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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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R126706-1mg | 1mg | In stock | $35.90 | |
R126706-5mg | 5mg | In stock | $147.90 | |
R126706-25mg | 25mg | In stock | $494.90 | |
R126706-100mg | 100mg | In stock | $1,782.90 |
Synonyms | [D-Pen2,5]Enkephalin | Repertaxin;DF 1681Y | CS-1379 | DTXSID6046509 | L-Arginyl-Glycyl-L-Aspartic acid | Bio1_000853 | HY-15251 | (+-)-Diethyl (1-(3-(2-chloroethyl)-3-nitrosoureido)ethyl)phosphonate | Q27088533 | s8640 | (2R)-2-(4-(2-Methylpropyl)phenyl) |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | The efficacy of RPX (tested in a wide range of concentrations (1-1000 nM)) was lower in cells expressing Ile43Val CXCR1 mutant (IC50 values of 0.0056 and 0.08 uM for CXCR1 weight and CXCR1 Ile43Val, respectively). Treatment with reparixin significantly c |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | ALLOSTERIC MODULATOR, MODULATOR |
Mechanism of action | Interleukin-8 receptor B modulator |
Product Description | Reparixin(DF 1681Y) is an inhibitor of CXCL8 receptor, also inhibit CXCR1 and CXCR2 activation, which has been shown to attenuate inflammatory responses in various injury models. |
ALogP | 2.9 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | (2R)-2-[4-(2-methylpropyl)phenyl]-N-methylsulfonylpropanamide |
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INCHI | InChI=1S/C14H21NO3S/c1-10(2)9-12-5-7-13(8-6-12)11(3)14(16)15-19(4,17)18/h5-8,10-11H,9H2,1-4H3,(H,15,16)/t11-/m1/s1 |
InChi Key | KQDRVXQXKZXMHP-LLVKDONJSA-N |
Canonical SMILES | CC(C)CC1=CC=C(C=C1)C(C)C(=O)NS(=O)(=O)C |
Isomeric SMILES | C[C@H](C1=CC=C(C=C1)CC(C)C)C(=O)NS(=O)(=O)C |
PubChem CID | 9838712 |
Molecular Weight | 283.39 |
PubChem CID | 9838712 |
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ChEMBL Ligand | CHEMBL191413 |
CAS Registry No. | 266359-83-5 |
GPCRdb Ligand | reparixin |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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I2130052 | Certificate of Analysis | Jul 07, 2023 | R126706 |
I2130053 | Certificate of Analysis | Jul 07, 2023 | R126706 |
I2130054 | Certificate of Analysis | Jul 07, 2023 | R126706 |
I2130055 | Certificate of Analysis | Jul 07, 2023 | R126706 |
Solubility | 25°C: DMSO |
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Specific Rotation[α] | (α/D -80 to -90°, c = 1.0 in ethanol) |
Pictogram(s) | GHS07 |
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Signal | Warning |
Hazard Statements | H302:Harmful if swallowed |
Precautionary Statements | P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P330:Rinse mouth. P301+P317:IF SWALLOWED: Get medical help. |
1. Bertini R, Allegretti M, Bizzarri C, Moriconi A, Locati M, Zampella G, Cervellera MN, Di Cioccio V, Cesta MC, Galliera E et al.. (2004) Noncompetitive allosteric inhibitors of the inflammatory chemokine receptors CXCR1 and CXCR2: prevention of reperfusion injury.. Proc Natl Acad Sci USA, 101 (32): (11791-6). [PMID:15282370] [10.1021/op500134e] |
2. Maffi P, Lundgren T, Tufveson G, Rafael E, Shaw JAM, Liew A, Saudek F, Witkowski P, Golab K, Bertuzzi F et al.. (2020) Targeting CXCR1/2 Does Not Improve Insulin Secretion After Pancreatic Islet Transplantation: A Phase 3, Double-Blind, Randomized, Placebo-Controlled Trial in Type 1 Diabetes.. Diabetes Care, 43 (4): (710-718). [PMID:32019854] [10.1021/op500134e] |
3. Goldstein LJ, Perez RP, Yardley D, Han LK, Reuben JM, Gao H, McCanna S, Butler B, Ruffini PA, Liu Y et al.. (2020) Correction to: A window-of-opportunity trial of the CXCR1/2 inhibitor reparixin in operable HER-2-negative breast cancer.. Breast Cancer Res, 22 (1): (52). [PMID:32434589] [10.1021/op500134e] |