BioViotica

5-Methylmellein

Name: 5-Methylmellein
Brand: BioViotica
SKU: BVT-0413
Price: 85.00 CHF
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BVT-0413-M0011 mgCHF 85.00

Specifications / Handling

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Product Details
Synonyms	5- Methylochracin; 3,4-Dihydro-8-hydroxy-3,5-dimethyl-1H-2-benzopyran1- one; 3,4-Dihydro-8-hydroxy-3,5-dimethylisocoumarin
Product Type	Chemical
Properties
Formula	C₁₁H₁₂O₃
MW	192.2
CAS	7734-92-1
Source/Host Chemicals	Isolated from Fusicoccum amygdalis.
Purity Chemicals	≥98% (HPLC)
Appearance	Pale yellow powder.
Solubility	Soluble in DMSO, chloroform or dichloromethane.
Identity	Determined by ¹H-NMR.
Declaration	Manufactured by BioViotica.
InChi Key	YETSBBYQOFXYGV-SSDOTTSWSA-N
Smiles	C[C@@H]1CC2=C(C(O)=CC=C2C)C(=O)O1
Shipping and Handling
Shipping	AMBIENT
Short Term Storage	+4°C
Long Term Storage	-20°C
Handling Advice	Protect from light when in solution.
Use/Stability	Stable for at least 1 year after receipt when stored at -20°C. After reconstitution protect from light at -20°C.
Documents
Safety Data Sheet	Download PDF
Product Specification Sheet
Datasheet	Download PDF

Product Description

Product-specific References

5-Methylmellein, a new natural dihydroisocoumarin: A. Ballio, et al.; Tetrahedron Lett. 1966, 3723 (1966)
(-)-5-Methylmellein and catechol derivatives from four semecarpus species: R.C. Carpenter, et al.; Phytochemistry 19, 445 (1980)
3-Methyl-3,4-dihydroisocoumarins and related compounds from the ascomycete family xylariaceae: J.R. Anderson & R.L. Edwards; J. Chem. Soc. Perkin Trans I 1983, 2185 (1983)
Dihydroisocoumarins from fungi: isolation, structure elucidation, circular dichroism and biological activity: K. Krohn, et al.; Phytochemistry 45, 313 (1997)
Nodulisporol and nodulisporone, novel specific inhibitors of human DNA polymerase λ from a fungus, Nodulisporium sp.: S. Kamisuki, et al.; Bioorg. Med. Chem. 15, 3109 (2007)
Bioactive aromatic derivatives from endophytic fungus, Cytospora sp.: S. Lu, et al.; Nat. Prod. Commun. 6, 661 (2011)
Guaiane sesquiterpenes from Biscogniauxia nummularia featuring potent antigerminative activity: S. Amand, et al.; J. Nat. Prod. 75, 798 (2012)

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