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2-脱氧肌苷

中文名称:
2-脱氧肌苷
中文同义词:
2ˊ-脱氧次黄嘌呤核苷;2ˊ-脱氧肌苷;9-(2-脱氧-Β-D-呋喃核糖基)次黄嘌呤;9-(2-脱氧-Β-D-呋喃核糖)黄嘌呤;2-脱氧-肌苷 水合物;2-脱氧-肌苷一水合物;9-(2-脱氧-Β-D-呋喃核糖基)次黄嘌呤2-脱氧次黄嘌呤核苷2-脱氧肌苷;2-脱氧肌苷, 98+%
英文名称:
2-Deoxyinosine
英文同义词:
Didanosine EP Impurity C;Didanosine Impurity Ⅲ:2-Deoxyinosine;Didanosine Impurity 3(Didanosine EP Impurity C);2-Deoxyinosine;2-Deoxyinosine(Di);DEOXYINOSINE, 2-(RG);9-[(2R,4S,5R)-4-hydroxy-5-(hydroxyMethyl)oxolan-2-yl]-9H-purin-6-ol;9-((2R,4S,5R)-4-Hydroxy-5-(hydroxyMethyl)tetrahydrofuran-2-yl)-9H-purin-6-ol
CAS号:
890-38-0
分子式:
C10H12N4O4
分子量:
252.23
EINECS号:
212-964-1
相关类别:
医用原料;核苷;对照品;生化试剂-植物激素及核酸类;生化试剂;核酸;小分子抑制剂;其他生化试剂;化学试剂;Pharmaceutical Raw Materials;Pyridines, Pyrimidines, Purines and Pteredines;Biochemistry;Nucleosides and their analogs;Bases Related Reagents;Heterocycles;Impurities;Inhibitors;Intermediates Fine Chemicals;Nucleotides;Pharmaceuticals;Heterocycles, Impurities, Inhibitors, Nucleotides, Bases Related Reagents, Pharmaceuticals, Intermediates Fine Chemicals;植物激素及核酸类;核苷,核苷酸,寡核苷酸;医用原料;有机溶剂;对照品;中药对照品;Nucleosides, Nucleotides Related Reagents
Mol文件:
890-38-0.mol
熔点 
250 °C
比旋光度 
21 º (c=1, H2O 22 ºC)
沸点 
395.4°C (rough estimate)
密度 
1.3402 (rough estimate)
折射率 
-16 ° (C=1, H2O)
储存条件 
-20°C
酸度系数(pKa)
8.92±0.70(Predicted)
形态
Powder
颜色
White to Off-white
水溶解性 
8.33g/L(25.02 ºC)
BRN 
33517
CAS 数据库
890-38-0(CAS DataBase Reference)
NIST化学物质信息
Inosine, 2-deoxy-(890-38-0)
生物活性
2’-deoxyadenosine 能够抑制人癌细胞株的生长,并发现其与嘌呤核苷磷酸化酶 (PNP) 缺乏有关。
靶点
Human Endogenous Metabolite
Human Endogenous Metabolite
体外研究
In the absence of deoxycoformycin, 2’-deoxyadenosine is primarily deaminated to 2’-deoxyinosine and then converted into hypoxanthine. In the presence of the inhibitor, the deoxynucleoside, in addition to a phosphorylation process, undergoes phosphorolytic cleavage giving rise to adenine. The conversion of 2’-deoxyadenosine to adenine might represent a protective device, emerging when the activity of adenosine deaminase is reduced or inhibited. There is much evidence to indicate that the enzyme catalyzing this processs may be distinct from methylthioadenosine phosphorylase and S-adenosyl homocysteine hydrolase, which are the enzymes reported to be responsible for the formation of adenine from 28-deoxyadenosine in mammals.
化学性质 
白色粉末,可溶于甲醇、乙醇、DMSO等有机溶剂。
危险品标志 
Xn,Xi
危险类别码 
20/21/22-36/37/38
安全说明 
24/25-37/39-36-26
WGK Germany 
3
10-23
海关编码 
29349990
CAS号:890-38-0
规   格:10g/20g/100g/1kg
价   格:请咨询卖家
数   量:
联系方式
 15623309010
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正规发票
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英文名:2-Deoxyinosine
外观:
纯度:请咨询卖家
分子式:C10H12N4O4
分子量:252.23
最小起售量:10g/20g/100g/1kg
中文名称:
2-脱氧肌苷
中文同义词:
2ˊ-脱氧次黄嘌呤核苷;2ˊ-脱氧肌苷;9-(2-脱氧-Β-D-呋喃核糖基)次黄嘌呤;9-(2-脱氧-Β-D-呋喃核糖)黄嘌呤;2-脱氧-肌苷 水合物;2-脱氧-肌苷一水合物;9-(2-脱氧-Β-D-呋喃核糖基)次黄嘌呤2-脱氧次黄嘌呤核苷2-脱氧肌苷;2-脱氧肌苷, 98+%
英文名称:
2-Deoxyinosine
英文同义词:
Didanosine EP Impurity C;Didanosine Impurity Ⅲ:2-Deoxyinosine;Didanosine Impurity 3(Didanosine EP Impurity C);2-Deoxyinosine;2-Deoxyinosine(Di);DEOXYINOSINE, 2-(RG);9-[(2R,4S,5R)-4-hydroxy-5-(hydroxyMethyl)oxolan-2-yl]-9H-purin-6-ol;9-((2R,4S,5R)-4-Hydroxy-5-(hydroxyMethyl)tetrahydrofuran-2-yl)-9H-purin-6-ol
CAS号:
890-38-0
分子式:
C10H12N4O4
分子量:
252.23
EINECS号:
212-964-1
相关类别:
医用原料;核苷;对照品;生化试剂-植物激素及核酸类;生化试剂;核酸;小分子抑制剂;其他生化试剂;化学试剂;Pharmaceutical Raw Materials;Pyridines, Pyrimidines, Purines and Pteredines;Biochemistry;Nucleosides and their analogs;Bases Related Reagents;Heterocycles;Impurities;Inhibitors;Intermediates Fine Chemicals;Nucleotides;Pharmaceuticals;Heterocycles, Impurities, Inhibitors, Nucleotides, Bases Related Reagents, Pharmaceuticals, Intermediates Fine Chemicals;植物激素及核酸类;核苷,核苷酸,寡核苷酸;医用原料;有机溶剂;对照品;中药对照品;Nucleosides, Nucleotides Related Reagents
Mol文件:
890-38-0.mol
熔点 
250 °C
比旋光度 
21 º (c=1, H2O 22 ºC)
沸点 
395.4°C (rough estimate)
密度 
1.3402 (rough estimate)
折射率 
-16 ° (C=1, H2O)
储存条件 
-20°C
酸度系数(pKa)
8.92±0.70(Predicted)
形态
Powder
颜色
White to Off-white
水溶解性 
8.33g/L(25.02 ºC)
BRN 
33517
CAS 数据库
890-38-0(CAS DataBase Reference)
NIST化学物质信息
Inosine, 2-deoxy-(890-38-0)
生物活性
2’-deoxyadenosine 能够抑制人癌细胞株的生长,并发现其与嘌呤核苷磷酸化酶 (PNP) 缺乏有关。
靶点
Human Endogenous Metabolite
Human Endogenous Metabolite
体外研究
In the absence of deoxycoformycin, 2’-deoxyadenosine is primarily deaminated to 2’-deoxyinosine and then converted into hypoxanthine. In the presence of the inhibitor, the deoxynucleoside, in addition to a phosphorylation process, undergoes phosphorolytic cleavage giving rise to adenine. The conversion of 2’-deoxyadenosine to adenine might represent a protective device, emerging when the activity of adenosine deaminase is reduced or inhibited. There is much evidence to indicate that the enzyme catalyzing this processs may be distinct from methylthioadenosine phosphorylase and S-adenosyl homocysteine hydrolase, which are the enzymes reported to be responsible for the formation of adenine from 28-deoxyadenosine in mammals.
化学性质 
白色粉末,可溶于甲醇、乙醇、DMSO等有机溶剂。
危险品标志 
Xn,Xi
危险类别码 
20/21/22-36/37/38
安全说明 
24/25-37/39-36-26
WGK Germany 
3
10-23
海关编码 
29349990
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