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104961-19-5

中文名稱 104961-19-5
英文名稱 1H-Indole-2-carboxamide, 5-methoxy-3-(1-methylethoxy)-1-phenyl-N-2H-tetrazol-5-yl-
CAS 104961-19-5
分子式 C20H20N6O3
分子量 392.41
MOL 文件 104961-19-5.mol
104961-19-5 結(jié)構(gòu)式 104961-19-5 結(jié)構(gòu)式

基本信息

中文別名
化合物 T10054
英文別名
1H-Indole-2-carboxamide, 5-methoxy-3-(1-methylethoxy)-1-phenyl-N-2H-tetrazol-5-yl-

物理化學(xué)性質(zhì)

密度1.38±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)3.32±0.10(Predicted)

常見(jiàn)問(wèn)題列表

生物活性
CI-949 是一種過(guò)敏介質(zhì)釋放抑制劑,可抑制組胺 (histamine),白三烯 C4/D4 (LTC4/LTD4) 和血栓素 B2 (TXB2) 的釋放,IC50 分別為 11.4 μM,0.5 μM 和 0.1 μM。
靶點(diǎn)

TXB 2

0.1 μM (IC 50 )

LTC 4

0.5 μM (IC 50 )

LTD 4

0.5 μM (IC 50 )

Histamine

體外研究

CI-949 inhibits, in a dose-dependent manner, the release of histamine, leukotriene, and thromboxane from human basophilic leukocytes challenged with anti-IgE. The IC 50 for inhibition of histamine release is 11.4 μM. Virtually complete inhibition of histamine release occurs at 100 μM, with negligible inhibition of release <3 μM. Both LTC 4 /LTD 4 and TXB 2 release are inhibited at lower concentrations (IC 50 , 0.5 and 0.1 μM, respectively). Complete inhibition of leukotriene and thromboxane synthesis/release is obtained with 10 and 1 μM of CI-949, respectively. CI-949 is an effective inhibitor of release of all three mediators in response to this stimulus. The IC 50 s for inhibition of histamine, leukotriene, and thromboxane are 6.3, 2, and 0.1 μM for FMLP challenge. CI-949 effectively inhibits the release of histamine and the synthesis or release of immunoreactive sulfidopeptide leukotrienes C 4 -D 4 and thromboxane B 2 from antigen-challenged lung fragments of of actively sensitized guinea-pigs. The IC 50 s are 26.7±2.8 μM for histamine, 2.7±2.4 μM for leukotriene, and 3.0±1.8 μM for thromboxane.

體內(nèi)研究

Actively sensitized guinea-pigs are given i .p. doses of 30, 50, or 100 mg/kg of CI-949 between 20-120 min before aerosol challenge with antigen. A dose of 50 mg/kg i.p. of CI-949 protects conscious, aerosol-allergen challenged guinea-pigs for at least 1 h and 100 mg/kg i.p. or per os protects for at least 2 h. The animals are protected from collapse for at least I h after 50 and 100 mg/kg, and 100 mg/kg afforded complete protection up to 2h. An oral dose of 100 mg/kg at 2 h, but not at 4 h before challenge also inhibits collapse. A dose of 100 mg/kg at 4 h and again at 2 h before challenge is more effective than a single dose at 2 h.

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