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Lonidamine(AF-1890)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Lonidamine(AF-1890)图片
CAS NO:50264-69-2
规格:≥98%
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)321.16
FormulaC15H10Cl2N2O2
CAS No.50264-69-2
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 64 mg/mL (199.3 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Other info

Chemical Name: 1-(2,4-dichlorobenzyl)-1H-indazole-3-carboxylic acid

InChi Key: WDRYRZXSPDWGEB-UHFFFAOYSA-N

InChi Code: InChI=1S/C15H10Cl2N2O2/c16-10-6-5-9(12(17)7-10)8-19-13-4-2-1-3-11(13)14(18-19)15(20)21/h1-7H,8H2,(H,20,21)

SMILES Code: O=C(C1=NN(CC2=CC=C(Cl)C=C2Cl)C3=C1C=CC=C3)O

SynonymsAF 1890; AF1890; AF-1890; Diclondazolic Acid; DICA; Diclondazolic acid; Doridamina; Lonidamine
实验参考方法
In Vitro

In vitro activity: Lonidamine reduces the oxygen consumption in both normal and neoplastic cells, while it increases the aerobic glycolysis of normal cells but inhibited that of tumor cells. Lonidamine induces the permeabilization of ANT proteoliposomes in a cell-free system, yet has no effect on protein-free liposomes. Lonidamine adds to synthetic planar lipid bilayers containing ANT, eliciting ANT channel activities with clearly distinct conductance levels. Lonidamine provokes a disruption of the mitochondrial transmembrane potential which precedes signs of nuclear apoptosis and cytolysis. Lonidamine causes the dissipation of the mitochondrial inner transmembrane potential and the release of apoptogenic factors capable of inducing nuclear apoptosis in vitro. Lonidamine (50 mg/mL) induces apoptosis in adriamycin and nitrosourea-resistant cells (MCF-7 ADR(r) human breast cancer cell line, and LB9 glioblastoma multiform cell line), as demonstrated by sub-G1 peaks in DNA content histograms, condensation of nuclear chromatin, and internucleosomal DNA fragmentation. Lonidamine has a stronger effect on glioblastoma cell proliferation and metabolism in vitro than did either agent used alone.

In VivoLonidamine (160 mg/kg) combined with Diazepam is significantly more effective in reducing glioblastoma tumor growth than either drug alone in mice, this tumor growth retardation is maintained as long as treatment is given.
Animal modelMice
Formulation & Dosage160 mg/kg
References

J Natl Cancer Inst. 1981 Mar;66(3):497-9; Oncogene. 2001 Nov 15;20(52):7579-87; J Natl Cancer Inst. 1998 Sep 16;90(18):1400-6.