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Merck
CN

766755

Sigma-Aldrich

2,6-Diaminopurine-9-arabinoside

97%

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别名:
2,6-Diamino-9-(β-D-arabinofuranosyl)purine
经验公式(希尔记法):
C10H14N6O4
CAS号:
分子量:
282.26
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

形式

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.

象形图

Skull and crossbones

警示用语:

Danger

危险声明

预防措施声明

危险分类

Acute Tox. 3 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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[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
[Antiviral effects of 9-beta-D-arabinofuranosyl-2,6-diaminopurine against experimental herpetic keratitis].
S Yamane
Nippon Ganka Gakkai zasshi, 88(3), 586-594 (1984-03-01)

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