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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| A052 | Nirsevimab Biosimilar (Anti-RSV Reference Antibody) Featured |
Nirsevimab (MEDI8897) is a recombinant monoclonal antibody against human respiratory syncytial virus (RSV). Nirsevimab has neutralizing activity against RSV A and RSV B viruses, with IC50 values of 5.42 ng/mL and 9.71 ng/mL, respectively. Nirsevimab can be used for research on respiratory infections.
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| A054 | Raxibacumab Biosimilar(Anti-PA Reference Antibody) Featured |
Raxibacumab (ABthrax) is a human IgG1 monoclonal antibody against Bacillus anthracis protective antigen (PA). Raxibacumab blocks the toxin’s deleterious effects by preventing binding of the protective antigen component of the anthrax toxin to its receptors in host cells, thereby blocking the toxin’s deleterious effects. Raxibacumab can be used for anti-anthrax research.
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| DC66561 | Peracetylated GalNAc succinimidyl pentanoate Featured |
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| DC66572 | Peracetylated GalNAc PEG linker-Amino-2 Featured |
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| DC66568 | Peracetylated GalNAc PEG linker-Amino-1 Featured |
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| DC66564 | Peracetylated GalNAc PEG linker-Acid-1 Featured |
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| DC66575 | Peracetylated GalNAc PEG linker-Acid-2 Featured |
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| DC66551 | GalNAc-Cluster-HHA-CE Phosphoramidite Featured |
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| DC66565 | Peracetylated GalNAc-L96-Acid-1 Featured |
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| DC66559 | Peracetylated GalNAc PEG linker-Azide Featured |
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| DC65562 | GalNAc-NAG-25 Phosphoramidite Featured |
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| DC66549 | GalNAc-NAG-37 Phosphoramidite Featured |
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| DC47877 | tri-GalNAc-COOH (acetylation) Featured |
tri-GalNAc-COOH acetylation is the acetylated and modified form of tri-GalNAc-COOH. tri-GalNAc-COOH acetylation can be used for the synthesis of LYTAC.
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| DC66574 | Peracetylated GalNAc-L96-1 Featured |
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| DC66557 | GalNAc-L96 Linker-Azide Featured |
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| DC65559 | GalNAc-L96 Phosphoramidite Featured |
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| DC66555 | GalNAc-L96 Linker-Acid Featured |
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| DC33111 | Tesofensine(NS-2330) Featured |
Tesofensine (NS-2330) is a triple monoamine reuptake inhibitor inducing a potent inhibition of the re-uptake process in the synaptic cleft of the neurotransmitters dopamine (DA; IC50=6.5 nM), norepinephrine (NE;IC50=1.7 nM), and serotonin (5-HT;IC50=11 nM), and with potentials as an anti-obesity agent. Tesofensine is a CNS acting anti-obesity agent.
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| DC65560 | GalNAc-L96 free base Featured |
GalNAc-L96 free base, the G-rich oligonucleotides carrying the longer GalNAc linker that can be used for delivery of nucleic acid drugs.
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| DC66550 | GalNAc-Cluster-COOH Featured |
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| DC72546 | Tri-GalNAc-NHS ester Featured |
Tri-GalNAc-NHS ester is a LYsosome TArgeting Chimera (LYTAC) and a ligand of asialoglycoprotein receptor (ASGPR). ASGPR is a lysosomal targeting receptor specifically expressed on liver cells, for the degradation of extracellular proteins including membrane proteins. Tri-GalNAc-NHS ester can be used as a protein degrader and it can be used for the research of LYTAC.
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| DC66569 | GalNAc-L96-Amide Featured |
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| DC66548 | GalNAc-Lipid GL3 Featured |
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| DC65965 | Tri-GalNAc(OAc)3 Featured |
Tri-GalNAc(OAc)3 is a triantenerrary N-acetylgalactosamine (tri-GalNAc) with an amino group, which is useful precursor for synthesis of GalNAc-LYTAC that engage the asialoglycoprotein receptor for targeted protein degradation. Tri-GalNAc(OAc)3 was first reported in Nat Chem Biol. 2021 Sep;17(9):937-946 (compound ). This product has no formal name at the moment.
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| DC46965 | Tri-GalNAc-COOH Featured |
tri-GalNAc-COOH is an asialoglycoprotein receptor (ASGPR) ligand that can be used for LYsosome TArgeting Chimera (LYTAC) research.
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| DC65564 | GalNAc-L96-PS Featured |
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| DC65563 | GalNAc-L96-CPG Featured |
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| DC71975 | TriGalNAc CBz Featured |
TriGalNAc CBz is a GalNAc derivative and tri-GalNAc is an asialoglycoprotein receptor (ASGPR) ligand. TriGalNAc CBz can be used for mRNA drug delivery as well as lysosomal targeted chimerism (LYTAC) studies.
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| DC60771 | (+/-)-AC 7954 Hydrochloride Featured |
AC-7954 is a selective nonpeptidic urotensin receptor agonist (EC50: 300 nM at the human UII receptor).
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| DC60770 | PKCTheta-IN-2 Featured |
PKCTheta-IN-2 (compound 14) is a potent and selective PKCθ inhibitor with an IC50 of 0.25 nM. PKCTheta-IN-2 shows good selectivity over a wide range of kinases, including the PKC subfamily (30 kinases). PKCTheta-IN-2 inhibits the IL-2 production in a mouse (IC50 of 682 nM).
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