HIV
Human immunodeficiency virus
HIV Isoform Specific Products
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HIV Inhibitors
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HIV Antagonists
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HIV Activators
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HIV Modulator
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HIV Inducers
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HIV Degrader
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HIV Controls
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HIV Ligand
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HIV Proteins
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HIV Related Products (1395)
Related Products (1395)
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Recombinant Proteins (27)
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Antibodies (6)
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HIV Isoform Comparison
- HIV-1 inhibitor-44
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- HIV-1 Nef-IN-1
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α-Lipoic Acid sodium (Standard)
0 ImagesSynonyms: Thioctic acid sodium (Standard); (±)-α-Lipoic acid sodium (Standard); DL-α-Lipoic acid sodium (Standard)α-Lipoic Acid (sodium) (Standard) is the analytical standard of α-Lipoic Acid (sodium). This product is intended for research and analytical applications. α-Lipoic Acid (Thioctic acid) sodium is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. α-Lipoic Acid sodium inhibits NF-κB-dependent HIV-1 LTR activation. α-Lipoic Acid sodium induces endoplasmic reticulum (ER) stress-mediated apoptosis in hepatoma cells. α-Lipoic Acid sodium can be used with CPUL1 (HY-151802) to construct the self-assembled nanoaggregate CPUL1-LA NA, which has improved antitumor efficacy than CPUL1. -
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- HIV-1 integrase inhibitor 9
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BEA 005
0 ImagesCat. No.: HY-105394CAS No.: 132235-73-5BEA 005 is an antivirus agent. BEA 005 can block early systemic and mucosal infections with SIV and HIV-2. -
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Fleephilone
0 ImagesCat. No.: HY-N14366CAS No.: 183239-76-1 -
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- HIV-1 inhibitor-36
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DPP9-IN-2
0 ImagesCat. No.: HY-179348CAS No.: 3020859-44-0DPP9-IN-2 is a selective, potent and orally active inhibitor of Dipeptidyl Peptidase 9 (DPP9 ) with an IC50 of 12.9 nM. DPP9-IN-2 shows a SI of 59 over DPP8, and shows no significant inhibitory activity against related peptidases including DPP2, DPP4, FAP, and PREP. DPP9-IN-2 can induce cancer cells pyroptosis and has weak synergistic anti-HIV-1 activity when combined with non-nucleoside reverse transcriptase inhibitor. DPP9-IN-2 can be used for the researches of cance rand infection. -
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- Antitumor agent-191
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- Antiviral agent 29
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HI-236
0 ImagesCat. No.: HY-121611CAS No.: 233271-65-3 -
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F1839-I
0 ImagesCat. No.: HY-N11430CAS No.: 159096-49-8F1839-I is a compound that can be isolated from Stachybotrys. F1839-I has weak cytotoxicity and anti-HIV activity with an IC50 value of 15.6 μM. -
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Soulattrolide
0 ImagesCat. No.: HY-182552CAS No.: 65025-62-9Soulattrolide is a non-nucleoside HIV-1 reverse transcriptase (RT) inhibitor with IC50 values of 0.34 µM for HIV-1 RT, 69.5 µM for E. coli RNase H, and >495 µM for human DNA polymerase β, and can be found in Calophyllum teysmannii latex. Soulattrolide can be used for the research of HIV-1 infection, pain, inflammation, and Mycobacterium tuberculosis infection. -
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Maraviroc (Standard)
0 ImagesSynonyms: UK-427857 (Standard)Maraviroc (Standard) is the analytical standard of Maraviroc. This product is intended for research and analytical applications. Maraviroc (UK-427857) is a selective CCR5 antagonist with activity against human HIV. -
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NSC 13987
0 ImagesNSC 13987 is a Nef site I inhibitor. NSC 13987 binds to Nef site I and disrupts the Nef-calnexin interaction. NSC 13987 restores cholesterol efflux inhibited by Nef. NSC 13987 is applicable to the research of HIV-associated atherosclerosis. -
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VIRIP
0 ImagesCat. No.: HY-P10437CAS No.: 339332-64-8Synonyms: human α1-AT(353-372) -
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HIV-1 tat Protein (1-9)
0 ImagesCat. No.: HY-P11152CAS No.: 200203-20-9HIV-1 tat Protein (1-9) occurs extracellularly and has a role in the immunosuppression of non-HIV-1-infected T cells in acquired AIDS. HIV-1 tat Protein (1-9) is an inhibitor of DP IV. HIV-1 tat Protein (1-9) can be synthesized by phase peptide synthesis with Fmoc (N-(9-fluorenyl)methoxycarbonyl) technique using the peptide synthesizer 431A. HIV-1 tat Protein (1-9) can be studied in research on HIV-1. -
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Kadsuracoccinic acid A
0 ImagesCat. No.: HY-113818CAS No.: 1016260-22-2Kadsuracoccinic acid A is a tetracyclic natural compound that can be isolated from the stems of Kadsura coccinea. Kadsuracoccinic acid A has vitro anti-HIV-1 activitiy with an EC50 value of 68.7 μM. -
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Ancriviroc
0 ImagesCat. No.: HY-107401CAS No.: 370893-06-4Synonyms: SCH-351125Ancriviroc (SCH-351125) is an orally active CCR5 antagonist with an IC50 value of 13 nM against hCCR5. Ancriviroc specifically binds to hCCR5, blocks ligand-induced signal transduction, calcium influx, GTPγS binding, chemotaxis, ligand binding, and HIV-1 entry, induces conformational changes in CCR5, and inhibits infection and replication of R5-tropic HIV-1. -
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CXCR4 antagonist 7
0 ImagesCat. No.: HY-147808CAS No.: 1185451-72-2CXCR4 antagonist 7 (Compound PARA-B) is a CXCR4 antagonist with the IC50 of 9.3 nM. CXCR4 antagonist 7 can be used for the research of HIV infection, inflammatory diseases, cancer, and WHIM syndrome. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.