5-CARBOXYCYTOSINE
5-CARBOXYCYTOSINE ??
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256-257 °C
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1.88±0.1 g/cm3(Predicted)
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Refrigerator, under inert atmosphere
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?? ?? (pKa)
-3.50±0.20(Predicted)
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IRRITANT
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KE-09369
????(GHS):
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Warning
??·?? ??:
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P- ??
H302
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?? 4
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P264, P270, P301+P312, P330, P501
H315
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?? 2
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P264, P280, P302+P352, P321,P332+P313, P362
H319
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?? 2A
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P264, P280, P305+P351+P338,P337+P313P
H335
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?? 3
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P261
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P301+P312
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P302+P352
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P304+P340
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P305+P351+P338
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5-CARBOXYCYTOSINE C??? ??, ??, ??
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Cytosine derivatives, such as 5-Carboxylcytosine, are involved with a wide variety of biological functions including cytosine methylation, gene expression, genome stability, and chromatin modification. In addition, 5-Carboxylcytosine interacts with the RNA polymerase II elongation complex that can influence the pluripotent states during early embryonic development.
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ChEBI: A nucleobase analogue that is cytosine in which the hydrogen at position 5 is replaced by a carboxy group.
5-CARBOXYCYTOSINE ?? ?? ? ???
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5-CARBOXYCYTOSINE ?? ??
???( 40)?? ??
China 29
Germany 1
United Kingdom 3
United States 7
Global 40
5-CARBOXYCYTOSINE ?? ??:
??? 5-?????
6-(HYDROXYMETHYL)URACIL
2,4-Dihydroxypyrimidine-5-carboxylic acid
2-(2-chloropyriMidin-5-yl)propan-2-ol
5,6-Diamino-1,3-dimethyluracil hydrate
dihydro-6-imino-1,3-dimethyl-3H-pyrimidine-2,4,5-trione 5-oxime
(E)-5-(2-BROMOVINYL)URACIL
OROTIC ACID MONOHYDRATE
dihydro-6-imino-1,3-dimethyluracil
6-FORMYL-URACIL MONOHYDRATE
Pyrimidine, 4-(chloromethyl)-2,6-dimethoxy-
Tetrahydrofuryluracil
Pyrimidine, 5-chloro-4-(chloromethyl)-2,6-dimethoxy-
5-Pyrimidinecarboxylic acid
5-CARBOXYCYTOSINE
Pyrimidine-5-carboxaldehyde
2-Hydroxypyrimidine