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Antagonist G(trifluoroacetate salt)
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。
Antagonist G(trifluoroacetate salt)图片
规格:98%
分子量:951.2
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议

产品介绍
A neuropeptide antagonist
货号:ajcx25482
CAS:N/A
分子式:C49H66N12O6S·XCF3COOH
分子量:951.2
溶解度:DMF: 30 mg/ml,DMSO: 30 mg/ml,DMSO:PBS (pH 7.2) (1:3): 0.25 mg/ml,Ethanol: 20 mg/ml
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Antagonist G is a neuropeptide antagonist.1,2,3It inhibits the binding of vasopressin to rat liver or Swiss 3T3 membranes (IC50s = 3.5 and 2.2 µM, respectively) and vasopressin-induced production of inositol phosphate in Swiss 3T3 fibroblasts (IC50= 1 µM).1Antagonist G (50 µM) induces apoptosis and the production of reactive oxygen species (ROS) in NCI H69 small cell lung cancer (SCLC) cells.2It reduces tumor growth in an NCI H69 mouse xenograft model when administered at a dose of 45 µg/g.3


1.Seckl, M.J., Newman, R.H., Freemont, P.S., et al.Substance P-related antagonists inhibit vasopressin and bombesin but not 5’-3-O-(thio)triphosphate-stimulated inositol phosphate production in swiss 3T3 cellsJ. Cell Physiol.163(1)87-95(1995) 2.MacKinnon, A.C., Waters, C., Rahman, I., et al.[Arg6, D-Trp7,9, NmePhe8]-substance P (6-11) (antagonist G) induces AP-1 transcription and sensitizes cells to chemotherapyBr. J. Cancer.83(7)941-948(2000) 3.Langdon, S., Sethi, T., Ritchie, A., et al.Broad spectrum neuropeptide antagonists inhibit the growth of small cell lung cancer in vivoCancer Res.52(16)4554-4557(1992)