Imiquimod-d9
						    			         
			    					
		(Synonyms: R 837-d9)		目录号 : GC47453
	A neuropeptide with diverse biological activities
     
    
Cas No.:2712126-48-0
Sample solution is provided at 25 µL, 10mM.
Imiquimod-d9 is intended for use as an internal standard for the quantification of imiquimod by GC- or LC-MS. Imiquimod is an imidazoquinoline agonist of toll-like receptor 7 (TLR7; EC50 = 2.12 μM).1 It increases TNF-α and IL-12 p40 production in IFN-γ-treated murine peritoneal macrophages in a concentration- and MyD88-dependent manner.2 Topical application of imiquimod (30 μl of 5% cream) increases TNF and IFN levels at the application site in hairless mice.3 Imiquimod dose-dependently increases serum levels of IFN-α in mice when administered by gavage.4 It reduces tumor growth in an MC-26 model of murine colon cancer when administered at a dose of 30 mg/kg every three days. Imiquimod (5 mg/kg, intravaginally, twice daily) reduces vaginal viral titer and lesion formation in a guinea pig model of genital HSV-2 infection.5 Formulations containing imiquimod have been used in the treatment of actinic keratosis, superficial basal cell carcinoma, and external genital warts.
1.Shukla, N.M., Mallardi, S.S., Mutz, C.A., et al.Structure-activity relationships in human toll-like receptor 7-active imidazoquinoline analoguesJ. Med. Chem.53(11)4450-4465(2010) 2.Hemmi, H., Kaisho, T., Takeuchi, O., et al.Small anti-viral compounds activate immune cells via the TLR7 MyD88-dependent signaling pathwayNat. Immunol.3(2)196-200(2002) 3.Imbertson, L.M., Beaurline, J.M., Couture, A.M., et al.Cytokine induction in hairless mouse and rat skin after topical application of the immune response modifiers imiquimod and S-28463J. Invest. Dermatol.110(5)734-739(1998) 4.Sidky, Y.A., Borden, E.C., Weeks, C.E., et al.Inhibition of murine tumor growth by an interferon-inducing imidazoquinolinamineCancer Res.52(13)3528-3533(1992) 5.Harrison, C.J., Jenski, L.J., Voychehovski, T., et al.Modification of immunological responses and clinical disease during topical R-837 treatment of genital HSV-2 infectionAntiviral Res.10(4-5)209-223(1988)
| Cas No. | 2712126-48-0 | SDF | |
| 别名 | R 837-d9 | ||
| Canonical SMILES | NC1=NC2=C(C3=C1N=CN3C([2H])([2H])C(C([2H])([2H])[2H])([2H])C([2H])([2H])[2H])C=CC=C2 | ||
| 分子式 | C14H7D9N4 | 分子量 | 249.4 | 
| 溶解度 | DMF: 1 mg/ml,DMSO: 1 mg/ml | 储存条件 | Store at -20°C | 
| General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 | ||
| Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
|  | 1 mg | 5 mg | 10 mg | 
| 1 mM | 4.0096 mL | 20.0481 mL | 40.0962 mL | 
| 5 mM | 801.9 μL | 4.0096 mL | 8.0192 mL | 
| 10 mM | 401 μL | 2.0048 mL | 4.0096 mL | 
| 第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
| 给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
| 第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
			           2.
			一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
			           3. 以上所有助溶剂都可在 GlpBio 网站选购。
			
Quality Control & SDS
- View current batch:
- Purity: >99.00% 
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
 
 
   
   
   
  














