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127910-31-0

中文名稱 (E)-(±)-2-AMINO-4-METHYL-5-PHOSPHONO-3-PENTENOIC ACID
英文名稱 (E)-(+/-)-2-AMINO-4-METHYL-5-PHOSPHONO-3-PENTENOIC ACID
CAS 127910-31-0
分子式 C6H12NO5P
分子量 209.14
MOL 文件 127910-31-0.mol
127910-31-0 結(jié)構(gòu)式 127910-31-0 結(jié)構(gòu)式

基本信息

中文別名
(E)-2-氨基-4-甲基-5-膦酰基-3-戊烯酸
英文別名
CGP 37849
CGP 37849
CGP-37849
CGP37849
dl-2-amino-4-methyl-5-phosphono-3-*pentenoic acid
(E)-2-Amino-4-methyl-5-phosphonopent-3-enoic acid
(3E)-2-Amino-4-methyl-5-phosphono-3-pentanoic acid
(E)-(±)-2-AMINO-4-METHYL-5-PHOSPHONO-3-PENTENOIC ACID
3-Pentenoic acid, 2-amino-4-methyl-5-phosphono-, (3E)-
(E)-(+/-)-2-AMINO-4-METHYL-5-PHOSPHONO-3-PENTENOIC ACID

物理化學(xué)性質(zhì)

沸點(diǎn)523.1±60.0 °C(Predicted)
密度1.506±0.06 g/cm3(Predicted)
儲(chǔ)存條件Desiccate at +4°C
溶解度在水中的溶解度為≥2mg/mL(加熱)
酸度系數(shù)(pKa)1.83±0.10(Predicted)
形態(tài)粉末
顏色白色至米色
水溶解性H2O: 100mM

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)有害 (GHS07)
GHS07
警示詞警告
危險(xiǎn)性描述H315-H319-H335
危險(xiǎn)品標(biāo)志Xi
危險(xiǎn)類別碼36/37/38
安全說明26-36
WGK Germany3
(E)-(±)-2-AMINO-4-METHYL-5-PHOSPHONO-3-PENTENOIC ACID價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2026/06/05HY-107702(E)-(±)-2-AMINO-4-METHYL-5-PHOSPHONO-3-PENTENOIC ACID
CGP 37849
127910-31-01mg1550元
2026/06/05HY-107702(E)-(±)-2-AMINO-4-METHYL-5-PHOSPHONO-3-PENTENOIC ACID
CGP 37849
127910-31-05mg3850元
2026/06/05HY-107702(E)-(±)-2-AMINO-4-METHYL-5-PHOSPHONO-3-PENTENOIC ACID
CGP 37849
127910-31-010 mg5550元

常見問題列表

生物活性
CGP 37849 是一種有效的競爭性口服活性 N-甲基-D-天冬氨酸 (NMDA) 受體拮抗劑。CGP 37849 是嚙齒動(dòng)物的抗驚厥藥,具有抗抑郁和抗焦慮作用。
體外研究

In the hippocampal slice in vitro, CGP 37849 selectively and reversibly antagonizes NMDA-evoked increases in CA1 pyramidal cell firing rate. In slices bathed in medium containing low Mg 2+ levels, concentrations of CGP 37849 up to 10 μM suppresses burst firing evoked in CA1 neurones by stimulation of Schaffer collateral-commissural fibres without affecting the magnitude of the initial population spike.

體內(nèi)研究

CGP 37849 potently ( K i of 220 nM) and competitively inhibits NMDA-sensitive l-[ 3 H]-glutamate binding to postsynaptic density (PSD) fractins from rat brain. CGP 37849 inhibits the binding of the selective NMDA receptor antagonist, [ 3 H]-(±)-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonate (CPP), with a K i of 35 nM.
In vivo, oral administration to rats of CGP 37849 selectively blocks firing in hippocampal neurones induced by ionophoretically-applied NMDA, without affecting the responses to quisqualate or kainate.
Oral administration to mice of CGP 37849 suppresses maximal electroshock-induced seizures in mice with an ED 50 of 21 mg/kg.

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