您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > A134974
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
A134974
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
A134974图片
CAS NO:186141-75-3
规格:≥98%
包装与价格:
包装价格(元)
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW) 375.17
Formula C11H14IN5O2
CAS No. 186141-75-3
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 10 mM
Water: N/A
Ethanol: N/A
Other info

Chemical Name: (1S,2R,3S,5R)-3-amino-5-{4-amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl}cyclopentane-1,2-diol

InChi Key: NSXJHIFQIZKLGF-LWIVVEGESA-N

InChi Code: InChI=1S/C11H14IN5O2/c12-4-2-17(6-1-5(13)8(18)9(6)19)11-7(4)10(14)15-3-16-11/h2-3,5-6,8-9,18-19H,1,13H2,(H2,14,15,16)/t5-,6+,8+,9-/m0/s1

SMILES Code: O[C@@H]1[C@H](O)[C@@H](N)C[C@H]1N2C=C(I)C3=C(N)N=CN=C32

SynonymsA134974; A 134974; A-134974
实验参考方法
In Vitro

In vitro activity: AK enzyme inhibition was assayed radiochemically as described byYamada et al. (1980) and McNally et al. (1997). The ability of A-134974 to inhibit AK activity in intact IMR-32 neuroblastoma cells (American Type Culture Collection, Gaithersburg, MD) carried out as previously described (Kowaluk and Cowart, 1994). Radioligand binding assay methodology for the A1, A2A, and A3 receptors was carried out as described by Jarvis et al. (2000). The ability of A-134974 to inhibit [3H]nitrobenzylthioinosine binding to the ADO transporter and to inhibit adenosine deaminase activity was also examined using previously described methodology (Parkinson and Geiger, 1996).

In VivoDrugs administered to rats were A-134974 (Cowart, 1997, an AK inhibitor synthesized at Abbott Laboratories), morphine sulfate (Mallinckrodt, St. Louis, MO), and theophylline (a nonselective ADO receptor antagonist; Sigma Chemical Co., St. Louis, MO). All drugs were dissolved in sterile water for local (intraplantar, i.t., or i.c.v.) or systemic (i.p.) delivery. The drug administration procedures described below were followed for locomotor activity experiments as well as for hyperalgesia experiments. Each experimental group consisted of at least five animals.
Animal model Male Sprague-Dawley rats (260–320 g)
Formulation & DosageSystemic Administration of A-134974: A-134974 (0.3–30 μmol/kg) or vehicle was administered i.p. 30 min before testing.
Local Administration of A-134974: A-134974 (3–100 nmol) or vehicle was injected directly into 1) the lumbar spinal cord via indwelling intrathecal catheters, 2) the right lateral ventricle, or 3) the intraplantar region of a carrageenan-inflamed hindpaw (hyperalgesia experiments only).
References J Pharmacol Exp Ther. 2001 Feb;296(2):501-9.