![]() 6-n-hydroxyadenosine structure
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Common Name | 6-n-hydroxyadenosine | ||
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CAS Number | 3414-62-8 | Molecular Weight | 283.24100 | |
Density | 2.12g/cm3 | Boiling Point | 703.7ºC at 760 mmHg | |
Molecular Formula | C10H13N5O5 | Melting Point | N/A | |
MSDS | N/A | Flash Point | 379.4ºC |
Use of 6-n-hydroxyadenosineInosine oxime (6-Hydroxyadenosine) is an endogenous metabolite in the course of cell metabolism by cytochrome P450, by oxidative stress or by deviating nucleotide biosynthesis. Inosine oxime has toxic and mutagenic for procaryotic and eucaryotic cells[1][2]. |
Name | 6-n-hydroxyadenosine |
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Synonym | More Synonyms |
Description | Inosine oxime (6-Hydroxyadenosine) is an endogenous metabolite in the course of cell metabolism by cytochrome P450, by oxidative stress or by deviating nucleotide biosynthesis. Inosine oxime has toxic and mutagenic for procaryotic and eucaryotic cells[1][2]. |
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Related Catalog | |
In Vitro | Inosine oxime (6-Hydroxyadenosine) (1-5 nM) has reductive detoxication through direct dehydroxylamination catalyzed by adenosine deaminase to inosine and decreases inosine formation by 35% with knockdown of mARC1 in HEK-293. |
References |
Density | 2.12g/cm3 |
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Boiling Point | 703.7ºC at 760 mmHg |
Molecular Formula | C10H13N5O5 |
Molecular Weight | 283.24100 |
Flash Point | 379.4ºC |
Exact Mass | 283.09200 |
PSA | 149.01000 |
Index of Refraction | 1.897 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Precursor 0 | |
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DownStream 1 | |
N6-Hydroxy-5-methyl-cytosin |
N6-hydroxyadenosine |
N-hydroxyadenosine |
5-methyl-1H-pyrimidine-2,4-dione 4-oxime |
6-(hydroxyamino)-5-methylpyrimidin-2(1h)-one |
5-Methyl-N(4)-hydroxycytosine |