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Merck
CN

D26202

3,5-二氨基-1,2,4-三氮唑

98%

别名:

胍唑

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关于此项目

经验公式(希尔记法):
C2H5N5
化学文摘社编号:
分子量:
99.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
215-937-2
Beilstein/REAXYS Number:
112467
MDL number:
Assay:
98%
Form:
solid
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InChI

1S/C2H5N5/c3-1-5-2(4)7-6-1/h(H5,3,4,5,6,7)

InChI key

PKWIYNIDEDLDCJ-UHFFFAOYSA-N

SMILES string

Nc1n[nH]c(N)n1

assay

98%

form

solid

mp

202-205 °C (lit.)

Quality Level

General description

3,5-二氨基-1,2,4-三唑,别名胍唑,是杂环化合物,常作为合成砌块制备叔丁基取代无环和环状化合物的镓络合物。也用作铜的缓蚀剂。

Application

DNA 合成抑制剂。

pictograms

Health hazardEnvironment

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Repr. 2 - STOT RE 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Chlamydiae are obligate intracellular bacteria that are dependent on eukaryotic host cells for ribonucleoside triphosphates but not deoxyribonucleotide triphosphates. Ribonucleotide reductase is the only enzyme known to catalyze the direct conversion of a ribonucleotide to a deoxyribonucleotide. Hydroxyurea inhibits ribonucleotide
R G Hards et al.
Journal of cellular physiology, 106(2), 309-319 (1981-02-01)
We describe the isolation and characterization of a Chinese hamster ovary cell line selected for resistance to N-carbamoyloxyurea. Using the mammalian cell permeabilization assay developed in our laboratory, a detailed analysis of the target enzyme, ribonucleotide reductase (EC 1.17.4.1), was
Studies on the selective toxicity of guanazole in mice.
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European journal of cancer, 14(1), 33-40 (1978-01-01)
[Pharmacokinetics of antitumor drugs].
V A Filov et al.
Voprosy onkologii, 29(7), 3-13 (1983-01-01)
Inhibition of ribonucleotide reductases encoded by herpes simplex viruses.
T Spector
Pharmacology & therapeutics, 31(3), 295-302 (1985-01-01)

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