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202475-60-3

中文名称 4-(4'-羟基苯基)氨基-6,7-二甲氧基喹唑啉
英文名称 JAK3 INHIBITOR I
CAS 202475-60-3
分子式 C16H15N3O3
分子量 297.31
MOL 文件 202475-60-3.mol
更新日期 2024/04/22 19:07:08
202475-60-3 结构式 202475-60-3 结构式

基本信息

中文别名
JAK3抑制剂(JANEX-1)
4-(4'-羟基苯基)氨基-6,7-二甲氧基喹唑啉
4-(4\'-羟基苯基)氨基-6,7-二甲氧基喹唑啉, >98%
英文别名
CS-2623
Janex 1
WHI-P131
WHI-P131, >98%
JAK3 INHIBITOR I
JANEX-1
WHI-P131
WHI-P131(Janex 1)
A JAK3 inhibitor WHI-P131
WHIP-131
JANEX-1)
WHIP131
JANEX1
4-(6,7-dimethoxyquinazolin-4-ylamino)phenol
所属类别
生物化工:激动剂抑制剂

物理化学性质

沸点468.1±40.0 °C(Predicted)
密度1.336±0.06 g/cm3(Predicted)
储存条件Keep in dark place,Inert atmosphere,2-8°C
溶解度DMSO: 18 mg/mL, soluble
酸度系数(pKa)10.06±0.26(Predicted)
形态solid
颜色yellow
稳定性Stable for 2 years from date of purchase as supplied. Protect from moisture. Solutions in DMSO may be stored at -20°C for up to 2 months.

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335
危险品标志Xi
危险类别码36/37/38
安全说明26-36
WGK Germany3

常见问题列表

生物活性
JANEX-1 (WHI-P131)是JAK3小分子抑制剂,选择性抑制JAK3,IC50为78 μM。它不影响JAK1或JAK2,及其他蛋白酪氨酸激酶的活性(IC50 ≥ 350 µM)。
靶点
TargetValue
JAK3
(Cell-free assay)
78 μM
体外研究

JANEX-1 (WHI-P131) shows potent JAK3-inhibitory activity (IC 50 of 78 μM), does not inhibit JAK1 and JAK2, the ZAP/SYK family tyrosine kinase SYK, the TEC family tyrosine kinase BTK, the SRC family tyrosine kinase LYN, or the receptor family tyrosine kinase insulin receptor kinase, even at concentrations as high as 350 μM. JANEX-1 induces apoptosis in JAK3-expressing human leukemia cell lines NALM-6 and LC1;19 but not in melanoma (M24-MET) or squamous carcinoma (SQ20B) cells. WHI-P131 inhibits the clonogenic growth of JAK3-positive leukemia cell lines DAUDI, RAMOS, LC1;19, NALM-6, MOLT-3, and HL-60 (but not JAK3-negative BT-20 breast cancer, M24-MET melanoma, or SQ20B squamous carcinoma cell lines) in a concentration-dependent fashion. WHI-P131 inhibits clonogenic growth in a concentration-dependent fashion with EC 50 s of 24.4 μM for NALM-6 cells and 18.8 μM for DAUDI cells. At 100 μM, WHI-P131 inhibits the in vitro colony formation by these leukemia cell lines by >99%. In contrast, JANEX-1 does not inhibit the clonogenic growth of JAK3-negative M24-MET melanoma or SQ20B squamous carcinoma cell lines.

体内研究

JANEX-1 is administered at doses ranging from 5 to 100 mg/kg. Evaluation of CPK activity revealed a dose-response curve with an effective dose 50 (ED 50 ) value of 7.44 mg/kg. Mice receiving JANEX-1 displayed significantly reduced CPK and LDH levels. In addition, the infarct size of JANEX-1-treated mice (30.16±2.79%) is significantly decreased when compared with I/R-operated mice (65.64±3.76%). JANEX-1 (WHI-P131) is absorbed rapidly, and the time to reach the maximum plasma JANEX-1 concentration (t max ) is 24.7±1.7 min. JANEX-1 is rapidly eliminated with an elimination half-life of 45.6±5.5 min. Although the predicted maximum plasma JANEX-1 concentration is 10.5 ± 0.8 μM, which is only half of the C max following i.v. administration of the same bolus dose, the i.p. bioavailability is 94.6% and the systemic exposure levels (i.e., AUC) are very similar to those observed after i.v. injection (17.1±2.2 μM•h versus 18.1±1.2 μM•h).

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