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- 文献和实验
- 技术资料
- 保存条件:
Powder: -80°C, 2 years; -20°C, 1 year. In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名:
Fmoc-Thr(Ac₃AcNH-α-Gal)-OH
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
25 mg/50 mg/100 mg
| 规格: | 25 mg | 产品价格: | ¥2950.0 |
|---|---|---|---|
| 规格: | 50 mg | 产品价格: | ¥5200.0 |
| 规格: | 100 mg | 产品价格: | ¥8100.0 |
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Fmoc-Thr[GalNAc(Ac)3-α-D]-OH
CAS No. : 116783-35-8
MCE 国际站:Fmoc-Thr[GalNAc(Ac)3-α-D]-OH
产品活性:Fmoc-Thr[GalNAc(Ac)3-α-D]-OH 是用于研究制备癌症疫苗的结构单元。
研究领域:Others
作用靶点:Others
In Vitro: The O-glycosidic linkage and the O-acetyl protection in this building block is stable to both piperidine and TFA, making it completely compatible with standard protocols in Fmoc solid phase peptide synthesis. The Tn antigen is a tumor-associated carbohydrate antigen that is not normally expressed in peripheral tissues or blood cells. Expression of this antigen, which is found in a majority of human carcinomas of all types, arises from a blockage in the normal O-glycosylation pathway in which glycans are extended from the common precursor GalNAcα1-O-Ser/Thr (Tn +antigen). This precursor is generated in the Golgi apparatus on newly synthesized glycoproteins by a family of polypeptide α- N-acetylgalactosaminyltransferases (ppGalNAcTs) and then extended to the common core 1 O-glycan Galβ1-3GalNAcα1-OSer/Thr (T antigen) by a single enzyme termed the T-synthase (core 1 β3-galactosyltransferase or C1GalT). Formation of the active form of the T-synthase requires a unique molecular chaperone termed Cosmc, encoded by Cosmc on the X-chromosome.
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文献和实验Characterization of Protein Glycosylation
(A) There are two alternative forms for portraying monosaccharides as shown here for β- D - N -acetylglucosamine (GlcNAc). Different monosaccharides vary by the number and orientation of then functional groups, i.e., OH, NHAc, and the like Compared to GlcNAc, GalNAc has the C
phosphorylation)和单体法(Building block approach),如Figure 2所示。前者是在多肽序列合成结束后再在固相载体上对丝氨酸、苏氨酸或酪氨酸的侧链羟基进行磷酸化,可以在同一次合成中同时得到带有和不带有磷酸化位点的多肽;而后者则将适当保护的磷酸化氨基酸直接引入到多肽序列中,操作较前者更为简单,现已成为磷酸化多肽合成的首选策略。 在采用单体法构建磷酸化多肽时,目前广泛采用的原料为侧链单苄基保护的氨基酸:Fmoc-AA(PO(OBzl)OH)-OH (AA = Ser, Thr
为缩合剂,保持pH 8.5~9,反应4天,得到相应的环六肽和环五肽,收率在15%~50%之间。生物活性实验表明所有的环六肽对细胞粘附的抑制作用均明显低于线性肽GRGDS。环五肽中也只有Cyclo(RGDdFV)和Cyclo(RGDFd-V)对Laminin P1的细胞粘附具有明显的抑制作用。 对于某些在碱性条件下易分解的目的物,反应过程当中应用惰性气体进行保护,例如,线性多肽H-Asp(Fmoc)- d-Ser-Phe- D-Phe- Arg- Gly - OH在无水DMF中,加入5倍量NaHCO
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