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51116-01-9

中文名稱 8-溴代鳥苷-3',5'-環(huán)狀單磷酸酯鈉鹽
英文名稱 8-BROMOGUANOSINE 3',5'-(CYCLIC) MONOPHOSPHATESODIUM SALT N-HYDRATE
CAS 51116-01-9
分子式 C10H10BrN5O7P.Na
分子量 446.08
MOL 文件 51116-01-9.mol
51116-01-9 結(jié)構(gòu)式 51116-01-9 結(jié)構(gòu)式

基本信息

中文別名
8-溴代鳥苷-3',5'-環(huán)狀單磷酸酯鈉鹽
英文別名
BR-CGMP, NA
8-BR-CGMP NA
8-BROMO-CGMP NA
Einecs 256-993-8
8-BROMO-CGMP SODIUM
8-BR-CGMP SODIUM SALT
(115974-70-4) 8-AET-cGMP
8-BROMO-CGMP, SODIUM SALT
8-bromo-Cyclic GMP (sodium salt)
8-BROMOGUANOSINE-3',5'-CYCLOPHOSPHATE SODIUM

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C
溶解度H2O: 100 mg/mL
溶解度H2O:100 mg/mL
形態(tài)powder
顏色White to off-white
水溶解性溶于水至100mM

安全數(shù)據(jù)

WGK Germany3
WGK Germany3
海關(guān)編碼29349990
8-溴代鳥苷-3',5'-環(huán)狀單磷酸酯鈉鹽價(jià)格(試劑級)
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
2024/11/08HY-101379A8-溴代鳥苷-3',5'-環(huán)狀單磷酸酯鈉鹽
8-Bromo-cGMP sodium
51116-01-95mg700元
2024/11/08HY-101379A8-溴代鳥苷-3',5'-環(huán)狀單磷酸酯鈉鹽
8-Bromo-cGMP sodium
51116-01-910mM * 1mLin Water770元
2024/11/08HY-101379A8-溴代鳥苷-3',5'-環(huán)狀單磷酸酯鈉鹽
8-Bromo-cGMP sodium
51116-01-910mg1100元

常見問題列表

生物活性
8-Bromo-cGMP sodium 是 cGMP 的膜滲透性類似物,是一種 PKG 激活劑。8-Bromo-cGMP sodium 可顯著抑制 Ca2+ 宏觀電流并損害高 K+ 刺激的胰島素釋放。8-Bromo-cGMP sodium 具有鎮(zhèn)痛和血管舒張作用。
靶點(diǎn)

Ca 2+

體外研究

8-Bromo-cGMP sodium (1-100 μM; 8 h) increases resistance of LLC-PK1 cells to CsA toxicity concentration-dependently.
8-Bromo-cGMP sodium (1-100 μM; 16 h) induces the synthesis of HO-1 protein in a concentration-dependent fashion.

Cell Viability Assay

Cell Line: LLC-PK1 cells (ATCC CL 101)
Concentration: 1-100 μM
Incubation Time: 8 hours
Result: Increased resistance of LLC-PK1 cells to Cyclosporin A (CsA) toxicity concentration-dependently and augmented cell viability by up to 65%.

Western Blot Analysis

Cell Line: LLC-PK1 cells (ATCC CL 101)
Concentration: 1-100 μM
Incubation Time: 16 hours
Result: Induced the synthesis of HO-1 protein in a concentration-dependent fashion.
體內(nèi)研究

8-Bromo-cGMP sodium (0.3, 1, 3.0 nmol; intrathecal administration; 10 min before test) dose-dependently and significantly increases the tail-flick latency in Vincristine-treated mice to the level observed in vehicle-treated naive mice (male ICR mice, 4weeks of age and weighing 20 g). Vincristine (0.05 mg/kg 1 day after the pre-drug tail-flick latency, and then 0.125 mg/kg twice a week for 6 weeks) can induce painful neuropathy in mice.
8-Bromo-cGMP sodium (10 mg/kg; iv; single dose) results in vasodilator responses in eNOS-Tg mice and WT littermates in C57BL/6 background (19-35 g).

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