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85547-56-4

中文名稱 磷酸哌喹
英文名稱 4,4'-(1,3-Propanediyldi-4,1-piperazinediyl)bis(7-chloroquinoline) phosphate
CAS 85547-56-4
分子式 C29H32Cl2N6.H3PO4
分子量 633.51
MOL 文件 85547-56-4.mol
更新日期 2026/07/10 13:10:23
85547-56-4 結(jié)構(gòu)式 85547-56-4 結(jié)構(gòu)式

基本信息

中文別名
磷酸喹哌
磷酸哌喹
哌喹磷酸鹽
1,3-雙[4-(7-氯-喹啉-4-基)哌嗪-1-基]丙烷磷酸鹽
英文別名
85547-56-4
PIPERAQUINE PHOSPHATE
antimalarial drugs PIPERAQUINE PHOSPHATE
2-(9-methyldecyl)-5-(4-methylpentyl)benzene-1,3-diol
4,4'-(1,3-Propanediyldi-4,1-piperazinediyl)bis(7-chloroquinoline)
4,4'-(1,3-propanediyldi-4,1-piperazinediyl)bis(7-chloroquinoline) phosphate
Quinoline, 4,4'-(1,3-propanediyldi-4,1-piperazinediyl)bis(7-chloro-, phosphate
4,4'-(1,3-Propanediyldi-4,1-piperazinediyl)bis(7-chloroquinoline) phosphate USP/EP/BP
所屬類別
原料藥:抗瘧藥

物理化學(xué)性質(zhì)

儲存條件-20°C儲存
溶解度DMSO: Insoluble;
形態(tài)Solid
顏色Off-white to light yellow
水溶解性Water: 2 mg/mL (3.16 mM)
InChIKeyKATNPMSTHHZOTK-UHFFFAOYSA-N
SMILESC(N1CCN(C2=C3C(=NC=C2)C=C(Cl)C=C3)CC1)CCN1CCN(C2=C3C(=NC=C2)C=C(Cl)C=C3)CC1.P(O)(O)(O)=O

安全數(shù)據(jù)

危險性符號(GHS)有害 (GHS07)
GHS07
警示詞警告
危險性描述H302
磷酸哌喹價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2026/07/06S5355磷酸哌喹
Piperaquine phosphate
85547-56-425mg794.54元
2026/06/05HY-B1896AR磷酸哌喹
Piperaquine phosphate (Standard)
85547-56-45 mg500元
2026/06/05HY-B1896AR磷酸哌喹
Piperaquine phosphate (Standard)
85547-56-410 mg800元

常見問題列表

生物活性
Piperaquine phosphate 是一種雙喹啉抗瘧藥,可以與青蒿素聯(lián)用于抗瘧研究。
體內(nèi)研究

Piperaquine (10-90 mg/kg; a single i.p.) decreases parasitemia at all of the doses tested in mice.
Piperaquine (90 mg/kg; a single i.p.) exhibits the t 1/2 , apparent clearance, and apparent volume of distribution 17.8 days, 33.5 mg?h/L, 1.55 L/h/kg, and 956 L/kg, respectively, in healthy mice and 16.1 days, 27.3 mg?h/L, 1.9 L/h/kg, and 1,059 L/kg in malaria-infected mice.

Animal Model: Male BALB/c mice (7 to 8 weeks) are inoculated with Plasmodium berghei parasites
Dosage: 0, 10, 30, 90 mg/kg
Administration: A single i.p. administration
Result: The median survival time was 10 days at dose of 10 mg/kg.
The median survival time was 54 days at dose of 30 mg/kg.
All mice were active and alert and had stable body weights throughout the course of the study at dose of 90 mg/kg.
Animal Model: Male Swiss mice (6 weeks old)
Dosage: 90 mg/kg (Pharmacokinetic Analysis)
Administration: A single i.p. administration
Result: t 1/2 =17.8 d; AUC=33.5 mg?h/L; apparent clearance=1.55 L/h/kg; apparent volume of distribution=956 L/kg.
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