(R)-Semixanthomegnin
| Code | Size | Price |
|---|
| BVT-0366-C500 | 500 ug | £145.00 |
Quantity:
| BVT-0366-M001 | 1 mg | £235.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
-20°C
Documents
Further Information
Appearance:
Orange crystalline solid.
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.
Hazards:
H302, H312, H319
InChi:
InChI=1S/C15H12O6/c1-6-3-7-4-8-12(14(18)11(7)15(19)21-6)9(16)5-10(20-2)13(8)17/h4-6,18H,3H2,1-2H3/t6-/m1/s1
InChiKey:
YPJWDOQDLYENRC-ZCFIWIBFSA-N
Long Description:
Chemical. Formula: C15H12O6. MW: 288.3. Derivative of semivioxanthin from Penicillium citreo-viride. Antibacterial mycotoxin derivative. Monomer (half) of the genotoxic mycotoxin xanthomegnin.
Molecular Formula:
C15H12O6
Molecular Weight:
288.3
Package Type:
Plastic Vial
Precautions:
P270, P280, P301, P312, P302, P352, P312
Product Description:
Antibacterial mycotoxin derivative. Monomer (half) of the genotoxic mycotoxin xanthomegnin.
Purity:
>97% (HPLC)
Signal word:
Warning
SMILES:
COC1=CC(=O)C2=C(O)C3=C(C[C@@H](C)OC3=O)C=C2C1=O
Solubility Chemicals:
Soluble in chloroform or DMSO. Poorly soluble in methanol or water.
Source / Host:
Derivative of semivioxanthin from Penicillium citreo-viride.
Transportation:
Non-hazardous
UNSPSC Category:
Natural Products/Extracts
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 1 year after receipt when stored at -20°C. After reconstitution protect from light at -20°C.
References
Isolierung des Antibioticums semi-Vioxanthin aus Penicillium citreo-viride und Synthese des Xanthomegnins: A. Zeeck, et al.; Chem. Ber. 112, 957 (1979) | Toxicity, mutagenicity and tetragenicity of Brevianamide, Viomellein and Xanthomegnin; secondary metabolites of Penicillium viridicatum: A.J. Delucca, et al.; J. Food Safety 4, 165 (1982) | Total synthesis of (R)-semixanthomegnin and the x-ray crystal structure of (?)-7-chloro-10-methoxy-3-methyl-3,4-dihydro-1H-naphtho[2,3-c]pyran-1,6,9-trione: A.S. Cotterill, et al.; Aust. J. Chem. 56, 49 (2003) | Synthesis of pyran and pyranone natural products: Christopher D. Donner, et al.; Molecules 9, 498 (2004)
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