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HIV

Chemical Structure Cat. No. Product Name CAS No.
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.
Tipranavir Chemical Structure
 BCP22007 Tipranavir 174484-41-4
Tipranavir is an HIV-1 protease inhibitor. It has a role as a HIV protease inhibitor and an antiviral drug.
Isoprinosine Chemical Structure
 BCP21366 Isoprinosine 36703-88-5
Inosine pranobex is a potent, broad-spectrum antiviral compound for HIV infection. Inosine pranobex is an immunopotentiator.
Nelfinavir mesylate Chemical Structure
 BCP21142 Nelfinavir mesylate 159989-65-8
Nelfinavir Mesylate is the mesylate salt form of nelfinavir, a synthetic antiviral agent that selectively binds to and inhibits human immunodeficiency virus (HIV) protease. Nelfinavir has activity against HIV 1 and 2.
4-Hydroxycoumarin Chemical Structure
 BCP31120 4-Hydroxycoumarin 1076-38-6
4-Hydroxycoumarin is a plant derived antioxidant, protecting against lipid peroxidation, as well as a potential inhibitor of HIV-1 Integrase.
Oleanonic acid Chemical Structure
 BCP15429 Oleanonic acid 17990-42-0
Oleanolic acid is a natural compound isolated from the leaves of Eriobotrya japonica Thunb.
Gardiquimod TFA Chemical Structure
 BCP30186 Gardiquimod TFA 1159840-61-5
Gardiquimod trifluoroacetate is a specific TLR7 agonist which can also inhibit HIV-1 reverse transcriptase.
Gardiquimod Chemical Structure
 BCP30187 Gardiquimod 1020412-43-4
Gardiquimod is a chemical compound which acts selectively at both mouse and human forms of toll-like receptor 7 (TLR7). It functions as an immune response modifier.
DL-Thioctic acid Chemical Structure
 BCP13221 DL-Thioctic acid 1077-28-7
Alpha-Lipoic Acid is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. α-Lipoic Acid inhibits NF-κB-dependent HIV-1 LTR activation.
Nevirapine Chemical Structure
 BCP05587 Nevirapine 129618-40-2
Nevirapine is a non-nucleoside inhibitor of HIV-1 reverse transcriptase used to treat and prevent HIV/AIDS; with a Ki of 270 μM.
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