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Home > RNA Delivery > siRNA/ASOs/Aptamer drugs

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  Cat. No.:  DC67027   Featured
Chemical Structure
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More than 5000 active chemicals with high quality for research!
Field of application
Chemicals PropertiesBiological activity COA & MSDSRelated productsDatasheet
Cas No.:
Purity: >95%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Target: TTR
MSDS
Cat. No. Product name Field of application
DC67234 CPG-1018
DC67028 Pegaptanib
DC67027 Onpattro
DC67025 Mipomersen Mipomersen (ISIS 301012 free base) is an antisense oligonucleotide inhibitor of apolipoprotein B (apoB). Mipomersen has anti-HCV effect and reduces the infectivity of the HCV. Mipomersen can be used for the research of homozygous familial hypercholesterolemia (HoFH). The free form of the compound is prone to instability, it is advisable to consider the stable salt form (Mipomersen sodium) that retains the same biological activity.
DC67024 Inotersen Inotersen is an antisense oligonucleotide that inhibits hepatic production of transthyretin (TTR). The free form of the compound is prone to instability, it is advisable to consider the stable salt form (Inotersen sodium) that retains the same biological activity.
DC67023 Amvuttra
DC72286 Fomivirsen Fomivirsen (ISIS-2922 free base) is an antisense 21 mer phosphorothioate oligonucleotide. Fomivirsen is an antiviral agent that is used cytomegalovirus retinitis (CMV) research, incluiding in AIDs. Fomivirsen binds to and degrades the mRNAs encoding CMV immediate-early 2 protein, thus inhibiting virus proliferation.
DC47310 Rovanersen Rovanersen (WVE-120101) is an antisense oligonucleotide that can be used for huntington’s disease research.
DC47308 Lumasiran Lumasiran (ALN-G01), a siRNA product, reduces hepatic oxalate production by targeting glycolate oxidase. By silencing the gene encoding glycolate oxidase, Lumasiran depletes glycolate oxidase and thereby inhibits the synthesis of oxalate, which is the toxic metabolite that is directly associated with the clinical manifestations of Primary hyperoxaluria type 1 (PH1).
DC47306 ARO-AAT ARO-AAT is a second-generation RNAi drug. ARO-AAT consistes of a cholesterol-conjugated RNAi trigger (chol-RNAi) to selectively degrade AAT mRNA by RNAi and a melittin-derived peptide conjugated to N-acetylgalactosamine (NAG) formulated as the excipient EX1 to promote endosomal escape of the chol-RNAi in hepatocytes.
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Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
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