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151837-09-1

中文名稱 ADENOSINE 3',5'-CYCLIC MONOPHOSPHOROTHIOATE, RP-ISOMER, TRIETHYLAMMONIUM SALT
英文名稱 ADENOSINE 3',5'-CYCLIC MONOPHOSPHOROTHIOATE, RP-ISOMER, TRIETHYLAMMONIUM SALT
CAS 151837-09-1
分子式 C16H27N6O5PS
分子量 446.46
MOL 文件 151837-09-1.mol
151837-09-1 結(jié)構(gòu)式 151837-09-1 結(jié)構(gòu)式

基本信息

中文別名
(R)-腺苷 環(huán)3',5'-(硫代磷酸氫酯)三乙胺鹽
英文別名
RP-CAMPS TEA
CAMPS TEA, RP-ISOMER
OXIPZMKSNMRTIV-RNSTXJOVSA-N
RP-CAMPS TRIETHYL AMMONIUM SALT
CAMPS-RP, TRIETHYLAMMONIUM SALT
rp-camps triethylammonium salt hydrate
Rp-Cyclic AMPS (triethylammonium salt)
ADENOSINE 3',5'-CYCLIC PHOSPHOROTHIOATE-RP, TRIETHYLAMMONIUM SALT
Rp-Adenosine 3′,5′-cyclic monophosphorothioate triethylammonium salt
Rp-Cyclic 3′,5′-hydrogen phosphorothioate adenosine triethylammonium salt

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C
溶解度H2O:可溶,10mg/mL
形態(tài)粉末
顏色白色至米色
水溶解性溶于水至100mM
最大波長(zhǎng)(λmax)258 nm
InChIKeyOXIPZMKSNMRTIV-NVGWRVNNSA-N
SMILESCCN(CC)CC.Nc1ncnc2n(cnc12)[C@@H]3O[C@@H]4COP(O)(=S)O[C@H]4[C@H]3O

安全數(shù)據(jù)

WGK Germany3
存儲(chǔ)類別11 - Combustible Solids
ADENOSINE 3',5'-CYCLIC MONOPHOSPHOROTHIOATE, RP-ISOMER, TRIETHYLAMMONIUM SALT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
2025/12/22HY-100530ADENOSINE 3',5'-CYCLIC MONOPHOSPHOROTHIOATE, RP-ISOMER, TRIETHYLAMMONIUM SALT
Rp-cAMPS triethylammonium salt
151837-09-11mg6750元

常見(jiàn)問(wèn)題列表

生物活性
Rp-cAMPS triethylammonium salt,一種 cAMP 的類似物,是一種 cAMP 誘導(dǎo)的 PKA I 和 PKA II 活化 (Ki 分別為 12.5 μM 和 4.5 μM) 的有效的,競(jìng)爭(zhēng)性拮抗劑。Rp-cAMPS triethylammonium salt 耐磷酸二酯酶水解。
靶點(diǎn)

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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