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
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Fosdevirine
0 ImagesCat. No.: HY-14891CAS No.: 1018450-26-4Synonyms: GSK2248761; FDVFosdevirine (GSK2248761) is is a potent, selective, non-nucleoside reverse transcriptase inhibitor (NNRTI) of human immunodeficiency virus type 1 (HIV-1) replication with low nanomolar activity in vitro. Fosdevirine shows good activity against a broad range of HIV-1 strains, including efavirenz (HY-10572)-resistant clinical isolates. -
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- BNM-III-170
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Trovirdine
0 ImagesSynonyms: LY300046Trovirdine (LY300046) is a selective non-nucleoside HIV-1 reverse transcriptase inhibitor, with an IC50 value of 0.012 μM against the wild-type enzyme. Trovirdine inhibits the replication of both wild-type and mutant HIV-1, and exerts synergistic or additive effects when combined with some antiviral drugs. Trovirdine is applicable to research related to HIV-1 infection. -
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GSK-364735
0 ImagesCat. No.: HY-16907CAS No.: 863434-13-3Synonyms: S/GSK-364735 -
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HIV-1 integrase inhibitor 4
0 ImagesCat. No.: HY-108820CAS No.: 1638504-66-1 -
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HIV-1 integrase inhibitor 3
0 ImagesCat. No.: HY-108817CAS No.: 1638504-56-9 -
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- FGF22-IN-1
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Apelin-36(human) TFA
0 ImagesCat. No.: HY-P1064APurity: 99.42%Apelin-36(human) TFA is an endogenous orphan G protein-coupled receptor APJ agonist, with an EC50 of 20 nM. Apelin-36(human) TFA shows high affinity to human APJ receptors expressed in HEK 293 cells (pIC550=8.61). Apelin-36(human) TFA has been linked to two major types of biological activities: cardiovascular and metabolic. Apelin-36(human) TFA inhibits the entry of some HIV-1 and HIV-2 into the NP2/CD4 cells expressing APJ. -
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(1R)-Tenofovir amibufenamide
0 ImagesSynonyms: (1R)-HS-10234(1R)-Tenofovir amibufenamide ((1R)-HS-10234) is the isomer of Tenofovir amibufenamide, is an orally active antiviral agent. (1R)-Tenofovir amibufenamide ((1R)-HS-10234) is a HIV infection inhibitor and HBV infection inhibitor. (1R)-Tenofovir amibufenamide ((1R)-HS-10234) can be used for HIV infections, hepatitis B research. -
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Bromhexine-d3 hydrochloride
0 ImagesCat. No.: HY-B0372ASPurity: 99.0%Bromhexine-d3 (hydrochloride) is deuterium labeled Bromhexine (hydrochloride). Bromhexine hydrochloride is a potent and specific TMPRSS2 protease inhibitor with an IC50 of 0.75 μM. Bromhexine hydrochloride can prevent and manage SARS-CoV-2 infection. Bromhexine hydrochloride is an autophagy agonist. Bromhexine hydrochloride is a mucolytic cough suppressant and has the potential for a range of respiratory conditions. -
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Emivirine
0 ImagesSynonyms: MKC-442Emivirine (MKC-442) is a non-nucleoside reverse transcriptase inhibitors (NNRTIs) with Ki values of 0.20 and 0.01 μM for dTTP- and dGTP-dependent DNA or RNA polymerase activity, respectively. Emivirine displays potent and selective anti-human immunodeficiency virus type 1 (HIV-1) activity. -
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AZT triphosphate
0 ImagesCat. No.: HY-116364CAS No.: 92586-35-1Synonyms: 3'-Azido-3'-deoxythymidine-5'-triphosphateAZT triphosphate (3'-Azido-3'-deoxythymidine-5'-triphosphate) is a active triphosphate metabolite of Zidovudine (AZT). AZT triphosphate exhibits antiretroviral activity and inhibits replication of HIV. AZT triphosphate also inhibits the DNA polymerase of HBV. AZT triphosphate activates the mitochondria-mediated apoptosis pathway. -
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MK-2048
0 ImagesCat. No.: HY-13305CAS No.: 869901-69-9MK-2048 is a HIV-1 and HIV-1 integrase inhibitor. MK-2048 shows selective activity against HTLV-1-infected cells and retained potency against HIV-1 variants. MK-2048 induces apoptosis, inhibits cell growth, reduces proviral loads, and blocks HTLV-1 transmission and immortalization. MK-2048 can be used for the research of HIV-1 infection. -
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Emtricitabine S-oxide
0 ImagesCat. No.: HY-100096CAS No.: 152128-77-3Synonyms: Emtricitabine sulfoxide; Emtricitabine Degradant-IIIEmtricitabine S-oxide (Emtricitabine sulfoxide) is a major degradation product of Emtricitabine. Emtricitabine is a potent nucleoside reverse transcriptase inhibitor used for the treatment of HIV infection. -
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CK-548
0 ImagesCat. No.: HY-123312CAS No.: 388604-55-5Synonyms: CK-0993548 -
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AZT triphosphate TEA
0 ImagesCat. No.: HY-116364ASynonyms: 3'-Azido-3'-deoxythymidine-5'-triphosphate TEAAZT triphosphate (3'-Azido-3'-deoxythymidine-5'-triphosphate) TEA is a active triphosphate metabolite of Zidovudine (AZT). AZT triphosphate TEA exhibits antiretroviral activity and inhibits replication of HIV. AZT triphosphate TEA also inhibits the DNA polymerase of HBV. AZT triphosphate TEA activates the mitochondria-mediated apoptosis pathway. -
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Cleomiscosin B
0 ImagesCleomiscosin B, a coumarinolignoid, is could isloted from the seeds of Hyoscyamus niger. Cleomiscosin B has potent liver protective. -
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13-Oxyingenol-13-dodecanoate
0 ImagesCat. No.: HY-N0867CAS No.: 54706-70-613-Oxyingenol-dodecanoate (13OD) is a tumor suppressor agent. 13-Oxyingenol-dodecanoate has anti-HIV-1 activity with EC50 value of 33.7 nM.13-Oxyingenol-dodecanoate can induce the expression of ULK1 to effect mitochondrial dysfunction and cellular autophagy. 13-Oxyingenol-dodecanoate also increases the expression of BAX and suppresses the expression of BCL-2 to effect apoptosis. -
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Cabotegravir-d5
0 ImagesSynonyms: GSK-1265744-d5; S/GSK1265744-d5Cabotegravir-d5 is deuterium labeled Cabotegravir. -
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HIV-1 inhibitor-48
0 ImagesHIV-1 inhibitor-48 (compound 13o) is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) and exhibits anti-HIV-1 activity. -
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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.