Copy Link Print Information

Bampidirsen

(Synonyms: WVE-N531)

Bampidirsen (WVE-N531) is an antisense oligonucleotide (ASO) with a phosphorodiamidate backbone. Bampidirsen specifically induces DMD exon 53 skipping, and it can be used for the research of Duchenne muscular dystrophy.

Para uso exclusivo en investigación. No vendemos a pacientes.

  • No. CAS: 2379448-61-8
  • Fòrmula: C206H250F17N78O109P19S14
  • Peso molecular:6923.02
  • Almacenamiento:

    Please store the product under the recommended conditions in the Certificate of Analysis.

  • Bampidirsen Chemical Structure
    Bampidirsen Chemical Structure
No. CAS: 2379448-61-8
Tamaño
Precio
Stock
Cantidad
Amount: USD 0.00
Please select quantity
or
or

* Seleccione Cantidad antes de agregar artículos.

To place orders, for customer services and technical support, please contact: MedChemExpress USA

Tel: 609-228-6898 E-mail: [email protected] [email protected]

Data Download

To place orders, for customer services and technical support, please contact:

609-228-6898
[email protected] [email protected]
Encuentre su distribuidor local Your local distributor: Hycultec GmbHHycultec
  • Actividad biológica
  • Chemical Information
  • Pureza y Documentación
  • Referencias
  • Help & FAQs
Top Publications Citing

Use of MCE Products

Keywords

MOQ
Minimum order quantity
100 mg

Obtener un presupuesto En stock

Other size
Obtener un presupuesto
Please select quantity
Amount: USD 0.00
Sign in to MedChemExpress Inicie sesiòn
Registrar
Sign in to MedChemExpress
Registrar una cuenta nueva

At least 6 characters

Personalize your experience, you are currently not signed in. For a better experience, please create an online profile, you can:

Obtain points redemption prizes
Check out faster
Add multiple shipping locations
View orders
Assay Types
  • Bampidirsen Chemical Structure
    Bampidirsen Chemical Structure RNA, ((2′-deoxy-2′-fluoro)(C-[P(S)]-sp-U-[P(S)]-sp-C-[P(R)]-P-deoxy-P-[(1,3-dimethyl-2-imidazolidinylidene)amino]-C-[P(S)]-sp-G-[P(S)]-sp-G-[P(R)]-P-deoxy-P-[(1,3-dimethyl-2-imidazolidinylidene)amino]-U-[P(S)]-sp-U)-[P(S)]-sp-Cm-(2′-deoxy-2′-fluoro)U-[P(S)]-sp-Gm-[P(S)]-sp-(2′-deoxy-2′-fluoro)A-[P(S)]-sp-Am-(2′-deoxy-2′-fluoro)(G-[P(S)]-sp-G-[P(S)]-sp-U-[P(S)]-sp-G-[P(R)]-P-deoxy-P-[(1,3-dimethyl-2-imidazolidinylidene)amino]-U-[P(S)]-sp-U-[P(S)]-sp-C))
    1/16
  • RNA, ((2′-deoxy-2′-fluoro)(C-[P(S)]-sp-U-[P(S)]-sp-C-[P(R)]-P-deoxy-P-[(1,3-dimethyl-2-imidazolidinylidene)amino]-C-[P(S)]-sp-G-[P(S)]-sp-G-[P(R)]-P-deoxy-P-[(1,3-dimethyl-2-imidazolidinylidene)amino]-U-[P(S)]-sp-U)-[P(S)]-sp-Cm-(2′-deoxy-2′-fluoro)U-[P(S)]-sp-Gm-[P(S)]-sp-(2′-deoxy-2′-fluoro)A-[P(S)]-sp-Am-(2′-deoxy-2′-fluoro)(G-[P(S)]-sp-G-[P(S)]-sp-U-[P(S)]-sp-G-[P(R)]-P-deoxy-P-[(1,3-dimethyl-2-imidazolidinylidene)amino]-U-[P(S)]-sp-U-[P(S)]-sp-C))