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73208-40-9

英文名稱 SP-ADENOSINE 3',5'-CYCLIC MONOPHOSPHOTHIOATE TRIETHYLAMINE
CAS 73208-40-9
分子式 C16H27N6O5PS
分子量 446.46
MOL 文件 73208-40-9.mol
73208-40-9 結(jié)構(gòu)式 73208-40-9 結(jié)構(gòu)式

基本信息

英文別名
SP-CAMPS TEA
(R)-Adenosine
CAMPS TEA, SP-ISOMER
cAMPS-Rp, triethylam
SP-CAMPS TRIETHYLAMINE
RP-CAMPS TRIETHYLAMINE
SP-CAMPS TRIETHYL AMMONIUM SALT
CAMPS-SP, TRIETHYLAMMONIUM SALT
Cyclic3',5'-(hydrogenphosphorothioate)triethylammonium
SP-ADENOSINE 3',5'-CYCLIC MONOPHOSPHOTHIOATE TRIETHYLAMINE

物理化學性質(zhì)

儲存條件−20°C
溶解度H2O: soluble
形態(tài)solid
顏色white

安全數(shù)據(jù)

安全說明22-24/25
WGK Germany3

常見問題列表

生物活性
Rp-cAMPS,一種 cAMP 的類似物,是一種 cAMP 誘導的 PKA I 和 PKA II 活化 (Ki 分別為 12.5 μM 和 4.5 μM) 的有效的,競爭性拮抗劑。Rp-cAMPS 耐磷酸二酯酶水解。
靶點

Ki: 6.05 μM (PKA I) and 9.75 μM (PKA II)

體外研究

A membrane-permeable competitive cAMP antagonist (Rp-cAMPS) that blocks PKA activation by binding to the regulatory subunits without dissociating the kinase holoenzyme also inhibits synaptic plasticity but has no effect on normal synaptic transmission.

體內(nèi)研究

Rp-cAMPS (10 μM, 15 min) decreases the monosynaptic EPSCs evoked at the PB-CeLC and BLA-CeLC synapses in slices from arthritic rats but not in control neurons from normal animals. The inhibitory effect of Rp-cAMPS is significant compared to predrug (ACSF) control values obtained in the same neurons.

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