183364-82-1
183364-82-1 結(jié)構(gòu)式
基本信息
中文別名
化合物 T10880 英文別名
CPPGrac-CPPG
(RS)-CPPG
(RS)-α-Cyclopropyl-4-phosphonophenylglycine
(RS)-ALPHA-CYCLOPROPYL-4-PHOSPHONOPHENYLGLYCINE
(+/-)-ALPHA-CYCLOPROPYL-4-PHOSPHONOPHENYLGLYCINE
Benzeneacetic acid, α-amino-α-cyclopropyl-4-phosphono-
安全數(shù)據(jù)
警示詞警告
危險(xiǎn)性描述H302
防范說(shuō)明P264-P270-P301+P312-P330-P501
危險(xiǎn)品標(biāo)志Xn
危險(xiǎn)類(lèi)別碼22
WGK Germany3
CPPG價(jià)格(試劑級(jí))
報(bào)價(jià)日期 | 產(chǎn)品編號(hào) | 產(chǎn)品名稱(chēng) | CAS號(hào) | 包裝 | 價(jià)格 |
2025/02/05 | HY-101333 | CPPG | 183364-82-1 | 1 mg | 990元 |
2025/02/05 | HY-101333 | CPPG | 183364-82-1 | 5 mg | 2610元 |
常見(jiàn)問(wèn)題列表
生物活性
CPPG ((RS)-CPPG) 是一種有效的 II/III 型 mGlu 受體拮抗劑。CPPG 對(duì)大鼠大腦皮層中的 III 組 (IC50=2.2 nM) 比對(duì) II 組((IC50=46.2 nM) mGlu 受體有一定的選擇性 (約 20 倍)。CPPG 對(duì) I 組 mGlu 受體的作用較弱。靶點(diǎn)
group III mGlu receptors 2.2 nM (IC 50 ) |
group II mGlu receptors 46.2 nM (IC 50 ) |
體外研究
CPPG ((RS)-CPPG) potently reversed both L-AP4 (IC 50 =2.2 nM)- and L-CCG-I (IC 50 =46.2 nM) -mediated inhibition of forskolin-stimulated cyclic AMP accumulation in adult rat cortical slices. CPPG is a potent antagonist against group II/III mGlu receptors in the adult rat cortex and shows moderate selectivity for group III mGlu receptors. Conversely, CPPG has weak effects at group I mGlu receptors in both the neonatal rat cortex and cultured cerebellar granule cells.