G63589 95058-81-4
Gemcitabine
溶解性 |
|
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存贮条件 | 储存温度-20°C |
密度 | 否 |
荧光 | 否 |
IC50 | 否 |
pK Values | 否 |
别名 | 吉西他滨; 4-氨基-1-[3,3-二氟-4-羟基-5-(羟甲基)氧杂环戊-2-基]嘧啶-2-酮;4-Amino-1-[3,3-difluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one |
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产品介绍 | 2‘-Deoxy-2‘,2‘-difluorocytidine is an irreversible inactivator of R1 and R2 (ribonucleoside diphosphate reductase, RDPR) from Escherichia coli. |
用途 | An irreversible inactivator of bacterial ribonucleoside diphosphate reductase. |
生化机理 |
Gemcitabine is a widely used antitumor agents in both clinics and research labs. It is an antineoplastic agent and antimetabolite. Gemcitabine is converted intracellularly to the active metabolites difluorodeoxycytidine di- and triphosphate (dFdCDP, dFdCTP). dFdCDP inhibits ribonucleotide reductase, thereby decreasing the deoxynucleotide pool available for DNA synthesis; dFdCTP is incorporated into DNA, resulting in DNA strand termination and apoptosis. Gemcitabine inhibits proliferation BxPC-3 pancreatic cancer cell line with IC50 of 0.06 μM. |
备注 | Gemcitabine(Gemzar) belongs to the group of medicines called antimetabolites. |
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