| Identification | More | [Name]
Adenine hydrochloride | [CAS]
2922-28-3 | [Synonyms]
1H-Purin-6-amine monohydrochloride
6-AMINOPURINE HCL
6-AMINOPURINE HYDROCHLORIDE
ADENINE HCL
ADENINE HYDROCHLORIDE
ADENINE MONOHYDROCHLORIDE
ADENINIUM CHLORIDE
TIMTEC-BB SBB003841
6-Aminopurine hydrochloride anhydrous
Adenine hydrochloride anhydrous
Adenine hydrochloride, 98%, cont. up to ca 5% water | [EINECS(EC#)]
220-867-0 | [Molecular Formula]
C5H6ClN5 | [MDL Number]
MFCD00075782 | [Molecular Weight]
171.59 | [MOL File]
2922-28-3.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [F ]
3-8 | [TSCA ]
Yes | [HS Code ]
29335990 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powder | [Uses]
Adenine hydrochloride hydrate has been used:
- As a component of FAD cell culture media
- In maintaining organotypic cultures for recreating stratified epithelium from primary cell cultures
- In limbal-corneal epithelial culturing and keratinocytes
| [Uses]
Adenine is a purine nucleobase with a wide range of chemical and biochemical roles in vivo and in vitro. It is a regulatory molecule and a component of DNA, RNA, cofactors (NAD, FAD) and signaling molecules (cAMP). | [Biological Activity]
adenine hcl, a purine derivative and a nucleobase, plays crucial roles in substantial biochemistry processes in vivo, including cellular respiration, formation of the energy-rich adenosine triphosphate (atp), the cofactors nicotinamide adenine dinucleotide (nad) and flavin adenine dinucleotide (fad) as well as protein synthesis. in addition, adenine hcl also serves as a chemical component of dna and rna. adenosine triphosphate is used in cellular metabolism as one of the basic methods of transferring chemical energy between chemical reactions. [1] | [in vitro]
the cyto-protective effect of adenosine was measured using an in vitro model of acute tubular necrosis in rat kidney tubular cells. the finding suggested that adenosine at the concentration of 100 m could significantly decrease cellular injury. the ec50 value of adenosine was detected to be 14 m. [2] | [in vivo]
a study was performed to investigate the effects of dietary adenine on fatty liver induced by orotic acid (oa) in rats. 1% oa-supplemented diets with/ without 0.25% adenine was administered to rats for 10 days. enzyme assay kits were then applied to measure serum lipid profiles of tested rats, such as liver lipid concentrations in different treatment groups. moreover, the activities of fatty acid synthase (fas) and fatty acid β-oxidation were also detected. the findings suggested that addition of adenine to the diet offset the effect of oa and reversed promotion of liver tg content to basal level. administration of adenine also inhibited fas activities in rat liver. in conclusion, the ameliorating of fatty liver in adenine-treated rats was associated with the reduction of fas activities accompanied with the increase of mitochondrial fatty acid β-oxidation and the promotion of serum lipid secretion from the hepatic tissue into the bloodstream. [1] | [storage]
Store at -20°C | [References]
[1]buang y. dietary adenine alleviates fatty liver induced by orotic acid. indo. j. chem. 2010; 10 (3): 363 - 369.
[2] módis k, ger d, nagy n, szoleczky p, tóth zd and szabó c. cytoprotective effects of adenosine and inosine in an in vitro model of acute tubular necrosis. br j pharmacol. 2009 nov; 158(6): 1565–8. |
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J & K SCIENTIFIC LTD.
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Alfa Aesar
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Energy Chemical
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Maya High Purity Chemicals
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Spectrum Chemical Manufacturing Corp.
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021-021-021-67601398-809-809-809 15221380277 |
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