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包装 1mg | 5mg
纯度 ≥98% (HPLC)
发货地 现货 品牌 阿拉丁
最小起订 1MG
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产品详情

中文名称 别名
CasNo 116355-83-0 产品类别 化学和生化试剂,生化试剂,生物制药生产,制剂,固体制剂

产品名称

英文名称:Fumonisin B1

同义词

fumonisin b1、116355-83-0、fumonisin-B1、Macrofusine、1,2,3-Propanetricarboxylic acid, 1,1'-[(1S,2R)-1-[(2S,4R,9R,11S,12S)-12-amino-4,9,11-trihydroxy-2-methyltridecyl]-2-[(1R)-1-methylpentyl]-1,2-ethanediyl] ester, (2R,2'R)-、3ZZM97XZ32、fumonisin B(1)、FB1、(R)-、烟曲霉毒素 B1

产品性质

CAS编号:116355-83-0

分子式:C34H59NO15

分子量:721.83

PubChem编号:2733487

别名:烟曲霉毒素 B1

英文别名:fumonisin b1|116355-83-0|fumonisin-B1|Macrofusine|1,2,3-Propanetricarboxylic acid, 1,1'-[(1S,2R)-1-[(2S,4R,9R,11S,12S)-12-amino-4,9,11-trihydroxy-2-methyltridecyl]-2-[(1R)-1-methylpentyl]-1,2-ethanediyl] ester, (2R,2'R)-|3ZZM97XZ32|fumonisin B(1)|FB1|(R)-

规格或纯度:≥98% (HPLC)

英文名称:Fumonisin B1

生化机理:真菌代谢物,可引起马脑白质软化症。霉菌毒素和蛋白丝氨酸/苏氨酸磷酸酶抑制剂(IC 50值为80μM(PP5),0.3(PP2Cα),0.4(PP2A),0.5(PP1γ2)和3 mM(PP2B))。细胞增殖抑制剂和凋亡诱导剂。

储存温度:-20°C储存,充氩

运输条件:超低温冰袋运输

备注:如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。

产品介绍:Fumonisin B1 is a fungal metabolite produced by Fusarium moniliforme, that has been shown to inhibit protein serine/threonine phosphatases (PP1, PP2A, PP2B, PP2C, and PP5/T/K/H), and is most effective with PP5. It has been shown to stimulate the activation of mitogen-activated protein kinase. Fumonisin B1 has been observed to inhibit sphingolipid biosynthesis, preferentially inhibiting sphingomyelin biosynthesis versus glycosphingolipids in neuronal cells. In primary rat liver cells, fumonisin B1 blocked biosynthesis of de novo sphingolipids throμgh LASS (ceramide synthase) inhibition. Caspase-3 activated or DNA fragmented apoptosis induced by fumonisin B1 binding to a TNF receptor has been documented in many human and rat cell lines. Fumonisin B1 has displayed immunotoxic effects by increasing expression of IL-1β, TNFα, IFN-γ; (interferon γ), IL-1α, IL-6, IL-10, IL-18 and IL-12 in varying mouse cells. Immunotoxicity of fumonisin B1 in human dendritic cells has been demonstrated throμgh expression of chemokine CXCL9 and IFN-γ. Further, fumonisin B1 is an activator of Akt.A serine/threonine phosphatase inhibitor.Fumonisin B1 is a fungal metabolite produced by Fusarium moniliforme, that has been shown to inhibit protein serine/threonine phosphatases (PP1, PP2A, PP2B, PP2C, and PP5/T/K/H), and is most effective with PP5. It has been shown to stimulate the activation of mitogen-activated protein kinase. Fumonisin B1 has been observed to inhibit sphingolipid biosynthesis, preferentially inhibiting sphingomyelin biosynthesis versus glycosphingolipids in neuronal cells. In primary rat liver cells, fumonisin B1 blocked biosynthesis of de novo sphingolipids through LASS (ceramide synthase) inhibition. Caspase-3 activated or DNA fragmented apoptosis induced by fumonisin B1 binding to a TNF receptor has been documented in many human and rat cell lines. Fumonisin B1 has displayed immunotoxic effects by increasing expression of IL-1β, TNFα, IFN-γ; (interferon γ), IL-1α, IL-6, IL-10, IL-18 and IL-12 in varying mouse cells. Immunotoxicity of fumonisin B1 in human dendritic cells has been demonstrated through expression of chemokine CXCL9 and IFN-γ. Further, fumonisin B1 is an activator of Akt.A serine/threonine phosphatase inhibitor.

IUPAC Name:(2R)-2-[2-[(5R,6R,7S,9S,11R,16R,18S,19S)-19-amino-6-[(3R)-3,4-dicarboxybutanoyl]oxy-11,16,18-trihydroxy-5,9-dimethylicosan-7-yl]oxy-2-oxoethyl]butanedioic acid

INCHI: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

InChi Key:UVBUBMSSQKOIBE-DSLOAKGESA-N

Canonical SMILES:CCCCC(C)C(C(CC(C)CC(CCCCC(CC(C(C)N)O)O)O)OC(=O)CC(CC(=O)O)C(=O)O)OC(=O)CC(CC(=O)O)C(=O)O

Isomeric SMILES:CCCC[C@@H](C)[C@H]([C@H](C[C@@H](C)C[C@@H](CCCC[C@H](C[C@@H]([C@H](C)N)O)O)O)OC(=O)C[C@@H](CC(=O)O)C(=O)O)OC(=O)C[C@@H](CC(=O)O)C(=O)O

WGK Germany:3

RTECS:TZ8350000

PubChem CID:2733487

溶解性:Soluble in water (25 mg/mL), methanol (10 mg/mL), acetonitrile, and DMSO (10 mM).

敏感性:对光线和湿度敏感

象形图:

信号词:Warning

危险声明:H351 Suspected of causing cancer

预防措施声明:P280,P405,P501,P203,P318

个人防护装备:Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges

产品包装

纯度包装库存所在地
≥98% (HPLC)1mg现货
≥98% (HPLC)5mg现货
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