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HIV

Chemical Structure Cat. No. Product Name CAS No.
Hexamethyleneamiloride Chemical Structure
BCP41883 Hexamethyleneamiloride 1428-95-1
Hexamethyleneamiloride is a member of the class of pyrazines that is amiloride in which the two amino hydrogens at position N-5 are replaced by a hexamethylene moiety, resulting in the formation of an azepane ring. It has a role as a sodium channel blocker, an apoptosis inducer, an antineoplastic agent and an odorant receptor antagonist.
IMB-301 Chemical Structure
BCP40899 IMB-301 64009-84-3
IMB-301 is a small molecule inhibitor that target the binding interface of the HIV-1 Vif/hA3G complex, inhibits the replication of HIV-1 in H9 cells (IC50=8.63 uM).
Lenacapavir Chemical Structure
BCP40764 Lenacapavir 2189684-44-2
Lenacapavir, also known as GS-6207, is a HIV-1 capsid inhibitor.
Islatravir Chemical Structure
BCP38832 Islatravir 865363-93-5
Islatravir is a potential antiviral drug for the treatment of HIV infection.
PNU-103017 Chemical Structure
BCP36734 PNU-103017 166335-18-8
PNU-103017 is an HIV protease inhibitor.
Methyl gallate Chemical Structure
BCP36294 Methyl gallate 99-24-1
Methyl gallate is a plant phenolic with antioxidant, anticancer, and anti-inflammatory activities. Methyl gallate also shows bacterial inhibition activity. Methyl gallate also has anti-HIV-1 and HIV-1 enzyme inhibitory activities.
MK-0536 Chemical Structure
BCP35146 MK-0536 865298-83-5
MK‐0536 is a potent HIV-1 integrase strand transfer inhibitor.
BRD-K98645985 Chemical Structure
BCP34714 BRD-K98645985 1357647-78-9
BRD-K98645985 is an inhibitor of BAF transcriptional repression which targets specific ARID1A-containing BAF complexes, and reverses HIV-1 latency, and is non-toxic to T cells.
JE-2147 Chemical Structure
BCP34046 JE-2147 186538-00-1
JE-2147 is a dipeptide HIV protease inhibitor (PI) that is effective against a wide spectrum of HIV-1, HIV-2, simian immunodeficiency virus, and various clinical HIV-1 strains in vitro.
RN-18 Chemical Structure
BCP33989 RN-18 431980-38-0
RN-18 is a HIV-1 viral infectivity factor (HIV-1 Vif) inhibitor with an IC50 of 6 μM in nonpermissive H9 cells.
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