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HIV

Chemical Structure Cat. No. Product Name CAS No.
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.
KP1461 Chemical Structure
BCP23972 KP1461 943540-08-7
KP-1461 is a deoxycytidine analogue that is randomly inserted into HIV DNA by reverse transcriptase where it can cause base mispairing and introduce mutations that decrease viral fitness.
TAK-779 Chemical Structure
BCP28073 TAK-779 229005-80-5
TAK-779 is a highly potent and selective nonpeptide CCR5 antagonist with a IC50 value of 1.4 nM in the binding assay, TAK-779 also inhibited the replication of macrophage (M)-tropic HIV-1 (Ba-L strain) in both MAGI-CCR5 cells and PBMCs with EC50 values of 1.2 and 3.7 nM, respectively.
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