Cas No.: | 854755-48-9 |
Synonyms: | CHEMBL470508, A-790742,A790742,A 790742 |
SMILES: | O=C(OC)N[C@H](C(N[C@H](CC1=CC=C(C2=NC=CC=C2)C=C1)C[C@H](O)[C@@H](NC([C@@H](N3CCN(CC4=NC(C(C)(O)C)=CC=C4)C3=O)C(C)(C)C)=O)CC5=CC=CC=C5)=O)C(C)(C)C |
Formula: | C49H65N7O7 |
M.Wt: | 864.0831 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | A-790742 is a potent human immunodeficiency virus type 1 (HIV-1) protease inhibitor, with 50% effective concentrations ranging from 2 to 7 nM against wild-type HIV-1. The activity of this compound is lowered by approximately sevenfold in the presence of 50% human serum. A-790742 maintained potent antiviral activity against lopinavir-resistant variants generated in vitro as well as against a panel of molecular clones containing proteases derived from HIV-1 patient isolates with multiple protease mutations. During in vitro selection, A-790742 selected two primary mutations (V82L and I84V) along with L23I, L33F, K45I, A71V/A, and V77I in the pNL4-3 background and two other mutations (A71V and V82G) accompanied by M46I and L63P in the HIV-1 RF background. HIV-1 pNL4-3 clones with a single V82L or I84V mutation were phenotypically resistant to A-790742 and ritonavir. A-790742 displays a favorable anti-HIV-1 profile against both the wild type and a large number of mutants resistant to other protease inhibitors. . For the detailed information of A-790742, the solubility of A-790742 in water, the solubility of A-790742 in DMSO, the solubility of A-790742 in PBS buffer, the animal experiment (test) of A-790742, the cell expriment (test) of A-790742, the in vivo, in vitro and clinical trial test of A-790742, the EC50, IC50,and affinity,of A-790742, Please contact DC Chemicals. |