Name | 2-(4-(Pyrazin-2-yl)piperazin-1-yl)pyrimidine |
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Synonyms | MFCD06371724 |
Description | HIV-1 inhibitor-47 is an inhibitor of HIV-1, and inhibits vif-dependent degradation of human APOBEC3G, with an IC50 value of 14.33 μM. HIV-1 inhibitor-47 also involves in derivatives of 1-(2-pyrimidinyl)piperazine synthesis, with potential antianxiety, antidepressant, and antipsychotic effect[1][2][3]. |
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Related Catalog | |
Target |
HIV (Vif-dependent degradation of human APOBEC3G)[1] |
In Vitro | APOBEC3G (A3G), a host cytidine deaminase that can block HIV-1 replication and shows antiviral activity. However HIV-1 develops the ability to hijack the cellular ubiquitin/proteasome degradation pathway[1]. HIV-1 inhibitor-47 targets APOBEC3G-apolipoprotein B mRNA editing enzyme catalytic subunit 3G (human), and works on the HIV-1 Vif-APOBEC3G interaction[2]. |
References |
[3]. Pubchem: 2-(4-(Pyrazin-2-yl)piperazin-1-yl)pyrimidine-BioAssay Results. |
Molecular Formula | C12H14N6 |
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Molecular Weight | 242.28 |
Storage condition | 2-8°C |