M9020
美加明 盐酸盐
≥98% (TLC), powder, nAChR antagonist
别名:
2-（甲氨基）异樟烷 盐酸盐, N,2,3,3-四甲基二环 [2.2.1] 庚烷-2-胺 盐酸盐, 盐酸美加明
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关于此项目
经验公式（希尔记法）:
C11H21N · HCl
化学文摘社编号:
分子量:
203.75
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
212-555-8
MDL number:
产品名称
美加明 盐酸盐,
InChI key
PKVZBNCYEICAQP-CIISUUNXSA-N
InChI
1S/C11H21N.ClH/c1-10(2)8-5-6-9(7-8)11(10,3)12-4;/h8-9,12H,5-7H2,1-4H3;1H/t8-,9+,11?;/m1./s1
SMILES string
Cl.[H][C@@]12CC[C@@]([H])(C1)C(C)(NC)C2(C)C
form
powder
solubility
ethanol: 122 mg/mL
H2O: 47 mg/mL
isopropanol: 476 mg/mL
glycerol: 95 mg/mL
originator
AstraZeneca
Quality Level
Gene Information
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相关类别
Application
在电流钳记录期间，美卡拉明盐酸盐已被用作细胞外盐水中的添加剂以减少突触输入。它还被用作主动脉体神经元和 MLO-Y4 细胞中的非选择性烟碱乙酰胆碱受体阻断剂。
Biochem/physiol Actions
非竞争性烟碱乙酰胆碱受体拮抗剂；优先阻断自主神经节的烟碱受体；穿过血脑屏障。
Disclaimer
溶液在高压灭菌时稳定。
Features and Benefits
该化合物在受体分类和信号转导手册的乙酰胆碱受体（烟碱型）页面上有详细描述。想要浏览手册的其他页面， 请单击此处。
该化合物由 AstraZeneca 公司开发。若要浏览其他制药公司研发的化合物和批准的药物/候选药物列表，请单击此处。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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In the present study the neuronal expression of Fos, the protein product of c-fos, was used to study changes in neuronal activity in nerve terminal regions of the ascending dopaminergic system during nicotine withdrawal. Rats were infused for 14 days
Acetylcholine affects osteocytic MLO-Y4 cells via acetylcholine receptors
Ma Y, et al.
Molecular and cellular endocrinology, 384(1-2), 155-164 (2014)
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The Journal of neuroscience : the official journal of the Society for Neuroscience, 19(21), 9180-9191 (1999-10-26)
The main olfactory bulb is a critical relay step between the olfactory epithelium and the olfactory cortex. A marked feature of the bulb is its massive innervation by cholinergic inputs from the basal forebrain. In this study, we addressed the
Potential roles of ATP and local neurons in the monitoring of blood O2 content by rat aortic bodies
Piskuric NA, et al.
Experimental Physiology, 99(1), 248-261 (2014)
M I Damaj et al.
The Journal of pharmacology and experimental therapeutics, 291(3), 1284-1291 (1999-11-24)
Pharmacological mechanisms involved in nicotine-induced seizures were investigated in mice by testing the ability of several nicotinic agonists in producing seizures after peripheral administration. In addition, nicotinic antagonists such as hexamethonium, mecamylamine, dihydro-beta-erythroidine, and methyllycaconitine citrate (MLA) were used in
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