161770-53-2
161770-53-2
Chemical Structure
Xanthine-15N2
- CAS No.: 161770-53-2
- Formula:C5H4N215N2O2
- Molecular Weight:154.10
IUPAC Name: 3,7-dihydro-1H-purine-2,6-dione-1,3-15N2
InChIKey: LRFVTYWOQMYALW-IOOOXAEESA-N
SMILES: O=C1C2=C(N=CN2)[15NH]C([15NH]1)=O
Biological Activity: Xanthine-15N2 is a 15N-labeled Xanthine (HY-W017389)[1]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Xanthine-15N2 | 99.35% | Xanthine-15N2 is a 15N-labeled Xanthine (HY-W017389). Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation. | ||||||||||||||||||||
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Xanthine (Standard) | 99.09% | Xanthine (Standard) is the analytical standard of Xanthine. This product is intended for research and analytical applications. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation. In Vitro: A number of stimulants are derived from Xanthine including caffeine and theobromine. Xanthine is a product on the pathway of purine degradation. Xanthine is subsequently converted to uric acid by the action of the Xanthine oxidase enzyme. | ||||||||||||||||||||
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Xanthine-13C,15N2 | 95.64% | Xanthine-13C,15N2 is a 15N-labeled and 13C-labled Xanthine (HY-W017389). Xanthine is a plant alkaloid with mild stimulant activity of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation. | ||||||||||||||||||||
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Xanthine | 98.99% | Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation. | ||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-223. [Content Brief]
- [2]. Pundir CS, Devi R. Biosensing methods for xanthine determination: a review. Enzyme Microb Technol. 2014;57:55-62. [Content Brief]
- [3]. David A. Taylor, et al. Central Nervous SystemStimulants.
- [4]. Ashihara H, et al. Xanthine Alkaloids: Occurrence, Biosynthesis, and Function in Plants. Prog Chem Org Nat Prod. 2017;105:1-88. [Content Brief]
