2'-Deoxy-N-methyl-AMP

Cat. No.: HY-177787: Data Sheet Handling Instructions
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2'-Deoxy-N-methyl-AMP is a highly efficient substrate for N6-methyl-AMP aminohydrolase. 2'-Deoxy-N-methyl-AMP has high catalytic efficiency. 2'-Deoxy-N-methyl-AMP can be used for research on cancer and viral infections.

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

2'-Deoxy-N-methyl-AMP Chemical Structure

CAS No. : 53696-69-8

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This product is a controlled substance and not for sale in your territory.

Other In-stock Forms of 2'-Deoxy-N-methyl-AMP:

2'-Deoxy-N-methyl-AMP ammonium

Other Forms of 2'-Deoxy-N-methyl-AMP:

2'-Deoxy-N-methyl-AMP ammonium In-stock

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Biological Activity
Purity & Documentation
References
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Description

Molecular Weight

345.25

Formula

C₁₁H₁₆N₅O₆P

CAS No.

53696-69-8

SMILES

O[C@H]1C[C@H](N(C=N2)C3=C2C(NC)=NC=N3)O[C@@H]1COP(O)(O)=O

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Solvent & Solubility

In Vitro:

H₂O : 50 mg/mL (144.82 mM; Need ultrasonic)

Preparing
Stock Solutions

Concentration Solvent Mass	1 mg	5 mg	10 mg

1 mM	2.8965 mL	14.4823 mL	28.9645 mL
5 mM	0.5793 mL	2.8965 mL	5.7929 mL
10 mM	0.2896 mL	1.4482 mL	2.8965 mL

View the Complete Stock Solution Preparation Table

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

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Working solution concentration: mg/mL

This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.

The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).

Purity & Documentation

Handling Instructions (2659 KB)

References

[1]. Schinkmanová M, et al. N6-methyl-AMP aminohydrolase activates N6-substituted purine acyclic nucleoside phosphonates. Biochem Pharmacol. 2006 Apr 28;71(9):1370-6. [Content Brief]

[2]. Yi Yang, et al. Site-specific glycoprotein conjugates and methods for making the same. WO2023065137.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

H₂O	1 mM	2.8965 mL	14.4823 mL	28.9645 mL	72.4113 mL
	5 mM	0.5793 mL	2.8965 mL	5.7929 mL	14.4823 mL
	10 mM	0.2896 mL	1.4482 mL	2.8965 mL	7.2411 mL
	15 mM	0.1931 mL	0.9655 mL	1.9310 mL	4.8274 mL
	20 mM	0.1448 mL	0.7241 mL	1.4482 mL	3.6206 mL
	25 mM	0.1159 mL	0.5793 mL	1.1586 mL	2.8965 mL
	30 mM	0.0965 mL	0.4827 mL	0.9655 mL	2.4137 mL
	40 mM	0.0724 mL	0.3621 mL	0.7241 mL	1.8103 mL
	50 mM	0.0579 mL	0.2896 mL	0.5793 mL	1.4482 mL
	60 mM	0.0483 mL	0.2414 mL	0.4827 mL	1.2069 mL
	80 mM	0.0362 mL	0.1810 mL	0.3621 mL	0.9051 mL
	100 mM	0.0290 mL	0.1448 mL	0.2896 mL	0.7241 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.