- Signaling Pathways
- Anti-infection Metabolic Enzyme/Protease
- HIV Protease
HIV Protease
HIV protease, a homodimeric aspartyl protease, is crucial for the viral life-cycle, cleaving proviral polyproteins, hence creating mature protein components that are required for the formation of an infectious virus. HIV protease cleaves newly synthesized polyproteins at the appropriate places to create the mature protein components of an infectious HIV virion. HIV protease is a critical drug target in designing anti-retroviral drugs to treat HIV/AIDS (acquired immune deficiency syndrome).
HIV-1 protease permits viral maturation by processing the Gag and Gag-Pro-Pol polyproteins. It recognizes and cleaves more than 12 different substrates leading to viral maturation. Similar to that of HIV-1, HIV-2 protease is also a homodimeric aspartyl enzyme that plays a vital role in the HIV life-cycle through processing of Gag and Gag-Pro-Pol precursor polyproteins leading to viral maturation.
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HIV Protease Related Products (203)
Related Products (203)
- 20(21)-Dehydrolucidenic acid A
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U-85548E
0 ImagesCat. No.: HY-P2138CAS No.: 124020-62-8U-85548E is an HIV protease inhibitor with nanomolar affinity for HIV-1 aspartic protease. By studying its structure-activity relationship, a potent nanomolar inhibitor with inhibitory effects on both HIV-1 and HIV-2 proteases was designed, and its binding mode was studied by X-ray crystallography and molecular modeling. -
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Lopinavir (Standard)
0 ImagesSynonyms: ABT-378 (Standard)Lopinavir (Standard) is the analytical standard of Lopinavir. This product is intended for research and analytical applications. Lopinavir (ABT-378) is a highly potent, selective peptidomimetic inhibitor of the HIV-1 protease, with Kis of 1.3 to 3.6 pM for wild-type and mutant HIV protease. Lopinavir acts by arresting maturation of HIV-1 thereby blocking its infectivity. Lopinavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 14.2 μM. -
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HIV Protease Substrate 1
0 ImagesCat. No.: HY-P2344CAS No.: 223769-59-3HIV Protease Substrate 1, a fiuorogenic HIV protease substrate, can be used to study enzymatic activity of HIV protease. -
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- HIV-1 protease-IN-13
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JE-2178
0 ImagesCat. No.: HY-123608CAS No.: 210181-19-4 -
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Ganosinensic acid C
0 ImagesCat. No.: HY-N8230CAS No.: 2231756-23-1Ganosinensic acid C is a triterpenoid compound that can be extracted from Ganoderma lucidum. Ganosinensic acid C has important biological activities such as anti-tumor, anti-prostate cancer, anti-inflammatory, and inhibition of HIV-I protease. Ganosinensic acid C has an IC50 value of 10.5 μM against human highly metastatic lung cancer cell line 95D. Ganosinensic acid C has an IC50 value of Ganosinensic acid C against cervical cancer cell line Hela is 13.2 μM. -
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- HIV-1-IN-91
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HIV Protease Substrate I
0 ImagesCat. No.: HY-P3934CAS No.: 124077-63-0HIV Protease Substrate I is a chromogenic substrate of HIV-1 protease. HIV Protease Substrate I has the cleavage site of HIV protease. -
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HIV-1 protease-IN-7
0 ImagesCat. No.: HY-151250CAS No.: 2916441-36-4 -
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Kynostatin 272
0 ImagesCat. No.: HY-106920CAS No.: 147318-81-8Synonyms: KNI 272; Kynostatin; NSC 651714Kynostatin 272 (KNI 272) is a potent HIV protease inhibitor. Kynostatin 272 inhibits the activity of the HIV protease by simulating the substrate transition state of the HIV protease, thus preventing a key step in the replication of the HIV virus. Kynostatin 272 provides an important research foundation for the development of drugs for HIV and AIDS. -
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Agaritine
0 ImagesAgaritine is a compound isolated from the commonly cultivated commercial mushroom Agaricus bisporus. Agaritine is hydrolyzed by an enzyme system present in the mushroom into 4-(hydroxymethyl)benzenediazonium ion, which is a carcinogen in mice. Agaritine is structurally similar to some known carcinogens and can be used for research in cancer and food safety. -
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Stercobilin hydrochloride (mixture of isomers)
0 ImagesCat. No.: HY-159669CAS No.: 13129-80-1Stercobilin hydrochloride (amixture of isomers) is a bile pigment metabolized by gut bacteria, and it's also an HIV protease inhibitor, with a Ki of 4 μM. Stercobilin hydrochloride (a mixture of isomers) can induce pro-inflammatory activity in mouse macrophage RAW264 cells, including the production of TNF-α and IL-1β. Stercobilin hydrochloride (a mixture of isomers) can be used in studies of inflammation and viral infections. -
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- HIV-1 protease-IN-6
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HIV Protease Substrate 1 TFA
0 ImagesCat. No.: HY-P2344AHIV Protease Substrate 1 TFA, a fiuorogenic HIV protease substrate, can be used to study enzymatic activity of HIV protease. -
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GS-9770
0 ImagesCat. No.: HY-162525CAS No.: 2306328-43-6GS-9770 is an orally active inhibitor for HIV protease with Ki of 0.16 nM. GS-9770 exhibits antiviral activity aginst HIV-1 strains and HIV-2 strains with EC50 of 1.9-26 nM, and 26 nM. GS-9770 is metabolic stable in human liver microsomes. GS-9770 exhibits good pharmacokinetic characters in Sprague Dawley rats. -
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L 756423
0 ImagesCat. No.: HY-106188CAS No.: 216863-66-0 -
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- R-87366
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- U-89360E
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- HIV-1-IN-84
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