Xanthomegnin

Bioviotica
Product Code: BVT-0365
Supplier: Bioviotica
CodeSizePrice
BVT-0365-C500500 ug£150.00
Quantity:
BVT-0365-M0011 mg£245.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
20°C
Storage:
-20°C

Images

1 / 1
Chemical Structure

Chemical Structure

Further Information

Alternate Names/Synonyms:
NSC264720
Appearance:
Orange crystalline solid.
CAS:
1685-91-2
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Hazards:
H302, H312, H319
InChi:
InChI=1S/C30H22O12/c1-9-5-11-7-13-17(23(33)15(11)29(37)41-9)25(35)19(27(39-3)21(13)31)20-26(36)18-14(22(32)28(20)40-4)8-12-6-10(2)42-30(38)16(12)24(18)34/h7-10,33-34H,5-6H2,1-4H3/t9-,10-/m1/s1
InChiKey:
WICHONPZVIYWIJ-NXEZZACHSA-N
Long Description:
Chemical. CAS: 1685-91-2. Formula: C30H22O12. MW: 574.5. Isolated from Penicillium citreo-viride. Genotoxic mycotoxin. Antitumor compound. Potent iNOS (NOSII) inhibitor. Interferes with cellular respiratory processes.
MDL:
MFCD00902622
Molecular Formula:
C30H22O12
Molecular Weight:
574.5
Package Type:
Plastic Vial
Precautions:
P270, P280, P301, P312, P302, P352, P312
Product Description:
Genotoxic mycotoxin. Antitumor and antiparasitic compound. Potent iNOS (NOSII) inhibitor. Interferes with cellular respiratory processes.
Purity:
>97% (HPLC)
Signal word:
Warning
SMILES:
COC1=C(C(=O)C2=C(C=C3C[C@@H](C)OC(=O)C3=C2O)C1=O)C1=C(OC)C(=O)C2=C(C(O)=C3C(=O)O[C@H](C)CC3=C2)C1=O
Solubility Chemicals:
Soluble in chloroform or DMSO; poorly soluble in methanol or water.
Source / Host:
Isolated 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) | Evaluation of the genotoxic activity of some mycotoxins using Escherichia coli in the SOS spot test: Y. Auffray & P. Boutibonnes; Mutat. Res. 171, 79 (1986) | Detection of xanthomegnin in epidermal materials infected with Trichophyton rubrum: A.K. Gupta, et al.; J. Invest. Dermatol. 115, 901 (2000) | Identification of inhibitors of inducible nitric oxide synthase from microbial extracts: A. A. Khisal et al.; J. Antibiot. 53, 496 (2000) | Xanthomegnin detection does not discriminate between Trichophyton rubrum and T. mentagrophytes complexes: H. Kandemir, et al.; J. Microbiol. Methods 111, 122 (2015) | Infrequent Production of Xanthomegnin by Fungal Strains Recovered from Patients with Ocular Mycoses: H. Ozdemir, et al.; Mycopathologia 181, 241 (2016)

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