2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅ dilithium

Cat. No.: HY-W016009S2: Ficha de datos Instrucciones de manejo
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2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅ dilithium is ¹⁵N labeled 2'-Deoxyadenosine-5'-monophosphate (HY-W016009). 2′-Deoxyadenosine 5′-monophosphate, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate can be used to study adenosine-based interactions during DNA synthesis and DNA damage.

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2'-Deoxyadenosine-5'-monophosphate-<sup>15</sup>N<sub>5</sub> dilithium

2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅ dilithium Estructura química

Tamaño		Stock
1 mg		Obtener un presupuesto	Estimated Time of Arrival: December 31

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Other Forms of 2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅ dilithium:

2'-Deoxyadenosine-5'-monophosphate In-stock
2'-Deoxyadenosine-5'-monophosphate-d₁₂ dilithium In-stock
2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅,d₁₂ dilithium Obtener un presupuesto
2'-Deoxyadenosine-5'-monophosphate-¹³C₁₀ dilithium Obtener un presupuesto
2'-Deoxyadenosine-5'-monophosphate-¹³C₁₀,¹⁵N₅ dilithium Obtener un presupuesto

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Descripciòn	2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅ dilithium is ¹⁵N labeled 2'-Deoxyadenosine-5'-monophosphate (HY-W016009). 2′-Deoxyadenosine 5′-monophosphate, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate can be used to study adenosine-based interactions during DNA synthesis and DNA damage.
Application	1. This compound can be used as a tracer. 2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
In Vitro	Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs^[1]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. 2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅ dilithium Related Antibodies
Peso molecular	348.05
Fòrmula	C₁₀H₁₂Li₂¹⁵N₅O₆P
SMILES	O=P(O[Li])(O[Li])OC[C@H]1O[C@@H]([15N]2C([15N]=C[15N]=C3[15NH2])=C3[15N]=C2)C[C@@H]1O
Envío	Room temperature in continental US; may vary elsewhere.
Almacenamiento	Please store the product under the recommended conditions in the Certificate of Analysis.
Pureza y Documentación	Ficha de datos (271 KB) Instrucciones de manejo (2659 KB)
Referencias	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief] [2]. Katsuya Narumi, et al. Mutual role of ecto-5'-nucleotidase/CD73 and concentrative nucleoside transporter 3 in the intestinal uptake of dAMP. PLoS One. 2019 Oct 21;14(10):e0223892. [Content Brief] [3]. V Duarte, et al. Insertion of dGMP and dAMP during in vitro DNA synthesis opposite an oxidized form of 7,8-dihydro-8-oxoguanine. Nucleic Acids Res. 1999 Jan 15;27(2):496-502. [Content Brief]