HIV
Human immunodeficiency virus
HIV Isoform Specific Products
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HIV Inhibitors
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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
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(±)-PM 92131
0 ImagesCat. No.: HY-177437CAS No.: 124070-99-1 -
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DC20
0 ImagesCat. No.: HY-176169CAS No.: 2892399-89-0DC20 is an orally active non-nucleoside reverse transcriptase inhibitor with an EC50 of 0.004 μM aganist HIV-1IIIB. -
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18BIOder
0 ImagesCat. No.: HY-117194CAS No.: 275374-93-1 -
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Trovirdine hydrochloride
0 ImagesCat. No.: HY-15350CAS No.: 148311-89-1Synonyms: LY 300046 hydrochlorideTrovirdine hydrochloride (LY300046 hydrochloride) is a selective non-nucleoside HIV-1 reverse transcriptase inhibitor, with an IC50 value of 0.012 μM against the wild-type enzyme. Trovirdine hydrochloride inhibits the replication of both wild-type and mutant HIV-1, and exerts synergistic or additive effects when combined with some antiviral drugs. Trovirdine hydrochloride is applicable to research related to HIV-1 infection. -
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- Vpr (1-14)
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F9170
0 ImagesCat. No.: HY-P10310CAS No.: 2305092-66-2 -
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PROTAC CDK9 degrader-12
0 ImagesCat. No.: HY-181231CAS No.: 3052648-82-2PROTAC CDK9 degrader-12 is a selective CDK9 PROTAC degrader with a DC50 of 23 nM. PROTAC CDK9 degrader-12 induces proteasome-dependent degradation of CDK9, blocks CDK9-mediated HIV-1 transcriptional elongation, and reduces HIV-1 RNA synthesis. PROTAC CDK9 degrader-12 is applicable to research related to HIV-1 infection. -
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Dapivirine-d4
0 ImagesCat. No.: HY-14266S1CAS No.: 1309283-15-5Synonyms: TMC120-d4; R147681-d4Dapivirine-d4 (TMC120-d4) is deuterium labeled Dapivirine. Dapivirine (TMC120), the prototype of diarylpyrimidines (DAPY), is an orally active and nonnucleoside reverse transcriptase inhibitor (NRTI). Dapivirine (TMC120) binds directly to HIV-1 reverse transcriptase. Dapivirine (TMC120) regulates autophagy and induced Akt, Bad and SAPK/JNK activations. -
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Tenofovir alafenamide-d5 fumarate
0 ImagesCat. No.: HY-W653961Synonyms: GS-7340-d5 fumarateTenofovir alafenamide-d5 fumarate (GS-7340-d5 fumarate) is the deuterium labeled Tenofovir alafenamide fumarate (HY-15232A). Tenofovir alafenamide fumarate (GS-7340 fumarate) is an investigational oral proagent of Tenofovir. Tenofovir is a HIV-1 nucleotide reverse transcriptase inhibitor. -
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AGS-009
0 ImagesCat. No.: HY-P991655AGS-009 is a humanized monoclonal neutralising antibody targeting IFN-α. AGS-009 significantly reduces activated lymphocytes, such as CD4+ and CD8+ T cells as well as B cells in SIV infection rhesus macaque models. AGS-009 can be used for autoimmune diseases like systemic lupus erythematosus (SLE) and HIV infections research. -
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VIP (1-12), human, porcine, rat, ovine
0 ImagesCat. No.: HY-P4015CAS No.: 120928-03-2VIP (1-12), human, porcine, rat, ovine is a vasoactive intestinal peptide (VIP) fragment. VIP (1-12), human, porcine, rat, ovine is a ligand for the CD4 (T4)/human immunodeficiency virus receptor. -
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HIV-1 inhibitor-41
0 ImagesCat. No.: HY-147841CAS No.: 3033425-97-4 -
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Ingenol 20-palmitate
0 ImagesCat. No.: HY-137037CAS No.: 39071-33-5Ingenol 20-palmitate (compound 2) is a diterpene that can be found in Euphorbia lath yris. -
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RDEA 806
0 ImagesCat. No.: HY-105249CAS No.: 878670-61-2RDEA 806 is an orally effective non-nucleoside reverse transcriptase (NNRT) inhibitor that exhibits potent in vitro inhibitory activity against wild-type HIV-1 (EC50 = 1.7 ng/mL) and NNRTI-resistant HIV-1. RDEA 806 rapidly reduces HIV-1 RNA viral load in vivo. RDEA 806 has a favorable biosafety profile. RDEA 806 can be used for research related to HIV-1 infection. -
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UC-781
0 ImagesCat. No.: HY-15351CAS No.: 178870-32-1Synonyms: NSC 675186UC-781 (NSC 675186) is a highly potent and selective nonnucleoside reverse transcriptase inhibitor (NNRTI) of HIV-1 with an IC50 value of 5 nM. UC-781 is stable under low PH or various temperatures conditions. UC-781 has antiviral activity and resistance. -
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- HIV-1 capsid inhibitor 1
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APA-H-MPO hydrochloride
0 ImagesCat. No.: HY-115829CAS No.: 1610362-93-0APA-H-MPO hydrochloride is an inhibitor of PCAF bromodomain/Tat-AcK50 interaction with potential for anti-HIV/AIDS. APA-H-MPO hydrochloride can effectively inhibit the binding of PCAF bromodomain to Tat-AcK50. APA-H-MPO hydrochloride showed low cytotoxicity in preliminary cell studies. APA-H-MPO hydrochloride is considered a potential candidate for a promising inhibitory strategy targeting the host cell protein PCAF BRD to block HIV replication. -
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HIV-1 inhibitor-80
0 ImagesCat. No.: HY-172093HIV-1 inhibitor-80 (compound M44) is an HIV-1 inhibitor with an EC50 of 5-148 nM. HIV-1 inhibitor-80 shows good metabolic stability and cytotoxicity in human plasma and human liver microsomes. -
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L-2'-Fd4C
0 ImagesCat. No.: HY-148171CAS No.: 221662-50-6 -
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Withacoagin
0 ImagesCat. No.: HY-N15635CAS No.: 119539-81-0Synonyms: (+)-WithacoaginWithacoagin is a withanolide that can be isolated from the roots of Withania coagulans. Withacoagin has various biological activites such as adaptogenic, anti-inflammatory, and antioxidant properties. Withacoagin regulates the activity of various enzymes and pathways related to oxidative stress and inflammation. Withacoagin can attenuates HIV-1 infection. -
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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.