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Synonyms:
BNM-III-170 free base
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | BNM-III-170 free base is a CD4 mimetic compound that acts as an anti-HIV-1 agent. It binds to the Phe43 cavity on HIV-1 gp120, inhibiting the virus's entry into target cells, making it useful for research related to HIV-1 infection. |
| In vitro | BNM-III-170 free base inhibits the entry of the HIV-1 JR FL strain into Cf2Th CD4/CCR5 cells with an IC50 of 14.5 μM. It exhibits inhibitory effects against various HIV-1 strains, with an IC50 range of 9-200 μM. |
| Molecular Weight | 446.91 |
| Formula | C21H24ClFN6O2 |
| Cas No. | 1859189-54-0 |
| Smiles | N(C(C(NC1=CC(F)=C(Cl)C=C1)=O)=O)[C@H]2C=3C(C[C@@H]2CNC(=N)N)=CC(CNC)=CC3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
| Size | Quantity | Unit Price | Amount | Operation |
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