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Merck

UC175

Sigma-Aldrich

(S)-(+)-美芬妥英

≥98% (HPLC), solid, CYP2B6 & CYP2C19 substrate

别名:

(S)-(+)-5-乙基-3-甲基-5-苯基-2,4-咪唑烷二酮, (S)-(+)-5-乙基-3-甲基-5-苯基海因

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About This Item

经验公式(希尔记法):
C12H14N2O2
CAS号:
分子量:
218.25
MDL號碼:
分類程式碼代碼:
12161501
PubChem物質ID:
NACRES:
NA.77

product name

(S)-(+)-美芬妥英, solid, ≥98% (HPLC)

化驗

≥98% (HPLC)

形狀

solid

顏色

off-white

mp

135-138 °C

溶解度

DMSO: soluble

儲存溫度

2-8°C

SMILES 字串

CC[C@]1(NC(=O)N(C)C1=O)c2ccccc2

InChI

1S/C12H14N2O2/c1-3-12(9-7-5-4-6-8-9)10(15)14(2)11(16)13-12/h4-8H,3H2,1-2H3,(H,13,16)/t12-/m0/s1

InChI 密鑰

GMHKMTDVRCWUDX-LBPRGKRZSA-N

應用

S-美芬妥因已被用作 CYP2C19 底物,用于分析细胞色素 P450 代谢。S-美芬妥因也被用作基于 LC/MS 的相对活性因子(RAF)分析的探针底物

生化/生理作用

CYP2B6 & CYP2C19 底物。Methenytoin 异构体。镇惊;抗癫痫。

特點和優勢

这种化合物是 ADME 毒性研究的特色产品。点击此处发现更多特色 ADME 毒性产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

包裝

无底玻璃瓶。内含物装在插入的融合锥内。

準備報告

(S)-(+)-美芬妥因可溶于 DMSO

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Brandon S Pybus et al.
Malaria journal, 11, 259-259 (2012-08-04)
The 8-aminoquinoline (8AQ) drug primaquine (PQ) is currently the only approved drug effective against the persistent liver stage of the hypnozoite forming strains Plasmodium vivax and Plasmodium ovale as well as Stage V gametocytes of Plasmodium falciparum. To date, several
Bent H Hellum et al.
Basic & clinical pharmacology & toxicology, 105(1), 58-63 (2009-04-18)
The aim of this study was to evaluate in vitro the dose-dependent induction potential of six commonly used trade herbal products on CYP2C19 and CYP2E1 metabolic activities in cultured human hepatocytes. S-mephenytoin and chlorzoxazone were used as specific CYP substrates
Stefan J Dekker et al.
British journal of pharmacology, 176(3), 466-477 (2018-11-18)
The aim of this study was to characterize the human cytochrome P450s (CYPs) involved in oxidative bioactivation of flucloxacillin to 5-hydroxymethyl flucloxacillin, a metabolite with high cytotoxicity towards biliary epithelial cells. The CYPs involved in hydroxylation of flucloxacillin were characterized

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