エフロルニチン

エフロルニチン 化学構造式
70050-56-5
CAS番号.
70050-56-5
化学名:
エフロルニチン
别名:
英語名:
2-(Difluoromethyl)-DL-ornithine
英語别名:
EFLORNITHINE;Eflornithine API;2-(Difluoromethyl)-DL-ornithine;alpha-Difluoromethylornithine hydrochloride;2,5-diamino-2-(difluoromethyl)valeric acid hydrochloride;2,5-diamino-2-(difluoromethyl)pentanoic acid hydrochloride;2,5-bis(azanyl)-2-(difluoromethyl)pentanoic acid hydrochloride
CBNumber:
CB62130510
化学式:
C6H12F2N2O2
分子量:
182.17
MOL File:
70050-56-5.mol

エフロルニチン 物理性質

融点 :
181-184 ºC

安全性情報

エフロルニチン 価格

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エフロルニチン 化学特性,用途語,生産方法

抗菌性

Cultured bloodstream trypomastigotes of T. brucei are relatively insensitive, but high doses are effective against bloodstream and CNS infections of T. brucei brucei and T. brucei gambiense in rodents, provided a strong antibody response is also present. Eflornithine entry into the CNS can be enhanced with suramin. T. brucei rhodesiense infections do not respond. Synergy with some arsenicals has been demonstrated.
Eflornithine is active against P. falciparum in experimental models and against Leishmania promastigotes and Giardia lamblia in culture.

獲得抵抗性

Acquired resistance in T. brucei gambiense in West Africa has not been reported. East African T. brucei rhodesiense strains are innately less sensitive. Reported treatment failures are thought to be associated with severity of disease.

応用例(製薬)

An analog of ornithine, formulated as the hydrochloride for intravenous infusion. It is freely soluble in water.

薬物動態学

Oral absorption: 55%
Cmax 10 mg/kg oral: c. 7 mg/L after 4 h
200 mg/kg intravenously: 15.9 mg/L (87.5 nmol/mL) (mean)
Plasma half-life: 3.3 h
Volume of distribution: 0.34 L/kg
Plasma protein binding: Very low
Renal clearance is 83%, with most eliminated unchanged. In a study in Zaire the mean serum concentration in children under 12 years old was half that of adults, probably due to more rapid renal clearance. CNS penetration is good in adult patients, with a CSF:plasma ratio of 0.91 at the end of administration for 14 days. However, the CSF:plasma ratio in children under 12 years old was 0.58. Relapses have been recorded in patients in whom CSF levels dropped below 9 mg/L (50 nmol/mL) at the end of treatment.

臨床応用

2-(Difluoromethyl)-DL-ornithine has been used speculatively for treatment of Pn. jirovecii infections in AIDS patients. Co-administration with oral nifurtimox has been added to the World Health Organization (WHO) List of Essential Medicines for second-stage sleeping sickness caused by T. brucei gambiense.

副作用

Osmotic diarrhea and bone marrow suppression are common, and up to 50% of sleeping sickness patients develop leukopenia. Reversible anemia and thrombocytopenia have been observed. Convulsions and seizures, different from those observed in melarsoprol-induced encephalopathy, have been reported in 4–18% of treated sleeping sickness patients but not in patients treated for Pn. jirovecii pneumonia. This difference might be due to the CNS inflammation associated with sleeping sickness.

エフロルニチン 上流と下流の製品情報

原材料

準備製品


エフロルニチン 生産企業

Global( 11)Suppliers
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CONIER CHEM AND PHARMA LIMITED
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Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 +86-13028896684;
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Sanover (Xiamen) Technology Co., Ltd 059265188632; 13876246362
422165847@qq.com China 510 58
Shaanxi Xihua Chemical Industry Co., Ltd 17691182729 15529505138
1021@dideu.com China 9969 58

70050-56-5(エフロルニチン)キーワード:


  • 70050-56-5
  • EFLORNITHINE
  • 2-(Difluoromethyl)-DL-ornithine
  • alpha-Difluoromethylornithine hydrochloride
  • 2,5-bis(azanyl)-2-(difluoromethyl)pentanoic acid hydrochloride
  • 2,5-diamino-2-(difluoromethyl)pentanoic acid hydrochloride
  • 2,5-diamino-2-(difluoromethyl)valeric acid hydrochloride
  • Eflornithine API
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