F1147

Fumonisin B₁ from Fusarium moniliforme

≥98% (HPLC)

• Sinônimo(s): Macrofusine
• Fórmula empírica (Notação de Hill): C₃₄H₅₉NO₁₅
• Número CAS: 116355-83-0
• Peso molecular: 721.83
• Número MDL: MFCD27977580
• Código UNSPSC: 12352200
• ID de substância PubChem: 24894752
• NACRES: NA.32

Propriedades

• fonte biológica: Fusarium sp. (Fusarium moniliforme)
• Nível de qualidade: 300
• Ensaio: ≥98% (HPLC)
• Formulário: powder
• solubilidade: methanol: 9.80-10.20 mg/mL, clear, colorless to light yellow
• temperatura de armazenamento: 2-8°C
• cadeia de caracteres SMILES: CCCC[C@@H](C)[C@@H](OC(=O)C[C@@H](CC(O)=O)C(O)=O)[C@H](C[C@@H](C)C[C@H](O)CCCC[C@@H](O)C[C@H](O)[C@H](C)N)OC(=O)C[C@@H](CC(O)=O)C(O)=O
• InChI: 1S/C34H59NO15/c1-5-6-9-20(3)32(50-31(44)17-23(34(47)48)15-29(41)42)27(49-30(43)16-22(33(45)46)14-28(39)40)13-19(2)12-24(36)10-7-8-11-25(37)18-26(38)21(4)35/h19-27,32,36-38H,5-18,35H2,1-4H3,(H,39,40)(H,41,42)(H,45,46)(H,47,48)/t19-,20+,21-,22+,23+,24+,25+,26-,27-,32+/m0/s1
• chave InChI: UVBUBMSSQKOIBE-DSLOAKGESA-N

Descrição

Descrição geral

Fumonisin B1 is a mycotoxin found in many Fusarium fungi, such as Fusarium moniliforme, Fusarium proliferatum, and Fusarium verticillioides. This toxin can also be found in feedstocks and food stocks, such as corn / maize, that have been infected with Fusarium.

Fumonisin B1 (FB1) shares structure similarities with sphingosine. Thus fumonisin B1 can inhibit ceramide synthase (sphingosine N-acetyltransferase), which can lead to disruption of ceramide biosynthesis and complex sphingolipid biosynthesis.

Aplicação

Fumonisin B1 from Fusarium moniliforme has been used:

• as a standard in the analysis of mycotoxins in caecal content obtained from adult pigs
• in the study of the effect of fumonisin B1 on the metabolism of prion protein (PrP) isoforms and the synthesis of scrapie prion protein PrP^Sc and
• in the study of the toxic effects of fumonisin B1 on explants obtained from pig jejunum.

Ações bioquímicas/fisiológicas

Fumonisin B1 acts as a hepatocarcinogen and causes hepatotoxicity in rats. In horses, it causes leukoencephalitis, and in pigs, it causes pulmonary edema syndrome. In China and southern parts of Africa, it is linked with high incidence of esophageal cancer in humans. It acts as an inhibitor of sphingosine N-acyltransferase enzyme (ceramide synthase), related to structural similarities between fumonisin B1 and sphingoid bases like sphingosine.

Fungal metabolite believed to cause leukoencephalomalacia in horses.

Informações de segurança

• Pictogramas: GHS06,GHS08
• Palavra indicadora: Danger
• Frases de perigo: H301,H351,H361d,H373
• Declarações de precaução: P202 - P260 - P264 - P280 - P301 + P310 - P405
• Classificações de perigo: Acute Tox. 3 Oral - Carc. 2 - Repr. 2 - STOT RE 2
• Órgãos-alvo: Kidney,Liver
• Código de classe de armazenamento: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable
• Equipamento de proteção individual: Eyeshields, Gloves, type P3 (EN 143) respirator cartridges