所有图片(2)
About This Item
经验公式（希尔记法）:
C10H14N6O4
CAS号:
分子量:
282.26
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.22
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方案
97%
表单
solid
旋光性
[α]22/D +28.5°, c = 0.5% in hydrochloric acid
mp
286-290 °C
储存温度
2-8°C
SMILES字符串
Nc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@@H]3O)c2n1
InChI
1S/C10H14N6O4/c11-7-4-8(15-10(12)14-7)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H4,11,12,14,15)/t3-,5-,6+,9-/m1/s1
InChI key
ZDTFMPXQUSBYRL-FJFJXFQQSA-N
应用
Versatile nucleoside intermediate.
警示用语：
Danger
危险声明
预防措施声明
危险分类
Acute Tox. 3 Oral
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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Nippon Ganka Gakkai zasshi, 88(3), 586-594 (1984-03-01)
[Comparative studies of anti-herpes simplex virus compounds in vitro].
S Inoue et al.
Nippon Ganka Gakkai zasshi, 86(11), 2113-2121 (1982-01-01)
S Bajaj et al.
Blood, 62(1), 75-80 (1983-07-01)
We compared the effect of adenosine and adenosine analogues on the phytohemagglutinin-induced proliferative response of blood lymphocytes from normal subjects and patients with chronic lymphocytic leukemia. As measured by the inhibition of thymidine or leucine incorporation, adenosine was more toxic
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