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202475-60-3

中文名稱 4-(4'-羥基苯基)氨基-6,7-二甲氧基喹唑啉
英文名稱 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 2024/12/24 22:26:10
202475-60-3 結(jié)構(gòu)式 202475-60-3 結(jié)構(gòu)式

基本信息

中文別名
JAK3抑制劑(JANEX-1)
4-(4'-羥基苯基)氨基-6,7-二甲氧基喹唑啉
4-(4\'-羥基苯基)氨基-6,7-二甲氧基喹唑啉, >98%
英文別名
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
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

沸點(diǎn)468.1±40.0 °C(Predicted)
密度1.336±0.06 g/cm3(Predicted)
儲(chǔ)存條件Keep in dark place,Inert atmosphere,2-8°C
溶解度DMSO: 18 mg/mL, soluble
酸度系數(shù)(pKa)10.06±0.26(Predicted)
形態(tài)solid
顏色yellow
穩(wěn)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.

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335
防范說(shuō)明P261-P305+P351+P338
危險(xiǎn)品標(biāo)志Xi
危險(xiǎn)類別碼36/37/38
安全說(shuō)明26-36
WGK Germany3

常見問(wèn)題列表

生物活性
JANEX-1 (WHI-P131)是JAK3小分子抑制劑,選擇性抑制JAK3,IC50為78 μM。它不影響JAK1或JAK2,及其他蛋白酪氨酸激酶的活性(IC50 ≥ 350 μM)。
靶點(diǎn)
TargetValue
JAK3
(Cell-free assay)
78 μM
體外研究

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.

體內(nèi)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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