Home   >  
Microbiology/Virology
  >  
HIV

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

HIV

Chemical Structure Cat. No. Product Name CAS No.
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.
Lavendustin B Chemical Structure
 BCP20779 Lavendustin B 125697-91-8
Lavendustin B is a Tyrosine Kinase Inhibitor amd an inhibitor of HIV-1 integrase (IN) interaction with its cognate cellular cofactor, lens epithelium-derived growth factor (LEDGF/p75).
AVX754 Chemical Structure
 BCP07907 AVX754 160707-69-7
Apricitabine, also known as (-)-BCH-10652; (-)-dOTC; AVX-754; BCH-10618; SPD-754, is an experimental nucleoside reverse transcriptase inhibitor (NRTI) against HIV.
MK-2048 Chemical Structure
 BCP03947 MK-2048 869901-69-9
MK-2048 is a potent inhibitor of integrase (IN) and INR263K with IC50 of 2.6 nM and 1.5 nM, respectively.
3-Deazaadenosine Chemical Structure
 BCP18416 3-Deazaadenosine 6736-58-9
3-Deazaadenosine is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 µM; has anti-inflammatory, anti-proliferative and anti-HIV activity.
123下一页末页共 75 条记录 1 / 8 页 
0086-15971444841