FSLLRY-NH2

Pricing Availability   Qty
说明: PAR2 peptide antagonist
纯度: ≥95% (HPLC)
说明书
引用文献 (9)
评论

生物活性 for FSLLRY-NH2

FSLLRY-NH2 is a selective PAR2 peptide antagonist. Reverses taxol-induced mechanical allodynia, heat hyperalgesia and PKC activation in ICR mice. Blocks ERK activation and collagen production in isolated cardiac fibroblasts. Also reduces symptoms in a mouse model of dermatophyte-associated itch. FSLLRY-NH2 inhibits C. albicans induced inflammation in oral mucosal cells in vitro.

技术数据 for FSLLRY-NH2

分子量 796.97
公式 C39H60N10O8
序列 FSLLRY

(Modifications: Tyr-6 = C-terminal amide)

储存 Store at -20°C
纯度 ≥95% (HPLC)
CAS Number 245329-02-6
PubChem ID 73352412
InChI Key KMSCNWHRNILNRJ-JNRWAQIZSA-N
Smiles [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(N)=O

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for FSLLRY-NH2

溶解性 Soluble to 1 mg/ml in water

产品说明书 for FSLLRY-NH2

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关键词: FSLLRY-NH2, FSLLRY-NH2 supplier, PAR2, protease, activated, receptors, selective, antagonists, Protease-Activated, Receptors, 4751, Tocris Bioscience

9 篇 FSLLRY-NH2 的引用文献

引用文献是使用了 Tocris 产品的出版物。 FSLLRY-NH2 的部分引用包括:

White et al (2015) A brief exposure to tryptase or thrombin potentiates fibrocyte differentiation in the presence of serum or serum amyloid P. Cell Death Dis 194 142 PMID: 25429068

Bao et al (2014) PAR2-mediated upregulation of BDNF contributes to central sensitization in bone cancer pain. Mol Pain 10 28 PMID: 24886294

Tripathi et al (2014) Protease-activated receptor 2 (PAR2) is upregulated by Acanthamoeba plasminogen activator (aPA) and induces proinflammatory cytokine in human corneal epithelial cells. Invest Ophthalmol Vis Sci 55 3912 PMID: 24876278

Eum et al (2014) Disruption of epithelial barrier by quorum-sensing N-3-(oxododecanoyl)-homoserine lactone is mediated by matrix metalloproteinases. Am J Physiol Gastrointest Liver Physiol 306 G992 PMID: 24742991


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