1-Adamantanamine HCl

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Chemical Structure| 665-66-7 同义名 : 盐酸金刚烷胺 ;1-Aminoadamantane hydrochloride; 1-Adamantylamine hydrochloride; NSC 83653; Aminoadamantane; Adamantylamine; Amantadine (hydrochloride); Amantadine HCl; 1-Adamantanamine hydrochloride; Amantadine hydrochloride
CAS号 : 665-66-7
货号 : A183434
分子式 : C10H18ClN
纯度 : 98%
分子量 : 187.71
MDL号 : MFCD00074723
存储条件:

Pure form Inert atmosphere, room temperature

In solvent -20°C:3-6个月-80°C:12个月

溶解度 : -
动物实验配方:
生物活性
描述 1-Adamantanamine Hydrochloride (amantadine hydrochloride), as a pro-dopaminergic drug and as an N-methyl-D-aspartate antagonist, makes amantadine an interesting candidate to improve consciousness and responsiveness in individuals with DOC (disorders of consciousness), including vegetative state and minimally conscious state[3]. 1-Adamantanamine hydrochloride (aminoadamantane) has been shown to inhibit the multiplication of influenza A viruses in cell cultures, organ cultures and experimentally infected mice. In a double-blind, placebo-controlled investigation of aminoadamantane given prophylactically, in doses of 100 mg every 12 hours for 10 days, no protective effect of the drug was demonstrated[4]. I-Adamantanamine hydrochloride, added to chick embryo cells, inhibited focus production upon subsequent inoculation of the cells with Rous and Esh sarcoma viruses. 1-adamantanamine hydrochloride are capable of supporting viral replication, the drug inhibits growth of two oncogenic viruses by prevention of virus penetration, but not by a virucidal effect or cell intoxication[5].
临床研究
NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT00513292 HER2/Neu Positive ... 展开 >> Stage IA Breast Cancer Stage IB Breast Cancer Stage II Breast Cancer Stage IIIA Breast Cancer 收起 << Phase 3 Unknown - -
NCT01441986 Type 2 Diabetes Mellitus Phase 2 Completed - Germany ... 展开 >> Profil Institute for Metabolic Research Neuss, NRW, Germany, 41460 收起 <<
NCT00513292 - Unknown - -
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

5.33mL

1.07mL

0.53mL

26.64mL

5.33mL

2.66mL

53.27mL

10.65mL

5.33mL

参考文献

[1]Salom, D., Hill BR, et al., pH-dependent tetramerization and amantadine binding of the transmembrane helix of M2 from the influenza A virus. Biochemistry, 2000. 39(46): p. 14160-70.

[2]Salom, D., Hill BR, et al., pH-dependent tetramerization and amantadine binding of the transmembrane helix of M2 from the influenza A virus. Biochemistry, 2000. 39(46): p. 14160-70.

[3]Formisano R, Zasler ND. Posttraumatic parkinsonism. J Head Trauma Rehabil. 2014;29(4):387‐390

[4]Galbraith AW, Oxford JS, Schild GC, Watson GI. Study of 1-adamantanamine hydrochloride used prophylactically during the Hong Kong influenza epidemic in the family environment. Bull World Health Organ. 1969;41(3):677‐682

[5]Wallbank AM, Matter RE, Klinikowski NG. 1-Adamantanamine hydrochloride: inhibition of Rous and Esh Sarcoma viruses in cell culture. Science. 1966;152(3730):1760‐1761