货号:A204150
同义名:
2',3'-二脱氧腺苷
/ 2′,3′-Dideoxyadenosine; ddA
2',3'-Dideoxyadenosine是脱氧腺苷的核苷类似物。它抑制腺苷酸环化酶,可能在抑制肿瘤进展中发挥关键作用。它是 HIV 逆转录酶的强效抑制剂。


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| Concentration | Treated Time | Description | References | |
| HeLa cells | 0.1-50 µM | 4 days | Inhibited T. cruzi growth, with effects similar to ddI | Antimicrob Agents Chemother. 1996 Nov;40(11):2455-8 |
| rat brain astrocytes | 20 μM | 15 min | Investigate the mechanism of DHA and AA release under ATP stimulation, finding that DDA (2',3'-Dideoxyadenosine) almost completely blocks ATP-induced AA release. | Br J Pharmacol. 2003 Jul;139(5):1014-22 |
| Human bronchial epithelial cells (16HBE14o- cell line) | 200 µM | Inhibited adenylate cyclase activity, thereby completely abolishing the aldosterone-induced [Ca2+]i decrease | J Physiol. 2001 Nov 15;537(Pt 1):267-75 | |
| Guinea-pig thalamic slice relay neurones of the dorsal lateral geniculate nucleus (LGND) | 50-100 μM | 2',3'-Dideoxyadenosine mimicked the decrease in Ih evoked by A1 receptor activation through inhibition of adenylyl cyclase activity. | J Physiol. 1992 Feb;447:729-53 | |
| Rat ventral tegmental area neurons | 100 μM | 2',3'-Dideoxyadenosine, an adenylyl cyclase inhibitor, was used to study its effect on Ih current. Results showed that 2',3'-dideoxyadenosine did not affect Ih current nor alter dopamine's inhibition of Ih. | J Physiol. 1993 Mar;462:753-64 | |
| TM3 cells | 100 μM | 20 days | Protect cells from viral infection and maintain their immune reactivity. | Proc Natl Acad Sci U S A. 1987 Apr;84(7):2033-7 |
| ATH8 cells | 50 μM | 30 days | Inhibit HTLV-III/LAV DNA synthesis and mRNA expression, protecting cells from viral infection. | Proc Natl Acad Sci U S A. 1987 Apr;84(7):2033-7 |
| Administration | Dosage | Frequency | Description | References | ||
| Swiss albino mice | Systemic infection model | Oral or subcutaneous | 12 to 219 mg/kg | Treatment immediately, 5, 24, 29, 48, and 72 hours post-infection, observed for 14 days | Evaluate the antibacterial activity of DDA in a mouse systemic infection model, showing protective effects against multiple strains at doses well below toxic levels. | Antimicrob Agents Chemother. 1981 Mar;19(3):424-8. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
4.25mL 0.85mL 0.43mL |
21.25mL 4.25mL 2.13mL |
42.51mL 8.50mL 4.25mL |
|
| CAS号 | 4097-22-7 |
| 分子式 | C10H13N5O2 |
| 分子量 | 235.24 |
| SMILES Code | OC[C@H]1O[C@@H](N2C=NC3=C(N)N=CN=C23)CC1 |
| MDL No. | MFCD00010534 |
| 别名 | 2',3'-二脱氧腺苷 ;2′,3′-Dideoxyadenosine; ddA; D2A; CCRIS 428; Dideoxyadenosine; NSC 98700; ddAdo |
| 运输 | 蓝冰 |
| InChI Key | WVXRAFOPTSTNLL-NKWVEPMBSA-N |
| Pubchem ID | 20039 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 105 mg/mL(446.35 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 100 mg/mL(425.09 mM),配合低频超声助溶 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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