FC 131

Discontinued Product

4320 has been discontinued.

View all Chemokine CXC Receptors products.
Description: CXCR4 antagonist
Datasheet
Citations
Reviews
Literature (1)

Biological Activity for FC 131

CXCR4 antagonist (IC50 = 126 nM). Displays anti-HIV activity in assays using NL4-3 and IIIB strains (EC50 = 21 nM for both strains).

Technical Data for FC 131

M. Wt 729.84
Formula C36H47N11O6
Sequence XGYRR (Modifications: Cyclic peptide, X = 2-Nal, Tyr-3 = D-Tyr]
Storage Store at -20°C
CAS Number 606968-52-9
PubChem ID 5275848
InChI Key MBXBICVKLVYNKD-QUAHOIDUSA-N
Smiles NC(=N)NCCC[C@@H]1NC(=O)[C@@H](CC2=CC=C(O)C=C2)NC(=O)CNC(=O)[C@@H](CC2=CC3=CC=CC=C3C=C2)NC(=O)[C@H](CCCNC(N)=N)NC1=O

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

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

Product Datasheets for FC 131

Certificate of Analysis / Product Datasheet
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References for FC 131

References are publications that support the biological activity of the product.

Tamamura et al (2005) Stereoselective synthesis of [L-Arg-L/D-3-(2-naphthyl)alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogues of the CXCR4 antagonist FC131 J.Med.Chem. 48 380 PMID: 15658852

Inokuchi et al (2011) Potent CXCR4 antagonists containing amidine type peptide bond isosteres. ACS Med.Chem.Lett. 2 477

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View all Chemokine CXC Receptor Antagonists

Keywords: FC 131, FC 131 supplier, FC131, cxcr4, antagonists, chemokines, receptors, anti-HIV, Chemokine, CXC, Receptors, HIV, 4320, Tocris Bioscience

Citations for FC 131

Citations are publications that use Tocris products.

Currently there are no citations for FC 131.

Reviews for FC 131

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Literature in this Area

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

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Rheumatoid Arthritis Poster

Rheumatoid Arthritis Poster

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.