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BioViotica
Cladospirone bisepoxide
155
CHF
CHF 155.00
In stock
BVT-0065-M0011 mgCHF 155.00
Product Details | |
---|---|
Synonyms | Palmarumycin C13; Diepoxin ζ; Antibiotic Sch53514 |
Product Type | Chemical |
Properties | |
Formula |
C20H14O7 |
MW | 366.3 |
CAS | 152607-03-9 and 155866-40-3 |
Source/Host Chemicals | Isolated from Sphaeropsidales sp. |
Purity Chemicals | ≥98% (HPLC) |
Appearance | White to off-white solid. |
Solubility | Soluble in DMSO or methanol:dimethylformamide (1:1). |
Identity | Determined by 1H-NMR. |
Declaration | Manufactured by BioViotica. |
InChi Key | AUWGMDYISSBOED-CCNMWVGKSA-N |
Smiles | O[C@H]1C=CC(=O)[C@]23O[C@]12[C@@H](O)[C@H]1O[C@H]1C31OC2=CC=CC3=CC=CC(O1)=C23 |
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
- Antibiotic.
- Antibacterial and antifungal.
- Antitumor compound.
- Germination inhibitor.
Product References
- Diepoxins, Novel Fungal Metabolites with Antibiotic Activity: G. Schlingmann, et al.; Tetrahedr. Lett. 34, 7225 (1993)
- Production of cladospirone bisepoxide, a new fungal metabolite: F. Petersen, et al.; J. Antibiot. 47, 1098 (1994)
- A novel class of antitumor metabolites from the fungus Naitrassia mangiferae: M. Chu, et al.; Tetrahedr. Lett. 35, 1343 (1994)
- Biosynthesis of cladospirone bisepoxide, a member of the spirobisnaphthalene family: H.B. Bode, et al.; J. Antibiot. 53, 153 (2000)
- UV mutagenesis and enzyme inhibitors as tools to elucidate the late biosynthesis of the spirobisnaphthalenes: H.B. Bode & A. Zeeck; Phytochemistry 55, 311 (2000)
- Big effects from small changes: possible ways to explore nature's chemical diversity: H.B. Bode, et al.; Chembiochem 3, 619 (2002)
- Natural products derived from naphthalenoid precursors by oxidative dimerization: K. Krohn; Prog. Chem. Org. Nat. Prod. 85, 1-49 (2003) (Review)
- Spirobisnaphthalenes from the endophytic fungus Dzf12 of Dioscorea zingiberensis and their antimicrobial activities: X. Cai, et al.; Nat. Prod. Commun. 4, 1469 (2009)