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Submit ReviewAMD 3465 hexahydrobromide is a potent, selective CXCR4 antagonist; exhibits 8-fold higher affinity than AMD 3100 (Cat.No. 3299). Inhibits SDF-1α-ligand binding (Ki = 41.7 nM). Potently inhibits HIV cell entry in vitro; causes leukocytosis and mobilizes haematopoietic stem cells in vivo.
AMD 3465 hexahydrobromide is also offered as part of the Tocriscreen 2.0 Max, Tocriscreen Antiviral Library and Tocriscreen Stem Cell Library. 了解 Tocris 化合物库的更多信息。
分子量 | 896.07 |
公式 | C24H38N6.6HBr |
储存 | Store at -20°C |
纯度 | ≥97% (HPLC) |
CAS Number | 185991-07-5 |
PubChem ID | 9897616 |
InChI Key | ARHBIBDGWDRBJH-UHFFFAOYSA-N |
Smiles | C1(CN3CCCNCCNCCCNCC3)=CC=C(CNCC2=NC=CC=C2)C=C1.Br.Br.Br.Br.Br.Br |
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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
water | 44.8 | 50 | |
DMSO | 22.4 | 25 |
以下数据基于产品分子量 896.07。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.5 mM | 2.23 mL | 11.16 mL | 22.32 mL |
2.5 mM | 0.45 mL | 2.23 mL | 4.46 mL |
5 mM | 0.22 mL | 1.12 mL | 2.23 mL |
25 mM | 0.04 mL | 0.22 mL | 0.45 mL |
参考文献是支持产品生物活性的出版物。
Rosenkilde et al (2007) Molecular mechanism of action of monocyclam versus bicyclam non-peptide antagonists of the CXCR4 chemokine receptor. J.Biol.Chem. 282 27354 PMID: 17599916
Bodart et al (2009) Pharmacology of AMD3465: A small molecule antagonist of the chemokine receptor CXCR4. Biochem.Pharmacol. 78 993 PMID: 19540208
If you know of a relevant reference for AMD 3465 hexahydrobromide, please let us know.
关键词: AMD 3465 hexahydrobromide, AMD 3465 hexahydrobromide supplier, AMD3465, CXCR4, receptor, antagonist, chemokine, chemokines, antagonists, Chemokine, CXC, Receptors, 4179, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 AMD 3465 hexahydrobromide 的部分引用包括:
Lourenco et al (2015) Macrophage migration inhibitory factor-CXCR4 is the dominant chemotactic axis in human mesenchymal stem cell recruitment to tumors. J Immunol 194 3463 PMID: 25712213
Luo et al (2016) Crosstalk between astrocytic CXCL12 and microglial CXCR4 contributes to the development of neuropathic pain. Mol Pain 12 PMID: 27030717
David L et al (2015) Identification of Therapeutic Targets of Inflammatory Monocyte Recruitment to Modulate the Allogeneic Injury to Donor Cornea. Invest Ophthalmol Vis Sci 56 7250-9 PMID: 26544793
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Receptor antagonists (SB225002: for CXCR2, AMD3465: for CXCR4, RS504393: for CCR2 and Maraviroc: for CCR5) at 10 μM
We ordered this product, combining with another inhibitor, to confirm the migration.To confirm that tested product induces migration, we also screen all MAPK inhibitors and MIF receptor antagonists
Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。
Rheumatoid arthritis (RA) is a chronic destructive inflammatory autoimmune disease that results from a breakdown in immune tolerance, for reasons that are as yet unknown. This poster summarizes the pathology of RA and the inflammatory processes involved, as well as describing some of the epigenetic modifications associated with the disease and the potential for targeting these changes in the discovery of new treatments.