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D7408

Sigma-Aldrich

2′,5′-Dideoxyadenosine

≥95% (HPLC), solid

Sinonimo/i:

2ʹ,5ʹ-dd-Ado, NSC 95943

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About This Item

Formula empirica (notazione di Hill):
C10H13N5O2
Numero CAS:
Peso molecolare:
235.24
Numero MDL:
Codice UNSPSC:
41106305
ID PubChem:
NACRES:
NA.77

Saggio

≥95% (HPLC)

Forma fisica

solid

Colore

white

Solubilità

DMSO: soluble

Temperatura di conservazione

−20°C

Stringa SMILE

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
FFHPXOJTVQDVMO-DSYKOEDSSA-N

Informazioni sul gene

Applicazioni

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

Azioni biochim/fisiol

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

Caratteristiche e vantaggi

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.

Ricostituzione

Store at −20 °C after reconstitution.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


Certificati d'analisi (COA)

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