129-46-4
129-46-4 結(jié)構(gòu)式
基本信息
蘇拉明鈉
舒拉明鈉
蘇拉明
蘇拉明鈉
8,8'-[CARBONYLBIS[IMINO-3,1-PHENYLENECARBONYLIMINO(4-METHYL-3,1-PHENYLENE)CARBONYLIMINO]]BIS-1,3,5-NAPHTHALENETRISULFONIC ACID HEXASODIUM SALT
8,8'-CARBONYLBIS[IMINO-3,1-PHENYLENECARBONYLIMINO(4-METHYL-3,1-PHENYLENE)CARBONYLIMINO]BIS-1,3,5-NAPHTHALENETRISULFONIC ACID HEXASODIUM
8,8'-carbonylbisimino-3,1-phenylenecarbonylimino-(4-methyl-3,1-phenylene)carbonyliminobis-1,3,5-naphthalenetrisulfonic acid hexasodium
SURAMINE SODIUM SALT
SURAMIN HEXASODIUM SALT
SURAMIN SODIUM
SURAMIN SODIUM SALT
1-(3-benzamido-4-methylbenzamido)naphthalene-4,6,8-trisulfonicacidsym-3’’-u
1,3,5-naphthylenetrisulfonicacid,8,8’-(ureylenebis(m-phenylenecarbonylimino(4
309f
antrypol
bay205
bayer205
fourneau309
germanin
moranyl
naganin
naganine
naphuridesodium
物理化學(xué)性質(zhì)
安全數(shù)據(jù)
常見(jiàn)問(wèn)題列表
蘇拉明鈉是一種可逆的競(jìng)爭(zhēng)性蛋白酪氨酸磷酸酶 (PTPases) 抑制劑。蘇拉明鈉是有效的 sirtuins 抑制劑：SirT1 (IC50=297 nM)，SirT2 (IC50=1.15 μM)，SirT5 (IC50=22 μM)。蘇拉明鈉是競(jìng)爭(zhēng)性逆轉(zhuǎn)錄酶抑制劑 (DNA topoisomerase II: IC50=5 μM)。蘇拉明鈉有效抑制 IP5K，并且是抗寄生蟲(chóng) (antiparasitic)，抗腫瘤和抗血管生成劑。
蘇拉明鈉已經(jīng)被證實(shí)具有抗錐蟲(chóng)病，抗腫瘤，防治眼部增殖性疾病，抗病毒，免疫調(diào)節(jié)劑的作用，并廣泛應(yīng)用于臨床實(shí)踐中。目前尚未有蘇拉明鈉具有抗雞球蟲(chóng)作用的報(bào)導(dǎo)，通過(guò)蘇拉明鈉已知的性質(zhì)無(wú)法推斷其是否具有抗雞球蟲(chóng)的作用。
蘇拉明鈉鹽，是一種丙型肝炎病毒 NS3 解旋酶抑制劑。 也用于治療因膠原蛋白問(wèn)題引起的關(guān)節(jié)炎。
|
SIRT1 297 nM (IC 50 ) |
SIRT2 1.15 μM (IC 50 ) |
SIRT5 22 μM (IC 50 ) |
Suramin sodium salt (Suramin hexasodium salt; 50-600 μg/mL; for 24-96 hours) inhibits cells proliferation in a dose-dependent and time-dependent manner and decreases viability in cancer cells.
Suramin sodium salt (300 μg/mL; for 48 hours) induces cells apoptosis and down-regulates mRNA expression in HeLa cells.
Suramin sodium salt (1 mg/mL; 1 hour) significantly suppresses the phosphorylated ERK1/2.
The IC
50
values of HO-8910 PM and HeLa are 319 μg/mL, 476 μg/mL, respectively.
Suramin blocks viral replication in Vero E6 cells.
Cell Proliferation Assay
| Cell Line: | HO-8910 PM ovarian and Hela cervical cancer cells |
| Concentration: | 50, 100, 200, 300, 400, 500 and 600 μg/mL |
| Incubation Time: | For 24, 48, 72 and 96 hours |
| Result: | Inhibited cells proliferation in a dose-dependent and time-dependent manner. |
Apoptosis Analysis
| Cell Line: | HeLa cells |
| Concentration: | 300 μg/mL |
| Incubation Time: | For 48 hours |
| Result: | Induced cells apoptosis. |
Western Blot Analysis
| Cell Line: | PA-SMCs cells |
| Concentration: | 1 mg/mL |
| Incubation Time: | For 1 hour |
| Result: | Significantly suppressed the phosphorylated ERK1/2. |
Suramin sodium salt (Suramin hexasodium salt; 10 mg/kg; IV; twice weekly for 3 weeks) reverses established pulmonary hypertension (PH), thereby normalizing the pulmonary artery pressure values and vessel structure.
| Animal Model: | Adult male Wistar rats (200-225 g) |
| Dosage: | 10 mg/kg |
| Administration: | IV; twice weekly for 3 weeks |
| Result: | Reversed established PH, thereby normalizing the pulmonary artery pressure values and vessel structure. |