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Merck
CN

13155

Sigma-Aldrich

N6-苄基腺苷

≥99.0%

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About This Item

经验公式(希尔记法):
C17H19N5O4
CAS号:
分子量:
357.36
Beilstein:
56815
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

质量水平

检测方案

≥99.0%

形式

powder

mp

184-186 °C

储存温度

2-8°C

SMILES字符串

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(NCc4ccccc4)ncnc23

InChI

1S/C17H19N5O4/c23-7-11-13(24)14(25)17(26-11)22-9-21-12-15(19-8-20-16(12)22)18-6-10-4-2-1-3-5-10/h1-5,8-9,11,13-14,17,23-25H,6-7H2,(H,18,19,20)/t11-,13-,14-,17-/m1/s1

InChI key

MRPKNNSABYPGBF-LSCFUAHRSA-N

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WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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B C Froehler et al.
Nucleic acids research, 11(22), 8031-8036 (1983-11-25)
Sterically hindered N6-dialkylformamidine protected deoxyadenosine is more stable to acidic depurination than N6-benzoyldeoxyadenosine and is potentially a valuable protecting group in the synthesis of deoxyoligonucleotides.
Karel Dolezal et al.
Bioorganic & medicinal chemistry, 15(11), 3737-3747 (2007-04-10)
Cytokinin activity of forty-eight 6-benzyladenosine derivatives at both the receptor and cellular levels as well as their anticancer properties were compared in various in vitro assays. The compounds were prepared by the condensation of 6-chloropurine riboside with corresponding substituted benzylamines
R G Luiten et al.
Nucleic acids research, 11(22), 8073-8085 (1983-11-25)
From in vitro protein synthesis studies and nucleotide sequence analysis it has been deduced that, unlike the major coat proteins of the hitherto studied filamentous bacterial viruses Ff (M13, fd and f1), IKe and Pf1, the major coat protein of
P Mlejnek
Journal of cellular biochemistry, 83(4), 678-689 (2001-12-18)
As an extension of our recently published work (Mlejnek and Kuglík [2000] J. Cell. Biochem. 77:6-17), the role of caspases in N(6)-benzylaminopurine riboside (BAPR)-induced apotosis in HL-60 cells was evaluated in this study. Here, BAPR-induced apoptosis was accompanied by activation
Young Ah Kim et al.
Biochemical pharmacology, 73(10), 1558-1572 (2007-02-20)
Toxoplasma gondii is an opportunistic pathogen responsible for toxoplasmosis. T. gondii is a purine auxotroph incapable of de novo purine biosynthesis and depends on salvage pathways for its purine requirements. Adenosine kinase (EC.2.7.1.20) is the major enzyme in the salvage

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