AdipoGen Life Sciences

Globosuxanthone A

CHF 90.00
In stock
AG-CN2-0174-C250250 µgCHF 90.00
AG-CN2-0174-M0011 mgCHF 270.00
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Product Details
Synonyms (1R,2R)-1,2,8-Trihydroxy-9-oxo-2,9-dihydro-1H-xanthene-1-carboxylate
Product Type Chemical
Properties
Formula

C15H12O7

MW 304.3
CAS 917091-74-8
Source/Host Chemicals Isolated from fungus (species unknown).
Purity Chemicals ≥95% (HPLC)
Appearance Yellow solid.
Solubility Soluble in ethanol, methanol or DMSO (all 1mg/ml).
InChi Key HEFOWMGZUBJFBY-BMIGLBTASA-N
Smiles OC1=C2C(OC(C=C[C@@H](O)[C@]3(C(OC)=O)O)=C3C2=O)=CC=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Keep cool and dry.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description
  • Potent anticancer agent. Inhibits cell growth, proliferation and survival of human tumor cells lines in vivo and in vitro.
  • Exhibits strong cytotoxicity against a panel of human solid tumor cell lines, disrupting the cell cycle leading to the accumulation of cells in either G2/M or S phase and inducing classic signs of apoptosis.
  • Antifungal agent against Candida albicans.
Product References
  1. A new dihydroxanthenone from a plant-associated strain of the fungus Chaetomium globosum demonstrates anticancer activity: E.M.K.Wijeratne, et al.; Bioorg. Med. Chem. 14, 7917 (2006)
  2. Absolute Configurations of Globosuxanthone A and Secondary Metabolites from Microdiplodia sp.- A Novel Solid-State CD/TDDFT Approach: H. Hussain, et al.; Eur. J. Org. Chem. 2007, 292 (2007)
  3. A new dibenz[b,e]oxepine derivative, 1-hydroxy-10-methoxy-dibenz[b,e]oxepin-6,11-dione, from a marine-derived fungus, Beauveria bassiana TPU942; H. Yamazaki, et al.; Mar. Drugs 10, 2691 (2012)
  4. Dihydroxanthenones from the fermentation product of an endophytic fungus Gliomastix murorum: H.Y. Yang, et al.; J. Asian Nat. Prod. Res. 17, 319 (2015)
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