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Emivirine

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Category Human immunodeficiency Virus (HIV)
CAS 149950-60-7
Description Emivirine (MKC-442) is a non-nucleoside reverse transcriptase inhibitors (NNRTIs) with Ki values of 0.20 and 0.01 μM for dTTP- and dGTP-dependent DNA or RNA polymerase activity, respectively. Emivirine displays potent and selective anti-human immunodeficiency virus type 1 (HIV-1) activity.
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Product Information

Synonyms Emivirine; Coactinon; MKC-442; I-EBU; 149950-60-7; 6-BENZYL-1-ETHOXYMETHYL-5-ISOPROPYLURACIL
IUPAC Name 6-benzyl-1-(ethoxymethyl)-5-propan-2-ylpyrimidine-2,4-dione
Molecular Weight 302.372
Molecular Formula C17H22N2O3
Canonical SMILES CCOCN1C(=C(C(=O)NC1=O)C(C)C)CC2=CC=CC=C2
InChI InChI=1S/C17H22N2O3/c1-4-22-11-19-14(10-13-8-6-5-7-9-13)15(12(2)3)16(20)18-17(19)21/h5-9,12H,4,10-11H2,1-3H3,(H,18,20,21)
InChIKey MLILORUFDVLTSP-UHFFFAOYSA-N
Purity 95%
Density 1.133g/cm3
Solubility In vitro:
10 mM in DMSO
Appearance Solid powder
Application Reverse Transcriptase Inhibitors
Storage Store at -20°C
Complexity 451
Exact Mass 302.16304257
In Vitro Emivirine (EMV) is also specific for HIV-1 RT and was without effect on HIV-2
Emivirine (EMV) has no obvious toxicity for human healthy cells
Cell Viability Assay
Cell Line: Human bone marrow cells collected from normal healthy volunteers
Concentration: 0, 0.1, 1, 10, or 100 μM
Incubation Time: 14 days
Result: At concentrations of 0.1 to 10 μM, no effect on cell growth, lactic acid production, mitochondrial DNA synthesis, or mitochondrial structure was seen compared to what occurred with untreated HepG2 cells.
In Vivo Tthe approximate lethal oral dose of Emivirine (EMV) for rats was ≥3 g/kg for males and 2.5 g/kg for females
PSA 64.09000
Target HIV
XLogP3-AA 2.6

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