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 (1381)
Related Products (1381)
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Recombinant Proteins (26)
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Antibodies (6)
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HIV Isoform Comparison
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ddATP lithium
0 ImagesCat. No.: HY-128036DSynonyms: 2',3'-Dideoxyadenosine 5'-triphosphate lithiumddATP (lithium) (2',3'-Dideoxyadenosine 5'-triphosphate (lithium)) is an active metabolite of 2',3'-dideoxyinosine and a DNA polymerase chain elongation inhibitor. ddATP (lithium) is used in Sanger DNA sequencing and in research related to viral infection[1][2][3][4][5]. -
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Saquinavir-13C6
0 ImagesCat. No.: HY-17007S2Synonyms: Ro 31-8959-13C6Saquinavir-13C6 (Ro 31-8959-13C6) is 13C labeled Saquinavir (HY-17007). Saquinavir (Ro 31-8959) is an orally active HIV protease inhibitor that can be used in the research of AIDS. Saquinavir also has anti-inflammatory activity and can induce apoptosis of human red blood cells. -
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- GSK-214096
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HEPT
0 ImagesCat. No.: HY-10892CAS No.: 123027-56-5HEPT is a potent and selective anti-HIV-1 agent. -
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Cobicistat (Standard)
0 ImagesSynonyms: GS-9350 (Standard)Cobicistat (Standard) is the analytical standard of Cobicistat. This product is intended for research and analytical applications. Cobicistat is a potent and selective inhibitor of cytochrome P450 3A (CYP3A) enzymes with IC50s of 30-285 nM. Cobicistat is a pharmacokinetic enhancer which increases the overall absorption of several HIV medications. -
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12-Methoxydodecanoic acid
0 ImagesCat. No.: HY-W787717CAS No.: 92169-28-312-Methoxydodecanoic acid, a heteroatom-containing analog of myristic acid, possesses anti-viral activity against HIV, with an IC50 of 6.8 μM. 12-Methoxydodecanoic acid inhibits moloney murine leukemia virus (MoMLV). -
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HIV-IN-14
0 ImagesCat. No.: HY-184492CAS No.: 3069129-78-5HIV-IN-14 is an agent that binds to the HIV-1 reverse transcriptase p66 domain (monomeric GAG-POL), and also acts as a selective cytotoxic agent. HIV-IN-14 promotes GAG-POL dimerization, which in turn leads to premature activation of intracellular viral protease. HIV-IN-14 selectively kills HIV-infected cells expressing GAG-POL without exerting cytotoxicity on non-HIV-infected cells. HIV-IN-14 can be used in the research of HIV infection, acquired immunodeficiency syndrome (AIDS) or AIDS-related complex (ARC). -
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Rilpivirine (Standard)
0 ImagesSynonyms: R278474 (Standard); TMC278 (Standard); DB08864 (Standard)Rilpivirine (Standard) is the analytical standard of Rilpivirine. This product is intended for research and analytical applications. Rilpivirine (R278474) is a potent and specific diarylpyrimidine (DAPY) non-nucleoside reverse transcriptase inhibitor (NNRTI). Rilpivirine has high antiviral activity against wild-type HIV (EC50=0.4 nM) and mutant viruses (EC50=0.1-2.0 nM). Rilpivirine has a high genetic barrier to resistance development of HIV. -
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GSK163929
0 ImagesCat. No.: HY-12944CAS No.: 716354-04-0GSK163929 (compound 122) is an orally active, anti-HIV CCR5 antagonist with low inhibitory potency against hEGR. GSK163929 had no adverse effects in rats at 2000 mg/kg/day (i.v., 7 d) and in dogs at 250 mg/kg/day (i.v., 7 d). -
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Dexelvucitabine (Standard)
0 ImagesCat. No.: HY-14920RCAS No.: 134379-77-4Synonyms: Reverset (Standard); d-d4FC (Standard)Dexelvucitabine (Standard) is the analytical standard of Dexelvucitabine. This product is intended for research and analytical applications. Dexelvucitabine (Reverset; d-d4FC), a Cytidine (HY-B0158) analog, is an orally active nucleoside reverse transcriptase inhibitor. Dexelvucitabine is a powerful agent against HIV-1-resistant viruses containing a thymidine analog and/or M184V mutation in the viral polymerase. Dexelvucitabine is a 2′-Deoxycytidine antiretroviral agent. -
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rac-TNT-i
0 ImagesCat. No.: HY-157469ASynonyms: rac-NPD3064rac-TNT-i (rac-NPD3064) is the racomer of TNT-i (HY-157469). TNT-i is an inhibitor targeting M-Sec. TNT-i reversibly inhibits the formation of tunnel nanotubes (TNT) induced by M-Sec. TNT-i can reduce the production of wild-type HIV-1 in macrophages and T cells expressing M-Sec. TNT-i has low cytotoxicity towards macrophages and T cells. TNT-i can be used in studies related to HIV-1 infection. -
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- HIV-1 inhibitor-78
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NNRT-IN-15
0 ImagesCat. No.: HY-181034NNRT-IN-15 (Compound 16a) is a potent non-nucleoside reverse transcriptase (NNRT) inhibitor. NNRT-IN-15 shows an EC50 of 3 nM for WT HIV-1 and inhibits seven mutant strains (L100I, K103N, Y181C, etc.) (EC50 = 8.2-43.4 nM). NNRT-IN-15 has low cytotoxicity against MT-4 cells (CC50 = 196.46 μM). NNRT-IN-15 also inhibit WTHIV-1RT and hERG with IC50 values of 0.7599 μM and 27.455 μM. NNRT-IN-15 can be used for research of HIV-1 infection. -
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CT 2576
0 ImagesCat. No.: HY-187609CAS No.: 166981-11-9CT 2576 is a phospholipid signaling inhibitor as well as a Jak3/STAT5 inhibitor. CT 2576 suppresses gene expression and replication of human immunodeficiency virus (HIV) at the post-transcriptional level by interfering with phospholipid metabolism in host cells, particularly by inhibiting the production of phosphatidic acid PA. CT-2576 completely inhibits the growth and proliferation of malignant T-cell lymphoma cells by suppressing phospholipid signaling and blocking the Jak/STAT signaling pathway associated with IL-2R. CT 2576 can be used in research related to human immunodeficiency virus (HIV) infection and cutaneous T-cell lymphoma (CTCL). -
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- 27-Hydroxywithanone
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Sodium diethylcarbamodithioate trihydrate, ACS, 99.0%
0 ImagesCat. No.: HY-W009722ACAS No.: 20624-25-3Synonyms: Ditiocarb sodium trihydrate, ACS, 99.0%Sodium diethylcarbamodithioate trihydrate, ACS, 99.0% (Ditiocarb sodium trihydrate, ACS, 99.0%) is a copper reagent. The reaction with Cu2+ solution resulted in the formation of a complex, which increased the copper displacement precipitation rate. Sodium diethylcarbamodithioate trihydrate, ACS, 99.0% can reduce HIV infection and can be used in adjuvant immune research of high-risk breast cancer. -
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Nonoxynol-9
0 ImagesCat. No.: HY-W587782CAS No.: 14409-72-4 -
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Cholesterol heptanoic acid
0 ImagesCat. No.: HY-17671CAS No.: 103003-24-3Cholesterol heptanoic acid is a lipophilic Cholesterol (HY-N0322) derivative. Cholesterol heptanoic acid can combine with peptides (such as peptides P1 and P2) to form lipopeptides, which possess antiviral activity. Cholesterol heptanoic acid can be used for research of HIV infection. -
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ML416
0 ImagesCat. No.: HY-125613CAS No.: 2043014-84-0ML416 is a broad-spectrum antiviral agent. ML416 inhibits host de novo pyrimidine biosynthesis, and induces a variety of interferon-stimulated genes (ISGs). ML416 can be used for the research of viral infections including alphaviruses, influenza virus, and HIV-1. -
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Plerixafor (Standard)
0 ImagesSynonyms: AMD 3100 (Standard); JM3100 (Standard); SID791 (Standard)Plerixafor (Standard) is the analytical standard of Plerixafor. This product is intended for research and analytical applications. Plerixafor (AMD 3100) is a selective CXCR4 antagonist with an IC50 of 44 nM. Plerixafor, an immunostimulant and a hematopoietic stem cell (HSC) mobilizer, is an allosteric agonist of CXCR7. Plerixafor inhibits HIV-1 and HIV-2 replication with an EC50 of 1-10 nM. -
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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.