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-52
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- HIV-1 inhibitor-18
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HIV-1 inhibitor-14
0 ImagesCat. No.: HY-144113CAS No.: 2761172-65-8 -
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gp120-IN-2
0 ImagesCat. No.: HY-144731CAS No.: 123629-42-5gp120-IN-2 (compound 4i) is a potent HIV-1 gp120 inhibitor with an IC50 of 7.5 µM and CC50 of 112.93 µM. gp120-IN-2 shows anti-HIV-1 activity. gp120-IN-2 shows cytotoxicity in a dose dependent manner in SUP-T1 cells. -
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- U-89360E
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HIV-1 inhibitor-23
0 ImagesCat. No.: HY-146018CAS No.: 2554622-28-3 -
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Apelin-17(human, bovine) TFA
0 ImagesCat. No.: HY-P1066AApelin-17(human, bovine) TFA is an endogenous orphan G protein-coupled receptor APJ agonist. Apelin-17(human, bovine) TFA binds to human APJ receptors expressed in HEK 293 cells (pIC50=9.02). Apelin-17(human, bovine) TFA inhibits the entry of some HIV-1 and HIV-2 into the NP2/CD4 cells expressing APJ. -
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Hypocrellin A (Standard)
0 ImagesCat. No.: HY-N2575RCAS No.: 77029-83-5Hypocrellin A (Standard) is the analytical standard of Hypocrellin A. This product is intended for research and analytical applications. Hypocrellin A is a PKC inhibitor that exerts antidiabetic activity by reversing the effects of high glucose on endothelin (ET-1) expression. Hypocrellin A is also a photosensitizer for photodynamic therapy (PDT) with anticancer, antibacterial and antiviral activities, especially against human immunodeficiency virus (HIV). In addition, Hypocrellin-A also possesses anti-Leishmania activity (IC50=0.27 μg/ml)[1][2][3][4][5][6][7][8][9]. -
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- HIV-1-IN-84
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- L 694746
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Ritonavir-13C,d3
0 ImagesCat. No.: HY-90001S1CAS No.: 2937755-89-8Synonyms: ABT 538-13C,d3; RTV-13C,d3 -
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GSK812397
0 ImagesCat. No.: HY-111224CAS No.: 878197-98-9GSK812397 is a CXCR4 antagonist with potential for the treatment of HIV infection. To evaluate the clinical potential of GSK812397, kilogram-scale agent candidates are needed. Here, an improved, scalable synthetic route for the CXCR4 antagonist GSK812397 is described. This new route has been scaled up in a 50-liter stationary facility to obtain 1.2 kg of agent substance in 20% overall yield and >99% chemical and enantiomeric purity in five steps. CXC chemokine receptor 4 (CXCR4) is a 7-transmembrane protein that functions in part as a host co-receptor for multiple strains of HIV-1. It is thought that targeting CXCR4 will help inhibit the replication of several late cytopathic viruses; therefore, CXCR4 antagonists are one of the most promising new classes of experimental anti-HIV agents. GSK812397 is a potent CXCR4 antagonist and is therefore a candidate for investigation for the treatment of HIV infection. -
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- DMJ-I-228
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APA-APA-MPO dihydrochloride
0 ImagesCat. No.: HY-115828CAS No.: 1610362-98-5APA-APA-MPO dihydrochloride is an inhibitor of PCAF bromodomain/Tat-AcK50 interaction with reduced cytotoxic activity. APA-APA-MPO dihydrochloride can effectively inhibit the binding of PCAF to Tat-AcK50, showing its potential in HIV/AIDS inhibitory strategies. APA-APA-MPO dihydrochloride can be used in studies that hinder HIV replication. -
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Dapivirine hydrochloride
0 ImagesCat. No.: HY-14266ACAS No.: 244768-47-6Dapivirine hydrochloride is a non-nucleoside reverse transcriptase inhibitor with antitumor activity. Dapivirine hydrochloride attenuates the proliferation of glioblastoma cells and induces apoptosis. Dapivirine hydrochloride modulates autophagy and activates Akt, Bad, and SAPK/JNK signaling pathways. Dapivirine hydrochloride has shown inhibitory effects on glioma cell growth both in vitro and in vivo. Dapivirine hydrochloride is also a promising drug candidate for topical microbial agents for the prevention of sexual transmission of HIV-1. -
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DMP-851
0 ImagesCat. No.: HY-19281CAS No.: 188978-02-1DMP-851 is a cyclic urea HIV protease inhibitor, with a Ki of 0.021 nM. DMP-851 shows antiviral activity against laboratory strains of HIV-l and HIV-2 as well as against primary clinical isolates derived from Zidovudine (HY-17413)-resistant samples (A018C, E, WR 10983). -
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5M038
0 ImagesCat. No.: HY-122204CAS No.: 338962-32-65M038 is an inhibitor of HIV envelope-mediated fusion with potent inhibitory activity against gp41-mediated membrane fusion. 5M038 prevents the formation of the gp41 post-fusion conformation and inhibits envelope-mediated membrane fusion in cell-cell fusion and viral infectivity assays. 5M038 has shown broad fusion inhibition in tests against multiple HIV-1 subtypes, including M and T strains. 5M038 targets a highly conserved hydrophobic pocket and binds to the gp41 trimer, thereby exerting its inhibitory effect. -
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- HIV-IN-9
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Saquinavir-d9
0 ImagesCat. No.: HY-17007SCAS No.: 1356355-11-7Synonyms: Ro 31-8959-d9Saquinavir-d9 (Ro 31-8959-d9) is the deuterium 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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ZINC36617540
0 ImagesCat. No.: HY-120465CAS No.: 1174905-91-9ZINC36617540 is a novel Nef protein inhibitor with anti-HIV activity. ZINC36617540 exhibits superior binding affinity by binding to Nef protein. ZINC36617540 shows a similar binding mode to the prototype molecule B9 in molecular docking. The mechanism of action of ZINC36617540 mainly depends on its hydrophobic and electrostatic interactions with Nef protein. -
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Your Search Returned No Results.
Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.