8-羟基-2-脱氧鸟苷结构式
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常用名 | 8-羟基-2-脱氧鸟苷 | 英文名 | 8-hydroxy-2'-deoxyguanosine |
|---|---|---|---|---|
| CAS号 | 88847-89-6 | 分子量 | 283.241 | |
| 密度 | 2.3±0.1 g/cm3 | 沸点 | N/A | |
| 分子式 | C10H13N5O5 | 熔点 | 217-220ºC | |
| MSDS | 美版 | 闪点 | N/A |
8-羟基-2-脱氧鸟苷用途8-Hydroxy-2'-deoxyguanosine 是氧化应激和致癌反应的关键生物标志物。 |
| 中文名 | 8-羟基-2-脱氧鸟苷 |
|---|---|
| 英文名 | 8-hydroxy-2'-deoxyguanosine |
| 中文别名 | 8-羟基脱氧鸟苷 | 8-OH-脱氧鸟嘌呤 | 8-羟基-2'-脱氧鸟嘌呤 | 2'-脱氧-7,8-二氢-8-氧代鸟苷 |
| 英文别名 | 更多 |
| 描述 | 8-Hydroxy-2'-deoxyguanosine 是氧化应激和致癌反应的关键生物标志物。 |
|---|---|
| 相关类别 | |
| 靶点实验 |
Human Endogenous Metabolite |
| 体外研究 | 8-羟基-2'-脱氧鸟苷(8-OHdG)是用于各种癌症和退行性疾病的风险评估的良好生物标志物。生物标志物8-羟基-2'-脱氧鸟苷(8-OHdG)或8-氧代G已经成为测量内源性氧化损伤对DNA的影响的关键标志物,并且是致癌作用的起始和促进因素。生物标志物已被用于估计人类接触致癌因子后的DNA损伤,如烟草烟雾,石棉纤维,重金属和多环芳烃[1]。 |
| 参考文献 |
| 密度 | 2.3±0.1 g/cm3 |
|---|---|
| 熔点 | 217-220ºC |
| 分子式 | C10H13N5O5 |
| 分子量 | 283.241 |
| 精确质量 | 283.091675 |
| PSA | 159.51000 |
| LogP | -1.32 |
| InChIKey | HCAJQHYUCKICQH-VPENINKCSA-N |
| SMILES | Nc1nc2c([nH]c(=O)n2C2CC(O)C(CO)O2)c(=O)[nH]1 |
| 外观性状 | 白色固体 |
| 折射率 | 1.955 |
| 储存条件 | 2-8°C冷藏 |
| 分子结构 | 1、 摩尔折射率:60.81 2、 摩尔体积(m3/mol):125.4 3、 等张比容(90.2K):418.4 4、 表面张力(dyne/cm):123.8 5、 极化率(10-24cm3):24.10 |
| 计算化学 | 1、 疏水参数计算参考值(XlogP):-2.6 2、 氢键供体数量:5 3、 氢键受体数量:7 4、 可旋转化学键数量:2 5、 互变异构体数量:12 6、 拓扑分子极性表面积(TPSA):150 7、 重原子数量:20 8、 表面电荷:0 9、 复杂度:544 10、同位素原子数量:0 11、确定原子立构中心数量:3 12、不确定原子立构中心数量:0 13、确定化学键立构中心数量:0 14、不确定化学键立构中心数量:0 15、共价键单元数量:1 |
| 更多 | 1. 性状:未确定 2. 密度(g/mL25 ºC):未确定 3. 相对蒸汽密度(g/mL,空气=1):未确定 4. 熔点(ºC):217-220 5. 沸点(ºC,常压):未确定 6. 沸点(ºC2mmHg):未确定 7. 折射率:未确定 8. 闪点(ºC):未确定 9. 比旋光度(º):未确定 10. 自燃点或引燃温度(ºC):未确定 11. 蒸气压(Pa,):未确定 12. 饱和蒸气压(kPa,60ºC):未确定 13. 燃烧热(KJ/mol):未确定 14. 临界温度(ºC):未确定 15. 临界压力(KPa):未确定 16. 油水(正辛醇/水)分配系数的对数值:未确定 17. 爆炸上限(%,V/V):未确定 18. 爆炸下限(%,V/V):未确定 19. 溶解性:未确定 |
| 个人防护装备 | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| 安全声明 (欧洲) | 24/25 |
| 危险品运输编码 | NONH for all modes of transport |
| WGK德国 | 3 |
| RTECS号 | MF8782675 |
| 海关编码 | 2934999090 |
| 8-羟基-2-脱氧鸟苷上游产品 4 | |
|---|---|
| 8-羟基-2-脱氧鸟苷下游产品 0 | |
| 海关编码 | 2934999090 |
|---|---|
| 中文概述 | 2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0% |
| 申报要素 | 品名, 成分含量, 用途 |
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Complement-dependent NADPH oxidase enzyme activation in renal ischemia/reperfusion injury.
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Axitinib induces DNA damage response leading to senescence, mitotic catastrophe, and increased NK cell recognition in human renal carcinoma cells.
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Effect of long-term human exposure to environmental heavy metals on the expression of detoxification and DNA repair genes.
Environ. Pollut. 181 , 226-32, (2013) The present study was designed to evaluate the influence of long-term environmental human exposure to three heavy metals, lead (Pb), cadmium (Cd), and mercury (Hg), on the expression of detoxifying, x... |
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实验名称:Inhibitory activity against cellular differentiation in Friend erythroleukemia cells ...
来源:ChEMBL
靶标:Friend leukemia cell line
External Id:CHEMBL685365
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实验名称:Inhibitory activity against cellular differentiation in Friend erythroleukemia cells ...
来源:ChEMBL
靶标:Friend leukemia cell line
External Id:CHEMBL682042
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实验名称:Inhibitory activity against cellular replication in Friend erythroleukemia cells as g...
来源:ChEMBL
靶标:Friend leukemia cell line
External Id:CHEMBL682041
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实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
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实验名称:Firefly luciferase (FLuc-C-HiBiT) enzymatic inhibition screen - Functional assay
来源:NCGC
External Id:adst_SDR_Fluc-Fluc_Km
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实验名称:Experimentally measured binding affinity data (Kd) for protein-ligand complexes deriv...
来源:Shanghai Institute of Organic Chemistry
靶标:N/A
External Id:PDBbind-Kd for protein-ligand complexes
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实验名称:Firefly luciferase (FLuc-C-HiBiT) SDR gain of signal screen - plus ATP
来源:NCGC
External Id:adst_SDR_Fluc-HiBit_ATP
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实验名称:Firefly luciferase (FLuc-C-HiBiT) SDR gain of signal screen - without ATP
来源:NCGC
External Id:adst_SDR_Fluc-HiBit_NoATP
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实验名称:Cytotoxicity against mouse RAW264.7 cells assessed as cell viability after 48 hrs by ...
来源:ChEMBL
靶标:RAW264.7
External Id:CHEMBL3579568
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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| 2'-deoxy-7,8-dihydro-8-oxo-guanosine |
| MFCD00210311 |
| 2'-Deoxy-8-oxo-7,8-dihydroguanosine |
| 7,8-Dihydro-8-oxo-2'-deoxyguanosine |
| 2'-Deoxy-8-oxoguanosine |
| 8-Oxo-7,8-dihydrodeoxyguanosine |
| 2'-Deoxy-8-oxo-D-guanosine |
| 8-Oxodeoxyguanosine |
| 2'-Deoxy-8-hydroxyguanosine |
| 8-oxo-7,8-dihydro-2'-deoxiguanosine |
| 8-oxo-7-hydrodeoxyguanosine |
| 8-hydroxydeoxyguanosine |
| 8-HYDROXY-2'-DEOXYGUANOSINE |
| 8-Hydroxy-2’-deoxyguanosine |
| 8-oxo-7,8-dihydro-2'-deoxyguanosine |
| 2'-Deoxy-7,8-dihydro-8-oxoguanosine |