855049
5-Azacytosine
Synonym(s):
2-Hydroxy-4-aminotriazine, 4-Amino-1,3,5-triazin-2-ol, 4-Amino-1,3,5-triazin-2-one, 4-Amino-2-hydroxy-1,3,5-triazine, NSC 51100, NSC 54006
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About This Item
Empirical Formula (Hill Notation):
C3H4N4O
CAS Number:
Molecular Weight:
112.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-242-9
Beilstein/REAXYS Number:
116378
MDL number:
InChI key
MFEFTTYGMZOIKO-UHFFFAOYSA-N
InChI
1S/C3H4N4O/c4-2-5-1-6-3(8)7-2/h1H,(H3,4,5,6,7,8)
SMILES string
NC1=NC(=O)NC=N1
form
powder
mp
>300 °C (lit.)
Quality Level
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Application
Reactant for:
- Enzymic synthesis of nucleoside analogs using immobilized 2′-deoxyribosyltransferase from Lactobacillus reuteri
- Reactions with oxide radical ion
- Potential antitumor and antiproliferative agent against human leukemia cells
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type N95 (US)
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Mariana B Méndez et al.
AMB Express, 10(1), 173-173 (2020-09-30)
A novel IDA-LaNDT derivative was able to reach the highest productivity in the biosynthesis of a well-known antitumoral agent called decitabine. However, the combination of two simple and inexpensive techniques such as ionic absorption and gel entrapment with the incorporation
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