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D7408

Sigma-Aldrich

2′,5′-Dideoxyadenosine

≥95% (HPLC), solid

Sinónimos:

2ʹ,5ʹ-dd-Ado, NSC 95943

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About This Item

Fórmula empírica (notación de Hill):
C10H13N5O2
Número de CAS:
6698-26-6
Peso molecular:
235.24
Número MDL:
MFCD00210904
Código UNSPSC:
41106305
ID de la sustancia en PubChem:
24894132
NACRES:
NA.77

Nivel de calidad

100

Análisis

≥95% (HPLC)

formulario

solid

color

white

solubilidad

DMSO: soluble

temp. de almacenamiento

−20°C

cadena SMILES

C[C@H]1O[C@H](C[C@@H]1O)n2cnc3c(N)ncnc23

InChI

1S/C10H13N5O2/c1-5-6(16)2-7(17-5)15-4-14-8-9(11)12-3-13-10(8)15/h3-7,16H,2H2,1H3,(H2,11,12,13)/t5-,6+,7-/m1/s1

Clave InChI

FFHPXOJTVQDVMO-DSYKOEDSSA-N

Información sobre el gen

rat ... Adcy2(81636)

Aplicación

2′,5′-Dideoxyadenosine has been used to elucidate the mechanism of diligustilide (DLG). It has also been used to inhibit adenylate cyclase (AC).

Acciones bioquímicas o fisiológicas

Cell-permeable adenylyl cyclase inhibitor. IC50 = 2.7 μM in detergent-dispersed rat brain preparations.

Características y beneficios

This compound is a featured product for Cyclic Nucleotide research. Click here to discover more featured Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Adenylyl cyclases page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Reconstitución

Store at −20 °C after reconstitution.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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