostiolide, Myxostiol, and Clavatoic Acid, Plant Growth Regulators from the FungusMyxotrichumstipitatum
18. Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique
19. UniChem