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96187-53-0

中文名稱 布喹那
英文名稱 Brequinar
CAS 96187-53-0
分子式 C22H13F2NO2
分子量 375.37
MOL 文件 96187-53-0.mol
更新日期 2024/10/23 14:32:24
96187-53-0 結(jié)構(gòu)式 96187-53-0 結(jié)構(gòu)式

基本信息

中文別名
布喹那
布喹鈉
BREQUINAR 布喹那
6-氟-2-(2'-氟-[1,1'-聯(lián)苯]-4-基)-3-甲基喹啉-4-羧酸
DIHYDROOROTATE DEHYDROGENASE抑制劑(BREQUINAR)
英文別名
BPQ
CS-157
Brequinar
Biphenquinate
Brequinar (DUP785)
BREQUINAR
BIPENQUINATE
DUP 785
NSC 368390.
6-Fluoro-2-(2'-fluoro-[1,1'-biphenyl]-4-yl)
6-fluoro-2-(2'-fluorobiphenyl-4-yl)-3-Methylquinoline-4-carboxyl
6-fluoro-2-(2'-fluorobiphenyl-4-yl)-3-methylquinoline-4-carboxylic acid
6-fluoro-2-[4-(2-fluorophenyl)phenyl]-3-methylquinoline-4-carboxylic acid
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

熔點(diǎn)355-357℃ (N,N-dimethylformamide water )
儲(chǔ)存條件2-8°C
溶解度DMSO:25.9(Max Conc. mg/mL);70.0(Max Conc. mM)
酸度系數(shù)(pKa)pKa 4.45(H2O t=RT I=0.10) (Uncertain)
形態(tài)粉末晶體
顏色白色至淺黃色
CAS 數(shù)據(jù)庫96187-53-0

安全數(shù)據(jù)

危險(xiǎn)性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335
海關(guān)編碼2933.49.7000
布喹那價(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
2024/08/19HY-108325布喹那
Brequinar
96187-53-05mg700元
2024/08/19S6626布喹那
Brequinar (DUP785)
96187-53-05mg794.84元
2024/08/19HY-108325布喹那
Brequinar
96187-53-010mM * 1mLin DMSO770元

常見問題列表

生物活性
Brequinar (NSC 368390, DuP-785)是二氫乳清酸脫氫酶DHODH抑制劑,在體外IC50約為20 nM。
靶點(diǎn)
TargetValue
DHODH
()
20 nM
體外研究

Brequinar reduces virus progeny production by >90%, with EC 50 of 17 nM. Brequinar (5?μM) also inhibits other orthopoxviruses, and blocks virus DNA replication. Brequinar does not affect virus early gene expression, but has a severe effect on the late stage of the virus cycle. Brequinar reduces the level of envelope protein production and the viral titer in a dose-dependent manner, with EC 50 of 78 nM in the CFI assay. Brequinar (5 μM) inhibits viral RNA synthesis. Brequinar has antiviral effect, but the effect is reversed by pyrimidine. Brequinar-resistant viruses can be selected in cell culture. Brequinar (5 μM) suppresses the luciferase activities from both the WT and NS5 mutant replicons. Brequinar sodium effectively prevents the increase in PyNTP levels with an IC 50 of 0.26 μM. Brequinar sodium effectively inhibits cell proliferation with an IC 50 of 0.26 μM. Brequinar sodium inhibits autophosphorylation of p56 lck with IC 50 of 70 μM; inhibition is 39, 41, and 60% for 25, 50, and 100 μM Brequinar sodium, respectively. Brequinar sodium also inhibits the phosphorylation by p56 lck of the exogenous substrate, histone 2B, with an IC 50 of 70 μM; inhibition is 10, 43, 59, and 86% for 25, 50, 100, and 200 μM Brequinar sodium, respectively. Brequinar sodium inhibits autophosphorylation of p59 fyn with an IC 50 of 105 μM; inhibition is 0, 17, 48, and 65% for 25, 50, 100, and 200 μM Brequinar sodium, respectively. Brequinar sodium also inhibits the phosphorylation by p59 fyn of histone 2B with an IC 50 of 20 μM; inhibition is 26, 54, 79, 83, and 84% for 10, 25, 50, 100, and 200 μM Brequinar sodium, respectively.

體內(nèi)研究

Brequinar sodium-treated (10-20 mg/kg/day) mice has a 31% reduction in percentage of packed cell volume compared with untreated BALB/c mice. Brequinar sodium reduces UTP and CTP levels in bone marrow cells by 30 and 25%, respectively. Brequinar sodium (10-20 mg/kg/day) in combination with uridine (1000-2000 mg/kg/day) prevents anemia, and the hematocrits remain at levels (61-63%) comparable with those of untreated controls.

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