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CXCR7 antagonist-1 hydrochloride
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Catalog No. T62325Cas No. 2990472-61-0
CXCR7 antagonist-1 hydrochloride is a CXCR7 antagonist that inhibits binding of SDF-1 chemokine (CXCL12 chemokine) or I-TAC to CXCR7, applicable for tumor and inflammation research.
CXCR7 antagonist-1 hydrochloride
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Purity: 99.84%
Catalog No. T62325Cas No. 2990472-61-0
CXCR7 antagonist-1 hydrochloride is a CXCR7 antagonist that inhibits binding of SDF-1 chemokine (CXCL12 chemokine) or I-TAC to CXCR7, applicable for tumor and inflammation research.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $189 | - | In Stock | |
| 5 mg | $479 | - | In Stock | |
| 10 mg | $793 | - | In Stock | |
| 25 mg | $1,570 | - | In Stock | |
| 50 mg | $2,650 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $528 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.84%
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Product Introduction
Bioactivity
Chemical Properties
| Description | CXCR7 antagonist-1 hydrochloride is a CXCR7 antagonist that inhibits binding of SDF-1 chemokine (CXCL12 chemokine) or I-TAC to CXCR7, applicable for tumor and inflammation research. |
| In vitro | CXCR7 antagonist-1 hydrochloride (10 μM; 48 h) restored β2-adrenergic receptor (β2AR) downregulation and muscle relaxation in infant airway smooth muscle cells induced by CXCL11 or RSV infection [2]. |
| In vivo | CXCR7 antagonist-1 hydrochloride (10 μM; intranasal instillation; once daily; administered twice) suppressed RSV infection-induced airway smooth muscle relaxation in a BALB/c mouse model [2]. |
| Molecular Weight | 426.87 |
| Formula | C21H20ClFN6O |
| Cas No. | 2990472-61-0 |
| Smiles | N(C(=O)C1=NN(C=C1)C2=CC=C(F)C=C2)[C@@H]3CN(C=4C=5N(C=CN4)C=CC5)CC3.Cl |
| Color | Gray |
| Appearance | Solid |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 300 mg/mL (702.79 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
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Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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