21 Results for "

efavirenz

" in MedChemExpress (MCE) Product Catalog:
Products (21)

21 Results for "efavirenz" in MCE Product Catalog:

17
17 Cited Publications
Art. -Nr.: HY-10572
CAS. Nr.: 154598-52-4
Reinheit:  99.93%
Synonyms: DMP 266; EFV; L-743726
Efavirenz (DMP 266) is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a Ki of 2.93 nM and exhibits an IC95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture .
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Art. -Nr.: HY-137397
CAS. Nr.: 205754-33-2
Reinheit:  97.00%
Synonyms: 8-OH-EFV
Target:  

Apoptosis JNK

Forschungsgebiete:  

Cancer

8-Hydroxyefavirenz (8-OH-EFV) is a primary metabolite of (HY-10572). 8-Hydroxyefavirenz induces apoptosis via a JNK- and BimEL-dependent mechanism in primary human hepatocytes. 8-Hydroxyefavirenz can be used in research of cancer . 8-Hydroxyefavirenz is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Art. -Nr.: HY-14891
CAS. Nr.: 1018450-26-4
Reinheit:  98.96%
Synonyms: GSK2248761; FDV
Forschungsgebiete:  

Infection

Fosdevirine (GSK2248761) is is a potent, selective, non-nucleoside reverse transcriptase inhibitor (NNRTI) of human immunodeficiency virus type 1 (HIV-1) replication with low nanomolar activity in vitro. Fosdevirine shows good activity against a broad range of HIV-1 strains, including efavirenz (HY-10572)-resistant clinical isolates .
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Art. -Nr.: HY-10572S
CAS. Nr.: 1132642-95-5
Efavirenz-d5 (DMP 266-d5) is the deuterium labeled Efavirenz. Efavirenz (DMP 266) is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a Ki of 2.93 nM and exhibits an IC95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture . Efavirenz-d5 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Art. -Nr.: HY-131422S
CAS. Nr.: 1246812-30-5
rac 8-Hydroxy Efavirenz-d4 is the deuterium labeled rac 8-Hydroxy Efavirenz . rac 8-Hydroxy Efavirenz-d4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Art. -Nr.: HY-10572R
CAS. Nr.: 154598-52-4
Synonyms: DMP 266 (Standard); EFV (Standard); L-743726 (Standard)
Efavirenz (Standard) is the analytical standard of Efavirenz. This product is intended for research and analytical applications. Efavirenz (DMP 266) is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a Ki of 2.93 nM and exhibits an IC95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture .
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Art. -Nr.: HY-10572B
CAS. Nr.: 177530-93-7
Synonyms: (Rac)-DMP 266; (Rac)-EFV; (Rac)-L-743726
(Rac)-Efavirenz is the isomer of Efavirenz (HY-10572). Efavirenz (DMP 266) is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a Ki of 2.93 nM and exhibits an IC95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture .
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Art. -Nr.: HY-10572A
CAS. Nr.: 154801-74-8
Synonyms: (R)-DMP 266; (R)-EFV; (R)-L-743726
Target:  

Reverse Transcriptase

Forschungsgebiete:  

Infection

(R)-Efavirenz ((R)-DMP 266) is a non-nucleoside reverse transcriptase inhibitor that acts by non-competitive inhibition of the viral enzyme. (R)-Efavirenz can be metabolized by CYP2B6 to 8-hydroxyefavirenz in a highly stereoselective manner. (R)-Efavirenz is promising to be a useful probe for the CYP2B6 active site and catalytic mechanisms .
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Art. -Nr.: HY-10572S1
CAS. Nr.: 1261394-62-0
Synonyms: DMP 266-13C6; EFV-13C6; L-743726-13C6
Efavirenz- 13C6 is the 13C-labeled Efavirenz. Efavirenz (DMP 266) is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a Ki of 2.93 nM and exhibits an IC95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture .
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Art. -Nr.: HY-131422
CAS. Nr.: 205754-32-1
Target:  

Drug Metabolite

Forschungsgebiete:  

Infection

(Rac)-8-Hydroxy-efavirenz is a metabolite of Efavirenz (HY-10572), a non-nucleoside HIV-1 reverse transcriptase inhibitor .
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Art. -Nr.: HY-123330
CAS. Nr.: 457635-65-3
Forschungsgebiete:  

Infection

GW695634 is an orally active prodrug of GW678248. GW695634 undergoes amidolysis in vivo to release the active ingredient GW678248, thereby inhibiting viral replication. GW678248 is a non-nucleoside reverse transcriptase inhibitor (NNRTi) with potent antiviral activity against Efavirenz (HY-10572)-resistant and Nevirapine (HY-10570)-resistant HIV and AIDS viruses .
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Art. -Nr.: HY-10572BS1
CAS. Nr.: 2749807-27-8
(Rac)-Efavirenz-d5 is deuterium labeled (Rac)-Efavirenz. (Rac)-Efavirenz-d5 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Art. -Nr.: HY-10572BS
CAS. Nr.: 1246812-58-7
(Rac)-Efavirenz-d4 is a labelled racemic Efavirenz. Efavirenz (DMP 266) is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a Ki of 2.93 nM and exhibits an IC95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture . (Rac)-Efavirenz-d4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Art. -Nr.: HY-19869
CAS. Nr.: 878670-89-4
Forschungsgebiete:  

Infection

VRX-480773 is an efficient non-nucleoside reverse transcriptase inhibitor (NNRTI), used for HIV infection. VRX-480773 has high specificity for HIV-1, with an EC50 for wild-type HIV-1 being 0.14 nM. VRX-480773 does not inhibit HIV-2, HBV or HCV, and has no effect on human DNA polymerase α/β. VRX-480773 retains inhibitory activity against Efavirenz (HY-10572) resistant strains, with EC50s mostly < 1 nM. VRX-480773 can be used for research on AIDS .
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Art. -Nr.: HY-134628S
CAS. Nr.: 1189859-26-4
(Rac)-8,14-Dihydroxy Efavirenz-d4 is the deuterium labeled (Rac)-8,14-Dihydroxy Efavirenz .
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Art. -Nr.: HY-W707595
O-tert-Butyl-2-hydroxy efavirenz-d5 is the deuterium labeled O-tert-Butyl-2-hydroxy Efavirenz (HY-W744274).
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Art. -Nr.: HY-10572BR
CAS. Nr.: 177530-93-7
Synonyms: (Rac)-DMP 266 (Standard); (Rac)-EFV (Standard); (Rac)-L-743726 (Standard)
(Rac)-Efavirenz (Standard) is the analytical standard of (Rac)-Efavirenz. This product is intended for research and analytical applications. (Rac)-Efavirenz is the isomer of Efavirenz (HY-10572). Efavirenz (DMP 266) is a potent inhibitor of the wild-type HIV-1 reverse transcriptase with a Ki of 2.93 nM and exhibits an IC95 of 1.5 nM for the inhibition of HIV-1 replicative spread in cell culture .
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Art. -Nr.: HY-W023836
CAS. Nr.: 154598-53-5
Forschungsgebiete:  

Others

4-Chloro-2-(trifluoroacetyl)aniline (Compound 10), an analog of Efavirenz (HY-10572), is a Pregnane X receptor (PXR) ligand. 4-Chloro-2-(trifluoroacetyl)aniline has no PXR activation activity without induction of Cyp3a11 mRNA expression .
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Art. -Nr.: HY-167690
CAS. Nr.: 1034474-19-5
Target:  

Endogenous Metabolite

Forschungsgebiete:  

Infection

MK-6186 is a novel non-nucleoside reverse transcriptase inhibitor with sub-nanomolar activity against wild-type viruses and the two most common NNRTI-resistant RT mutants (K103N and Y181C). MK-6186 exhibits excellent antiviral activity against K103N and Y181C mutant viruses. When MK-6186 targets 12 common NNRTI-associated mutant viruses, only two relatively rare mutants (Y188L and V106I/Y188L) show high resistance, with FC values exceeding 100, while the FC values of the remaining viruses are all below 10. In addition, when MK-6186 faces 96 clinical virus isolates carrying NNRTI-resistant mutations, most (70%) viruses show more than 10-fold resistance to efavirenz (EFV), while only 29% of mutant viruses show more than 10-fold resistance to MK-6186 .
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Art. -Nr.: HY-E72095
Target:  

Cytochrome P450

Forschungsgebiete:  

Others

Human CYP2A6, Reductase+b5 refers to a near-physiological recombinant microsomal system co-expressed in insect cells, which consists of human cytochrome P450 2A6, NADPH-P450 oxidoreductase (CPR) and cytochrome b5. Human CYP2A6 is a human cytochrome P450 subtype belonging to the CYP2 family, as well as a major metabolic enzyme. It is predominantly expressed in human liver and metabolizes a variety of active compounds including Coumarin (HY-N0709) and nicotine .
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