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Cenicriviroc is an experimental drug candidate for the treatment of HIV infection.Cenicriviroc is an inhibitor of CCR2 and CCR5 receptors, allowing it to function as an entry inhibitor which prevents the virus from entering into a human cell.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 14.35 mL | 71.74 mL | 143.48 mL |
| 0.5 mM | 2.87 mL | 14.35 mL | 28.7 mL |
| 1 mM | 1.43 mL | 7.17 mL | 14.35 mL |
| 5 mM | 0.29 mL | 1.43 mL | 2.87 mL |
*The above data is based on the productmolecular weight 696.94. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Catalog Num | A13643 |
|---|---|
| Actions | Inhibitor |
| M. Wt | 696.94 |
| Formula | C41H52N4O4S |
| Solubility | DMSO |
| Purity | >98% |
| Storage | at -20°C 3 years Powder |
| CAS No. | 497223-25-3 |
| Synonyms | TAK-652, TBR-652 |
| SMILES | CCCCOCCOC1=CC=C(C=C1)C2=CC/3=C(C=C2)N(CCC/C(=C3)/C(=O)NC4=CC=C(C=C4)[[email protected]@](=O)CC5=CN=CN5CCC)CC(C)C |
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