2'-Deoxyadenosine-5'-monophosphate-¹³C₁₀,¹⁵N₅ dilithium

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2'-Deoxyadenosine-5'-monophosphate-¹³C₁₀,¹⁵N₅ dilithium is ¹³C and 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.

For research use only. We do not sell to patients.

2'-Deoxyadenosine-5'-monophosphate-<sup>13</sup>C<sub>10</sub>,<sup>15</sup>N<sub>5</sub> dilithium Chemical Structure

2'-Deoxyadenosine-5'-monophosphate-¹³C₁₀,¹⁵N₅ dilithium Chemical Structure

CAS No. : 2483830-51-7

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1 mg		Get quote	Estimated Time of Arrival: December 31

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Other Forms of 2'-Deoxyadenosine-5'-monophosphate-¹³C₁₀,¹⁵N₅ dilithium:

2'-Deoxyadenosine-5'-monophosphate Get quote
2'-Deoxyadenosine-5'-monophosphate-d₁₂ dilithium Get quote
2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅,d₁₂ dilithium Get quote
2'-Deoxyadenosine-5'-monophosphate-¹⁵N₅ dilithium Get quote
2'-Deoxyadenosine-5'-monophosphate-¹³C₁₀ dilithium Get quote

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Description	2'-Deoxyadenosine-5'-monophosphate-¹³C₁₀,¹⁵N₅ dilithium is ¹³C and 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.
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-¹³C₁₀,¹⁵N₅ dilithium Related Antibodies
Molecular Weight	357.98
Formula	¹³C₁₀H₁₂Li₂¹⁵N₅O₆P
CAS No.	2483830-51-7
SMILES	O=P(O[Li])(O[Li])O[13CH2][13C@H]1O[13C@@H]([15N]2[13C]3=[15N][13CH]=[15N][13C]([15NH2])=[13C]3[15N]=[13CH]2)[13CH2][13C@@H]1O
Shipping	Room temperature in continental US; may vary elsewhere.
Storage	Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation	Data Sheet (278 KB) Handling Instructions (2659 KB)
References	[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]