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About This Item
线性分子式:
NH2(CH2)3COOH
CAS号:
分子量:
103.12
Beilstein:
906818
EC 号:
MDL编号:
UNSPSC代码:
12352103
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方案
97%
mp
195 °C (dec.) (lit.)
SMILES字符串
NCCCC(O)=O
InChI
1S/C4H9NO2/c5-3-1-2-4(6)7/h1-3,5H2,(H,6,7)
InChI key
BTCSSZJGUNDROE-UHFFFAOYSA-N
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应用
重要的抑制性神经递质。与异硫氰酸酯反应可生成具有抗真菌活性的硫脲。
生化/生理作用
大脑中的主要抑制性神经递质；GABAA 和 GABAB 受体激动剂；增加 Cl− 的传导性。
替代产品
产品编号
说明
价格
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Chem. Abstr., 120, 225805w-225805w (1994)
E Roberts et al.
Neurochemical research, 18(4), 365-376 (1993-04-01)
Alone of the known neurotransmitters, GABA is an electroneutral zwitterion (pI = 7.3) at physiological pH. This confers the highest probability of successfully traversing densely packed synaptic gaps without interacting electrostatically with charged entities enroute, making GABA a high fidelity
European Journal of Medicinal Chemistry, 26, 723-723 (1991)
Abraham Nudelman et al.
Journal of medicinal chemistry, 51(9), 2858-2862 (2008-03-28)
The perphenazine and fluphenazine GABA esters 3 and 4 evaluated in rat models for antipsychotic activity displayed a significant decrease of catalepsy associated with increased prolactin blood levels. Efficacy was evaluated in the d-amphetamine-induced hyperactivity model, where perphenazine abolished hyperactivity
Michaela Jansen et al.
Journal of medicinal chemistry, 51(15), 4430-4448 (2008-07-25)
Drugs used to treat various disorders target GABA A receptors. To develop alpha subunit selective compounds, we synthesized 5-(4-piperidyl)-3-isoxazolol (4-PIOL) derivatives. The 3-isoxazolol moiety was substituted by 1,3,5-oxadiazol-2-one, 1,3,5-oxadiazol-2-thione, and substituted 1,2,4-triazol-3-ol heterocycles with modifications to the basic piperidine substituent
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