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D7408

Sigma-Aldrich

2′,5′-Dideoxyadenosine

≥95% (HPLC), solid

Synonyme(s) :

2ʹ,5ʹ-dd-Ado, NSC 95943

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About This Item

Formule empirique (notation de Hill):
C10H13N5O2
Numéro CAS:
6698-26-6
Poids moléculaire :
235.24
Numéro MDL:
MFCD00210904
Code UNSPSC :
41106305
ID de substance PubChem :
24894132
Nomenclature NACRES :
NA.77

Pureté

≥95% (HPLC)

Forme

solid

Couleur

white

Solubilité

DMSO: soluble

Température de stockage

−20°C

Chaîne 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

Clé InChI

FFHPXOJTVQDVMO-DSYKOEDSSA-N

Informations sur le gène

rat ... Adcy2(81636)

Application

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

Actions biochimiques/physiologiques

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

Caractéristiques et avantages

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.

Reconstitution

Store at −20 °C after reconstitution.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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