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69014-14-8

中文名稱 硫替丁
英文名稱 TIOTIDINE
CAS 69014-14-8
分子式 C10H16N8S2
分子量 312.42
MOL 文件 69014-14-8.mol
69014-14-8 結(jié)構(gòu)式 69014-14-8 結(jié)構(gòu)式

基本信息

中文別名
硫替丁
英文別名
TIOTIDINE
ICI-125211
1-cyano-3-[2-[(2-guanidinothiazol-4-yl)methylthio]ethyl]-2-methyl-guanidine
1-Methyl-2-cyano-3-[2-[2-(diaminomethyleneamino)thiazole-4-ylmethylthio]ethyl]guanidine
1-Methyl-2-cyano-3-[2-[[2-(diaminomethyleneamino)thiazole-4-yl]methylthio]ethyl]guanidine
N-[2-[[[2-[(Aminoiminomethyl)amino]-4-thiazoyl]methyl]thio]ethyl]-N'-cyano-N''-methylguanidine
N'-Cyano-N-[2-[[[2-[(aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]ethyl]-N''-methylguanidine
N-[2-[[[2-[(Aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]ethyl]-N'-cyano-N''-methylguanidine
1-cyano-3-[2-[[2-(diaminomethylideneamino)-1,3-thiazol-4-yl]methylsulfanyl]ethyl]-2-methylguanidine
1-[2-[[2-[bis(azanyl)methylideneamino]-1,3-thiazol-4-yl]methylsulfanyl]ethyl]-3-cyano-2-methyl-guanidine

物理化學(xué)性質(zhì)

沸點(diǎn)490.1±55.0 °C(Predicted)
密度1.50±0.1 g/cm3(Predicted)
儲存條件Store at RT
溶解度Soluble to 10 mM in ethanol and to 100 mM in DMSO
酸度系數(shù)(pKa)pKa 6.80 (Uncertain)
形態(tài)粉末
顏色White to yellow
硫替丁價(jià)格(試劑級)
報(bào)價(jià)日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價(jià)格
2024/11/08HY-101232硫替丁
Tiotidine
69014-14-81mg545元
2024/11/08HY-101232硫替丁
Tiotidine
69014-14-85mg1200元
2024/11/08HY-101232硫替丁
Tiotidine
69014-14-810mM * 1mLin DMSO1320元

常見問題列表

生物活性
Tiotidine (ICI 125211) 是一種有效選擇性 H2 受體 (histamine H2-receptor) 拮抗劑 (pA2=7.3-7.8)。Tiotidine (ICI 125211) 對 H1 和 H3 受體均具有低親和力。
靶點(diǎn)

H 2 Receptor

7.3-7.8 (pA2)

H 3 Receptor

4.8 (pA2)

體外研究

Tiotidine competitively antagonizes the positive chronotropic action of histamine with an apparent dissociation constant of 30 μM (23-38 μM). Tiotidine abolishes H2-mediated increases in contractile force leaving H2-mediated negative inotropic responses unopposed. The actions of histamine at the A-V node, manifested by lengthening of the P-R interval and A-V block, are attenuated by 2.5 x 10(-7) M Tiotidine.
Tiotidine actually behaves as an inverse agonist in U-937 cells, diminishing basal cAMP levels.

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