CAS NO: | 146464-95-1 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
Pralatrexate is anantifolateand is a potentdihydrofolate reductasean (DHFR)inhibitor with aKiof 13.4 pM. Pralatrexate is a substrate for folylpolyglutamate synthetase with improved cellular uptake and retention. Pralatrexate has antitumor activities and has the potential for relapsed/refractory T-cell lymphoma treatment[1][2][3][4]. |
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IC50& Target |
Ki: 13.4 pM (Dihydrofolate reductasean (DHFR))[4] |
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体外研究 (In Vitro) |
Pralatrexate (100 pM-200 μM; 48-72 hours; T-lymphoma cell lines) treatment exhibits concentration- and time-dependent cytotoxicity against a broad panel of T-lymphoma cell lines. The IC50values at 48 and 72 hours, respectively, are as follows: H9 cells, 1.1 nM and 2.5 nM; P12 cells, 1.7 nM and 2.4 nM; CEM cells, 3.2 nM and 4.2 nM; PF-382 cells, 5.5 nM and 2.7 nM; KOPT-K1 cells, 1 nM and 1.7 nM; DND-41 cells, 97.4 nM and 1.2 nM; and HPB-ALL cells, 247.8 nM and 0.77 nM. HH cells are relatively resistant after 48 hours of exposure, with the IC50at 72 hours being 2.8 nM[1].
Cell Cytotoxicity Assay[1]
Apoptosis Analysis[1]
Western Blot Analysis[1]
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体内研究 (In Vivo) |
The addition of Pralatrexate (15 mg/kg; intraperitoneal injection; on days 1, 4, 8, and 11; SCID-beige mice) to Bortezomib (0.5 mg/kg) enhanced efficacy compared with either drug alone[1].
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Clinical Trial |
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分子量 |
477.47 |
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性状 |
Solid |
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Formula |
C23H23N7O5 |
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CAS 号 |
146464-95-1 |
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中文名称 |
普拉曲沙 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : ≥ 50 mg/mL(104.72 mM) *"≥" means soluble, but saturation unknown.
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In Vivo:
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