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Merck
CN

M5571

Sigma-Aldrich

米替福新

≥98% (perchloric acid titration)

别名:

十六烷基胆碱磷酸(抗肿瘤药), 肝细胞癌, 胆碱十六烷基磷酸酯

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About This Item

经验公式(希尔记法):
C21H46NO4P
CAS号:
分子量:
407.57
MDL编号:
UNSPSC代码:
51191904
PubChem化学物质编号:
NACRES:
NA.85

生物来源

synthetic (organic)

质量水平

描述

zwitterionic

方案

≥98% (perchloric acid titration)

表单

powder

溶解性

H2O: 10 mg/mL, clear, colorless

官能团

phospholipid

脂质类型

phospholipids

储存温度

room temp

SMILES字符串

[O-]P(OCC[N+](C)(C)C)(OCCCCCCCCCCCCCCCC)=O

InChI

1S/C21H46NO4P/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-25-27(23,24)26-21-19-22(2,3)4/h5-21H2,1-4H3

InChI key

PQLXHQMOHUQAKB-UHFFFAOYSA-N

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应用


  • 作为一类新型抗利什曼原虫药物的多功能化吲哚吡咯杂化物的简易一锅法合成。: 这项研究强调了在患者对已知药物(如用作阳性对照参考品的米替福新)的耐药性日益增强的情况下,创新治疗的必要性,这可能为抗利什曼原虫药物的开发开辟新的方向(Ciccone et al., 2024)。

生化/生理作用

蛋白激酶C和磷脂酰胆碱合成抑制剂。用于内脏和皮肤利什曼病的治疗。对阴道毛滴虫甲硝唑耐药株和敏感株有效

象形图

Skull and crossbones

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Oral

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Thomas P C Dorlo et al.
Antimicrobial agents and chemotherapy, 52(8), 2855-2860 (2008-06-04)
The pharmacokinetics of miltefosine in leishmaniasis patients are, to a great extent, unknown. We examined and characterized the pharmacokinetics of miltefosine in a group of patients with Old World (Leishmania major) cutaneous leishmaniasis. Miltefosine plasma concentrations were determined in samples
Suresh K Tipparaju et al.
Journal of medicinal chemistry, 51(23), 7344-7347 (2008-11-08)
The first synthesis and biological evaluation of antibiotic 31 (A-33853) and its analogues are reported. Initial screening for inhibition of L. donovani, T. b. rhodesiense, T. cruzi, and P. falciparum cultures followed by determination of IC(50) in L. donovani and
Nathan P Wiederhold et al.
Antimicrobial agents and chemotherapy, 57(2), 745-750 (2012-11-21)
Miltefosine is an alkyl phosphocholine with good oral bioavailability and in vitro activity against Cryptococcus species that has gained interest as an additional agent for cryptococcal infections. Our objective was to further evaluate the in vivo efficacy of miltefosine in
Maria V Papadopoulou et al.
Journal of medicinal chemistry, 54(23), 8214-8223 (2011-10-26)
A series of novel 2-nitro-1H-imidazole- and 3-nitro-1H-1,2,4-triazole-based aromatic and aliphatic amines were screened for antitrypanosomal activity and mammalian cytotoxicity by the Drugs for Neglected Diseases initiative (DNDi). Out of 42 compounds tested, 18 3-nitro-1,2,4-triazoles and one 2-nitroimidazole displayed significant growth
Abdullah Alotaibi et al.
Scientific reports, 9(1), 11364-11364 (2019-08-08)
Extracts of 35 samples of European propolis were tested against wild type and resistant strains of the protozoal pathogens Trypanosoma brucei, Trypanosoma congolense and Leishmania mexicana. The extracts were also tested against Crithidia fasciculata a close relative of Crithidia mellificae

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