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31645-39-3

中文名稱 帕利伐米
英文名稱 Palifosfamide
CAS 31645-39-3
分子式 C4H11Cl2N2O2P
分子量 221.02
MOL 文件 31645-39-3.mol
更新日期 2024/08/19 09:28:05
31645-39-3 結(jié)構(gòu)式 31645-39-3 結(jié)構(gòu)式

基本信息

中文別名
帕利伐米
帕利伐米, >98%
N,N'-雙(2-氯乙基)二氨基膦酸
英文別名
Ipam
ZIO-201
Nsc 297900
palifosfamide
ZIO-201, >98%
Ifosforamide mustard
Isophosphamide mustard
Palifosfamide (ZIO-201)
Abbreviation: IPM-lysine
isophosphoramide mustard-lysine
所屬類別
原料藥

物理化學(xué)性質(zhì)

熔點106-107 ºC
沸點341.5±52.0 °C(Predicted)
密度1.411
儲存條件Store at -20°C, protect from light, stored under nitrogen
溶解度≥22.1 mg/mL in DMSO; insoluble in EtOH; ≥19.4 mg/mL in H2O with gentle warming and ultrasonic
酸度系數(shù)(pKa)0.79±0.50(Predicted)
形態(tài)粉末
顏色White to off-white
InChIInChI=1S/C4H11Cl2N2O2P/c5-1-3-7-11(9,10)8-4-2-6/h1-4H2,(H3,7,8,9,10)
InChIKeyBKCJZNIZRWYHBN-UHFFFAOYSA-N
SMILESP(NCCCl)(NCCCl)(O)=O
CAS 數(shù)據(jù)庫31645-39-3

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-H315-H319-H335

常見問題列表

概述
帕利伐米(IPM)是環(huán)磷酰胺(CPA)的常見代謝產(chǎn)物。帕利伐米被認為是CPA表現(xiàn)出的至少一部分抗腫瘤活性的原因。直接使用帕利伐米作為抗癌劑的努力未獲成功,部分原因是該化合物的不穩(wěn)定性。已經(jīng)合成了帕利伐米并且已經(jīng)對該化合物進行了初步的生物學(xué)評估,但遺憾的是帕利伐米太不穩(wěn)定而不能被分離并用于人類治療。
生物活性
Palifosfamide (ZIO-201, Isophosphamide mustard)是新型的DNA烷化劑,是異環(huán)磷酰胺(ifosfamide)的活性代謝產(chǎn)物,具有抗腫瘤活性。
體外研究

Palifosfamide lysine (ZIO-201) is a stable form of palifosfamide. Palifosfamide lysine has broad activity in sarcoma lines in vitro . The IC 50 ranges from 2.25 ro 6.75 μM for most cell lines except OS222 (IC 50 =31.5 μM).

體內(nèi)研究

Tumor growth inhibition is seen in both OS31 and OS33 xenografts and the RMS xenograft resulting in a significant difference in event-free survival between the control and the treated groups. Differential gene expression of ALDH3A1 but not ALDH1A1 is noted in the OS31 xenograft. Stabilized palifosfamide administered to mice suppresses MX-1 tumor growth by greater than 80% with 17% complete antitumor responses. Oral bioavailability in rats is 48-73% of parenteral administration, and antitumor activity in mice is equivalent by both routes. Treatment with palifosfamide-tris combined with docetaxelor doxorubicin at optimal regimens results in complete tumor regression in 62-75% of mice.

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