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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
polypeptide, sealed storage, away from moisture
- 英文名:
fMLP; N-Formyl-MLF
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
59880-97-6
- 规格:
5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 5 mg | 产品价格: | ¥500.0 |
|---|---|---|---|
| 规格: | 10 mg | 产品价格: | ¥800.0 |
| 规格: | 25 mg | 产品价格: | ¥1320.0 |
| 规格: | 50 mg | 产品价格: | ¥1900.0 |
| 规格: | 100 mg | 产品价格: | ¥2660.0 |
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N-Formyl-Met-Leu-Phe
CAS No. : 59880-97-6
MCE 国际站:N-Formyl-Met-Leu-Phe
产品活性:N-Formyl-Met-Leu-Phe (fMLP; N-Formyl-MLF) 是一种趋化肽和N-甲酰基肽受体 (FPR) 的特异性配体。报道显示N-Formyl-Met-Leu-Ph 可抑制 TNF-alpha 的分泌。
研究领域:Apoptosis
作用靶点:TNF Receptor
In Vitro: Binding of N-Formyl-Met-Leu-Phe to its specific cell surface receptor, N-formyl peptide receptor (FPR), triggers different cascades of biochemical events, eventually leading to cellular activation. FPR is a chemoattractant receptor belonging to the G protein-coupled receptor family. N-Formyl-Met-Leu-Phe promotes osteoblastic commitment and suppresses adipogenic commitment under osteoblastic differentiation conditions. N-Formyl-Met-Leu-Phe stimulates osteogenesis is associated with increased expression of osteogenic markers and mineralization. N-Formyl-Met-Leu-Phe inhibits expression of peroxisome proliferator-activated receptor-γ1. N-Formyl-Met-Leu-Phe-stimulated osteogenic differentiation is mediated via FPR1-phospholipase C/phospholipase D-Ca2+-calmodulin-dependent kinase II-ERK-CREB signaling pathways. N-Formyl-Met-Leu-Phe, a bacterial-derived peptide, induced proinflammatory cytokine gene expression in human peripheral blood monocytes. Bacterial products LPS and N-Formyl-Met-Leu-Phe synergistically induce inflammatory response via multiple signaling pathways. TLR4, IKKβ-IκBα, and NF-κB signaling pathways are involved in the synergistic induction of TNF-α via p65 nuclear translocation-dependent mechanisms.
In Vivo: N-Formyl-Met-Leu-Phe promotes bone formation in zebrafish and rabbits. Extensive skeletal development is evident at 5 dpf in over 80% of N-Formyl-Met-Leu-Phe-treated zebrafish. Treatment with N-Formyl-Met-Leu-Phe results in increased expression of Runx2. Bone marrow spaces are widely formed, and connective tissue covering bone is dense, like periosteum, in N-Formyl-Met-Leu-Phe-treated calvaria. N-Formyl-Met-Leu-Phe mediate release of calprotectin from PMN in vitro. It induces release of calprotectin from PMN in a dose dependent manner. A minimum of 10% of total PMN calprotectin is retained at concentrations of 0.1-10.0 nM of N-Formyl-Met-Leu-Phe.
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文献和实验)-Leu]的合成中,就使用了KH2PO4这样的弱碱催化,收率高达75%。用同样的方法合成Somatostatin的类似物Cyclo(Lys-Phe-D-Trp-Lys-Thy-Phe),收率也达到了42%。 以DPPA为缩合剂合成环肽时,有机碱常用三乙胺(Et3N)、N-甲基吗啉(NMM)和二异丙基乙胺(DIEA),这三种弱碱能够与有机溶剂混溶,用量远远少于NaHCO3和KH2PO4,而且NMM和DIEA不易引起消旋。 2.环肽合成中新型缩合剂 2.11-羟基-7-氮杂苯骈三唑(HOAt)衍生
Cysteine TGT,TGC D Asp Aspartic GAT,GAC E Glu Glutamic GAA,GAG F Phe Phenylalanine TTT,TTC G Gly Glycine GGT,GGC,GGA,GGG H His Histidine CAT,CAC I Ile Isoleucine ATT,ATC,ATA K Lys Lysine AAA,AAG L Leu Leucine TTG,TTA,CTT,CTC,CTA,CTG M Met Methionine ATG N
的。当蛋白N-端是Arg, Leu, Lys, Phe, Trp,或 Tyr这些氨基酸时,容易遭受蛋白酶降解,此即N-末端规则。N-端是Met时,大肠杆菌可以悄悄地把这个Met偷走,特别是Met后紧跟着一个带小侧链的氨基酸时。C-末端存在非极性氨基酸时,也容易导致蛋白被降解。C末端最后5个氨基酸是极性的或者带电荷的,则不易被降解。 6、二级翻译起始位点。这种情况见于你的序列里正好含有和核糖体结合位点完全一致的序列。那就怪不得人家了,核糖体会很高兴地找到这个位点,然后开始翻译,致使你的蛋白被截短
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