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BioViotica
Averantin
As low as
CHF 95.00
In stock
Only %1 left
BVT-0169-M0011 mgCHF 95.00
BVT-0169-M0055 mgCHF 385.00
Specifications / Handling
| Product Details | |
|---|---|
| Synonyms | BRN 2309929; 2-(1-Hydroxyhexyl)-1,3,6,8-tetrahydroxyanthraquinone |
| Product Type | Chemical |
| Properties | |
| Formula |
C20H20O7 |
| MW | 372.4 |
| CAS | 5803-62-3 |
| Source/Host Chemicals | Isolated from Aspergillus sp. (strain WDMH51). |
| Purity Chemicals | ≥95% (HPLC; NMR) |
| Appearance | Orange powder. |
| Solubility | Soluble in acetone, methanol or DMSO. |
| Identity | Determined by 1H-NMR. |
| Declaration | Manufactured by BioViotica. |
| InChi Key | WGPOPPKSQRZUTP-LBPRGKRZSA-N |
| Smiles | CCCCC[C@H](O)C1=C(O)C2=C(C=C1O)C(=O)C1=C(C(O)=CC(O)=C1)C2=O |
| Shipping and Handling | |
| Shipping | AMBIENT |
| Short Term Storage | +4°C |
| Long Term Storage | -20°C |
| Handling Advice | Protect from light. |
| 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 |
Scientific Background Information
Product Description
- Mycotoxin.
- Intermediate of the biosynthetic pathway to aflatoxin B1.
- Cytotoxic against human solid tumor cell lines.
- Moderate antifungal and antibacterial agent.
Product-specific References
- Product B (Averantin), a pigment from Aspergillus versicolor: J.H. Birkinshaw, et al.; J. Chem. Soc. (C) 1966, 855 (1966)
- Stereochemical correlation of (-)-averantin: C.A. Townsend & S.B. Christensen; Tetrahedron Lett. 27, 887 (1986)
- A reappraisal of fungi producing aflatoxins: J. Varga: World Mycotoxin J. 2, 263 (2009)
- Bioactive metabolites from the sponge-derived fungus Aspergillus versicolor: Y.M. Lee, et. al; Arch. Pharm. Res. 33, 231 (2010)
- Genetics of polyketide metabolism in Aspergillus nidulans: M.L. Klejnstrup, et al.; Metabolites 2, 100 (2012)
- The antifungal metabolites obtained from the rhizospheric Aspergillus sp. YIM PH30001 against pathogenic fungi of Panax notoginseng: K. Liu, et al.; Nat. Prod. Res. 28, 2334 (2014)
- Polyketides and Meroterpenes from the Marine-Derived Fungi Aspergillus unguis 158SC-067 and A. flocculosus 01NT-1.1.5 and Their Cytotoxic and Antioxidant Activities: C.V. Anh, et al.; Mar. Drugs 19, 415 (2021)
- A Novel and Highly Efficient Microextraction Method for the Determination of Aflatoxin Precursor Averantin in Fatty Grain Samples: J. Li, et al.; J. Agric. Food Chem. 72, 1330 (2024)
- Genomic insights into the biosynthetic capacity of the sponge-associated fungus Aspergillus puulaauensis Hmp-F48: Y. Yan, et al.; BMC Genomics 27, 213 (2026)
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