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HIV

Chemical Structure Cat. No. Product Name CAS No.
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.
Fostemsavir Tris Chemical Structure
 BCP33672 Fostemsavir Tris 864953-39-9
Fostemsavir Tris is an HIV-1 attachment inhibitor in development for the treatment of HIV-1 infection.
PF-3450074 Chemical Structure
 BCP25843 PF-3450074 1352879-65-2
PF-3450074, also known as PF74, is a HIV-1 inhibitor that targets HIV capsid protein. PF74 binds specifically to HIV-1 particles and triggers premature HIV-1 uncoating in target cells.
BID Chemical Structure
 BCP26025 BID 1416258-16-6
BI-D is a novel potent allosteric integrase inhibitor (allini), inhibiting hiv replication
BI-224436 Chemical Structure
 BCP26024 BI-224436 1155419-89-8
BI 224436 is a novel HIV-1 noncatalytic site integrase inhibitor with EC50 values of less than 15 nM against different HIV-1 laboratory strains.
Megestrol acetate Chemical Structure
 BCP29265 Megestrol acetate 595-33-5
Megestrol Acetate is a synthetic progesteronal agent with an IC50 of 260 μM for the inhibition of HegG2.
Indinavir Chemical Structure
 BCP05711 Indinavir 150378-17-9
Indinavir(MK-639; L735524) is a potent and specific HIV protease inhibitor that appears to have good oral bioavailability.
Chloroquine diphosphate Chemical Structure
 BCP31956 Chloroquine diphosphate 50-63-5
Chloroquine diphosphate is an inhibitor of autophagy and toll-like receptors (TLRs). Chloroquine diphosphate is an antimalarial and anti-inflammatory drug widely used to treat malaria and rheumatoid arthritis.
Methyl leucylleucinate hydrochloride Chemical Structure
 BCP31707 Methyl leucylleucinate hydrochloride 6491-83-4
L-Leucyl-L-Leucine methyl ester (LLME) is a lysosomal condensation product that has been reported to be cytotoxic towards natural killer cells and CD4 It has also been shown to induce death of monocytes, polymorphonuclear leukocytes, and myeloid tumor cells.
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