成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

返回ChemicalBook首頁>CAS數(shù)據(jù)庫列表>86-34-0

86-34-0

中文名稱 密朗丁
英文名稱 PHENSUXIMIDE
CAS 86-34-0
分子式 C11H11NO2
分子量 189.21
MOL 文件 86-34-0.mol
更新日期 2024/12/31 13:21:53
86-34-0 結(jié)構(gòu)式 86-34-0 結(jié)構(gòu)式

基本信息

中文別名
密朗丁
米浪丁
苯琥胺
苯琥胺 USP標(biāo)準(zhǔn)品
1-甲基-3-苯基-2,5-吡咯烷二酮
1-甲基-3-苯基吡咯烷-2,5-二酮
英文別名
pm334
Lifen
Epimid
Lifene
PM 334
Epimal
Mirotin
Milontin
Milonton
Mirontin
所屬類別
原料藥:抗癲癇及抗驚厥藥

物理化學(xué)性質(zhì)

熔點71-73°
沸點324.47°C (rough estimate)
密度1.1596 (rough estimate)
折射率1.5012 (estimate)
儲存條件Refrigerator
溶解度氯仿(微溶)、乙酸乙酯(微溶)
酸度系數(shù)(pKa)-1.86±0.40(Predicted)
形態(tài)固體
顏色白色至灰白色
水溶解性4.2g/L(25 ºC)

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302
防范說明P301+P312+P330
海關(guān)編碼2925190100
毒性LD50 orally in mice: 960 mg/kg (Chen, Ensor)

常見問題列表

生物活性
Phensuximide 是一種琥珀酰亞胺類抗癲癇 (antiepileptic) 和抗驚厥 (anticonvulsant) 試劑。Phensuximide 可以抑制去極化腦組織中 cyclic AMP 和 cyclic GMP 的積累。在動物模型中,Phensuximide 可用于癲癇研究的相關(guān)研究。
靶點

IC50: cyclic AMP and cyclic GMP accumulation

體外研究

Phensuximide produce depolarization-induced accumulation of cyclic GMP or cyclic AMP levels with ID 50 values of 8.00 mM or 6.20 mM in incubated slices of mouse cerebral cortex.Phensuximide (0.5-2.0 mM) has the ability to competitively inhibit mephenytoin 4-hydroxylase activity in human liver microsomes, the K i and K m values are 559 μM and 235 μM, respectively.

體內(nèi)研究

Phensuximide (intraperitoneal injection; 1.25 mmol/kg; single dose) induces mild changes in renal function, including: trace hematuria, increased proteinuria and decreased paminohippurate uptake in Sprague-Dawley rats.Phensuximide (intraperitoneal injection; 0.3 or 0.6 mmol/kg; 5-7 days) results in transient hematuria and proteinuria, but no change in the other renal function parameters studied. It is concluded that phensuximide produces mild, transient renal effects in Fischer 344 rats, and that the Fischer 344 rat is a suitable model for studying phensuximide-induced toxicity to the urinary tract.

Animal Model: Fischer 344 rats
Dosage: 0.3 or 0.6 mmol/kg
Administration: Intraperitoneal injection; 5-7 days
Result: Induced urotoxicity following daily administration for 5-7 days in Fischer 344 rats.
"86-34-0" 相關(guān)產(chǎn)品信息