708-79-2
708-79-2
Chemical Structure
1-Methyluric acid
- CAS. Nr.: 708-79-2
- Formula:C6H6N4O3
- Molecular Weight:182.14
IUPAC Name: 2,8-dihydroxy-1-methyl-1,9-dihydro-6H-purin-6-one
InChIKey: QFDRTQONISXGJA-UHFFFAOYSA-N
SMILES: CN(C(O)=N1)C(C2=C1NC(O)=N2)=O
Biological Activity: 1-Methyluric acid acts on the urinary bladder mucosa and increases the blood glucose, insulin, triglyceride, and cholesterol levels.
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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1-Methyluric acid | 98.12% | 1-Methyluric acid acts on the urinary bladder mucosa and increases the blood glucose, insulin, triglyceride, and cholesterol levels. | ||||||||||||||||||||
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1-Methyluric acid-13C4,15N3 | 1-Methyluric acid-13C4,15N3 is the 13C and 15N labeled 1-Methyluric acid. 1-Methyluric acid acts on the urinary bladder mucosa and increases the blood glucose, insulin, triglyceride, and cholesterol levels. | |||||||||||||||||||||
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1-Methyluric acid-d3 | 96.02% | 1-Methyluric acid-d3 is the deuterium labeled 1-Methyluric acid (HY-W010031). 1-Methyluric acid acts on the urinary bladder mucosa and increases the blood glucose, insulin, triglyceride, and cholesterol levels. | ||||||||||||||||||||
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9-Methylguanine | 9-Methylguanine, a derivative of 8-mercaptoguanine, is a dihydropteroate synthase (DHPS) inhibitor with a Kd of 58 μM for E.coli DHPS (EcDHPS). | |||||||||||||||||||||
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8-Aminoguanine | 97.19% | 8-Aminoguanine is a endogenous purine. 8-Aminoguanine inhibits PNPase (purine nucleoside phosphorylase). 8-Aminoguanine induces diuresis/natriuresis/glucosuria. | ||||||||||||||||||||
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1-Methylxanthine (Standard) | ≥98% | 1-Methylxanthine (Standard) is the analytical standard of 1-Methylxanthine. This product is intended for research and analytical applications. 1-Methylxanthine, a caffeine derivative, is an essential human urinary metabolite of caffeine and theophylline (1,3-dimethylxanthine, TP). 1-Methylxanthine enhances the radiosensitivity of tumor cells. | ||||||||||||||||||||
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1-Methylxanthine-13C4,15N3 | 1-Methylxanthine-13C4,15N3 is the 13C-labeled and 15N-labeled 1-Methylxanthine. 1-Methylxanthine, a caffeine derivative, is an essential human urinary metabolite of caffeine and theophylline (1,3-dimethylxanthine, TP). 1-Methylxanthine enhances the radiosensitivity of tumor cells. | |||||||||||||||||||||
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8-Chlorotheophylline (Standard) | 99.74% | 8-Chlorotheophylline (Standard) is the analytical standard of 8-Chlorotheophylline. This product is intended for research and analytical applications. | ||||||||||||||||||||
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Paraxanthine (Standard) | 99.77% | Paraxanthine (Standard) is the analytical standard of Paraxanthine. This product is intended for research and analytical applications. Paraxanthine, a caffeine metabolite, provides protection against Dopaminergic cell death via stimulation of Ryanodine Receptor Channels. | ||||||||||||||||||||
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Paraxanthine-13C4,15N3 | 99.80% | Paraxanthine-13C4,15N3 is the 13C-labeled and 15N-labeled Paraxanthine. Paraxanthine, a caffeine metabolite, provides protection against Dopaminergic cell death via stimulation of Ryanodine Receptor Channels. | ||||||||||||||||||||
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8-Bromotheophylline (Standard) | ≥98% | 8-Bromotheophylline (Standard) is the analytical standard of 8-Bromotheophylline. This product is intended for research and analytical applications. 8-Bromotheophylline can be used for the synthesis of the Oxazolo[2,3-f]purinediones, which are evaluated for their affinity at adenosine A1 and A2A receptors. | ||||||||||||||||||||
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1,9-Dimethylxanthine | 1,9-Dimethylxanthine is an adenosine receptor antagonist that has the activity of blocking the effects of adenosine on the central nervous system. 1,9-Dimethylxanthine enhances nerve excitability by regulating the adenosine system. 1,9-Dimethylxanthine is used as a pharmacological tool in research to help explore physiological and pathological processes related to adenosine. | |||||||||||||||||||||
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Thiouric Acid Sodium Salt Dihydrate-13C3 | Thiouric Acid Sodium Salt Dihydrate-13C3 is the 13C-labeled Thiouric Acid Sodium Salt Dihydrate. | |||||||||||||||||||||
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