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BioViotica
Rubrofusarin
130
CHF
CHF 130.00
In stock
BVT-0395-M0011 mgCHF 130.00
BVT-0395-M0055 mgCHF 395.00
| Product Details | |
|---|---|
| Synonyms | NSC 258316 |
| Product Type | Chemical |
| Properties | |
| Formula |
C15H12O5 |
| MW | 272.3 |
| CAS | 3567-00-8 |
| Source/Host Chemicals | Isolated from Fusarium graminearum. |
| Purity Chemicals | ≥98% (HPLC) |
| Appearance | Orange needles. |
| Solubility | Soluble in DMSO. Sparingly soluble in usual organic solvents. |
| Identity | Determined by 1H-NMR and UV. |
| Declaration | Manufactured by BioViotica. |
| InChi Key | FPNKCZKRICBAKG-UHFFFAOYSA-N |
| Smiles | COC1=CC2=C(C(O)=C1)C(O)=C1C(=O)C=C(C)OC1=C2 |
| 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 | |
| MSDS |
 Download PDF |
| Product Specification Sheet | |
| Datasheet |
Download PDF |
Description
- Monomer of aurofusarin.
- Mycotoxin.
- Anticancer and antimycobacterial compound in vivo.
- Moderate tyrosinase inhibitor.
- Anti-estrogenic.
Product References
- Structure of rubrofusarin: G.H. Stout, et al.; Chem. Indust. 1961, 289 (1961).
- Metabolic products of fungi. XXV. Synthesis of rubrofusarin and its derivatives: S. Shibata, et al.; Chem. Pharm. Bul.l (Tokyo) 15, 1757 (1967)
- The biosynthesis of rubrofusarin, a polyketide naphthopyrone from Fusarium culmorum: F.J. Leeper & J. Staunton; J. Chem. Soc. Perkin 1 1984, 2919 (1984).
- Biometic syntheses of the polyketide fungal metabolites alternariol and rubrofusarin: C. Abell, et al.; J. Chem. Soc. Chem. Comm. 1986, 15 (1986)
- Phenolic constituents of Cassia seeds and antibacterial effect of some naphthalenes and anthraquinones on methicillin-resistant St. aureus: T. Hatano, et al.; Chem. Pharm. Bull. 47, 1121 (1999)
- A new naphthopyrone derivative from Cassia quinquangulata and structural revision of quinquangulin and its glycosides: X.C. Li, et al.; J. Nat. Prod. 64, 1153 (2001)
- Antimycobacterial naphthopyrones from Senna oblique: J.G. Graham, et al.; J. Nat. Prod. 67, 225 (2004)
- Estrogenic and anti-estrogenic activities of Cassia tora phenolic constituents: A.M. El-Halawany, et al.; Chem. Pharm. Bull. (Tokyo) 55, 1476 (2007)
- In vitro cytotoxicity of fungal spoiling maize silage: R.R. Rasmussen, et al.; Food Chem. Toxicol. 49, 31 (2010)
- Three dimeric naphtho-γ-pyrones from the mangrove endophytic fungus Aspergillus tubingensis isolated from Pongamia pinnata: H.-B. Huang, et al.; Planta Med 76, 1888 (2010)
- Two novel classes of enzymes are required for the biosynthesis of aurofusarin in Fusarium graminearum: R.J.N. Frandsen, et al.; J. Biol. Chem. 286, 10419 (2011)
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