1. Cell Cycle/DNA Damage Autophagy
  2. Antifolate Autophagy
  3. Pemetrexed

Pemetrexed  (Synonyms: 培美曲塞; LY231514)

目录号: HY-10820 纯度: 99.91%
COA 产品使用指南

Pemetrexed (LY231514) 是一种叶酸拮抗剂 (antifolate)。Pemetrexed (LY231514) 抑制胸苷酸合成酶 (TS),二氢叶酸还原酶 (DHFR) 和甘氨酰胺核苷酸甲酰转移酶 (GARFT),Ki 分别为 1.3 nM,7.2 nM 和 65 nM。

MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Pemetrexed Chemical Structure

Pemetrexed Chemical Structure

CAS No. : 137281-23-3

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规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥770
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50 mg ¥825
In-stock
100 mg ¥1250
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Customer Review

    Pemetrexed purchased from MCE. Usage Cited in: Theranostics. 2020 May 15;10(13):6048-6060.  [Abstract]

    Immunofluorescence assay showing the expression and intracellular location of UCHL1 in NSCLC cells. Increased UCHL1 levels are observed in both the cytoplasm and the nucleus of the PEM-R cells.

    Pemetrexed purchased from MCE. Usage Cited in: Theranostics. 2020 May 15;10(13):6048-6060.  [Abstract]

    Western blot analysis of UCHL1 levels in PEM-R cells and their parental cells. The mRNA and protein levels of UCHL1 in the PEM-R cells are significantly increased, relative to in the parental cells.
    • 生物活性

    • 实验参考方法

    • 纯度 & 产品资料

    • 参考文献

    生物活性

    Pemetrexed (LY231514) is an antifolate, the Ki values of the pentaglutamate of Pemetrexed (LY231514) are 1.3, 7.2, and 65 nM for inhibits thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), respectively[1].

    IC50 & Target

    Ki: 1.3 nM (TS), 7.2 nM (DHFR), 65 nM (GARFT)[1]

    细胞效力
    (Cellular Effect)
    Cell Line Type Value Description References
    A2780 IC50
    39.4 nM
    Compound: PMX
    Antiproliferative activity against human A2780 cells after 96 hrs by Cell-Titer Blue assay
    Antiproliferative activity against human A2780 cells after 96 hrs by Cell-Titer Blue assay
    [PMID: 29701475]
    A549 IC50
    0.08 μM
    Compound: PMX
    Cytotoxicity against human A549 cells assessed as growth inhibition after 72 hrs by MTT assay
    Cytotoxicity against human A549 cells assessed as growth inhibition after 72 hrs by MTT assay
    [PMID: 25668494]
    A549 IC50
    1.26 μM
    Compound: PMX
    Antiproliferative activity against human A549 cells after 72 hrs by MTT assay in presence of leucovorin
    Antiproliferative activity against human A549 cells after 72 hrs by MTT assay in presence of leucovorin
    [PMID: 27017552]
    A549 IC50
    1260 nM
    Compound: PMX
    Antiproliferative activity against human A549 cells assessed as reduction in cell viability after 72 hrs by MTT assay
    Antiproliferative activity against human A549 cells assessed as reduction in cell viability after 72 hrs by MTT assay
    [PMID: 31200235]
    A549 IC50
    3.31 μM
    Compound: PTX
    Antiproliferative activity against human A549 cells after 24 hrs by MTT assay
    Antiproliferative activity against human A549 cells after 24 hrs by MTT assay
    [PMID: 29807332]
    HepG2 IC50
    1.26 μM
    Compound: PMX
    Cytotoxicity against human HepG2 cells assessed as growth inhibition after 72 hrs by MTT assay
    Cytotoxicity against human HepG2 cells assessed as growth inhibition after 72 hrs by MTT assay
    [PMID: 25668494]
    HUVEC IC50
    1.73 μM
    Compound: PMX
    Cytotoxicity against HUVEC assessed as reduction in cell viability after 72 hrs by MTT assay
    Cytotoxicity against HUVEC assessed as reduction in cell viability after 72 hrs by MTT assay
    [PMID: 31200235]
    IGROV-1 IC50
    > 20 μM
    Compound: PMX
    Anticlonogenic activity against human IGROV1 cells incubated for 24 hrs followed by compound wash out and measured after 10 days by methylene blue staining-based assay
    Anticlonogenic activity against human IGROV1 cells incubated for 24 hrs followed by compound wash out and measured after 10 days by methylene blue staining-based assay
    [PMID: 29701475]
    IGROV-1 IC50
    102 nM
    Compound: PMX, LY-231514
    Antiproliferative activity against human IGROV1 cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs
    Antiproliferative activity against human IGROV1 cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs
    [PMID: 21879757]
    IGROV-1 IC50
    104 nM
    Compound: PMX
    Antiproliferative activity against wild type human IGROV1 cells after 96 hrs by Cell-Titer Blue assay
    Antiproliferative activity against wild type human IGROV1 cells after 96 hrs by Cell-Titer Blue assay
    [PMID: 29701475]
    IGROV-1 IC50
    200 nM
    Compound: PMX, LY-231514
    Antiproliferative activity against human IGROV1 cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs in the presence of 200 nM folic acid
    Antiproliferative activity against human IGROV1 cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs in the presence of 200 nM folic acid
    [PMID: 21879757]
    IGROV-1 IC50
    22.2 nM
    Compound: PMX
    Antiproliferative activity against FRalpha knockout human IGROV1 KD10 cells after 96 hrs by Cell-Titer Blue assay
    Antiproliferative activity against FRalpha knockout human IGROV1 KD10 cells after 96 hrs by Cell-Titer Blue assay
    [PMID: 29701475]
    IGROV-1 IC50
    46.6 nM
    Compound: PMX
    Antiproliferative activity against FRalpha knockout human IGROV1 KD4 cells after 96 hrs by Cell-Titer Blue assay
    Antiproliferative activity against FRalpha knockout human IGROV1 KD4 cells after 96 hrs by Cell-Titer Blue assay
    [PMID: 29701475]
    IGROV-1 IC50
    71 nM
    Compound: PMX
    Antiproliferative activity against human IGROV1 cells harboring non targeted control shRNA sequence after 96 hrs by Cell-Titer Blue assay
    Antiproliferative activity against human IGROV1 cells harboring non targeted control shRNA sequence after 96 hrs by Cell-Titer Blue assay
    [PMID: 29701475]
    KB IC50
    0.07 μM
    Compound: PMX
    Cytotoxicity against human KB cells assessed as growth inhibition after 72 hrs by MTT assay
    Cytotoxicity against human KB cells assessed as growth inhibition after 72 hrs by MTT assay
    [PMID: 25668494]
    KB IC50
    0.07 μM
    Compound: PMX
    Antiproliferative activity against human KB cells after 72 hrs by MTT assay in presence of leucovorin
    Antiproliferative activity against human KB cells after 72 hrs by MTT assay in presence of leucovorin
    [PMID: 27017552]
    KB IC50
    11.74 nM
    Compound: 6, Pemetrexed, PMX, Alimta
    Inhibition of GARFTase in human KB cells assessed as incorporation of [14C]-glycine into [14C]-formyl GAR incubated 30 mins prior to [14C]-glycine addition measured after 16 hrs by radiometric assay in presence of azaserin
    Inhibition of GARFTase in human KB cells assessed as incorporation of [14C]-glycine into [14C]-formyl GAR incubated 30 mins prior to [14C]-glycine addition measured after 16 hrs by radiometric assay in presence of azaserin
    [PMID: 24256410]
    KB IC50
    11.74 nM
    Compound: PMX, LY231514
    Inhibition of GARFTase in human KB cells expressing RFC/FRalpha/PCFT assessed as incorporation of [U-14C]-glycine into [14C]-formyl glycinamide ribonucleotide incubated for 1 hr followed by [U-14C]-glycine addition measured after 16 hrs
    Inhibition of GARFTase in human KB cells expressing RFC/FRalpha/PCFT assessed as incorporation of [U-14C]-glycine into [14C]-formyl glycinamide ribonucleotide incubated for 1 hr followed by [U-14C]-glycine addition measured after 16 hrs
    [PMID: 25602637]
    KB IC50
    30 nM
    Compound: PMX
    Inhibition of GARFTase in human KB cells assessed as inhibition of incorporation of [14C]glycine into [14C]formyl GAR after 30 mins in presence of azaserine
    Inhibition of GARFTase in human KB cells assessed as inhibition of incorporation of [14C]glycine into [14C]formyl GAR after 30 mins in presence of azaserine
    [PMID: 19371039]
    KB IC50
    30 μM
    Compound: PMX
    Inhibition of GARFtase in human KB cells assessed as [14C]glycine incorporation in to [14C]FGAR in folate free RPMI medium with 2 nM LCV by in-situassay
    Inhibition of GARFtase in human KB cells assessed as [14C]glycine incorporation in to [14C]FGAR in folate free RPMI medium with 2 nM LCV by in-situassay
    [PMID: 20085328]
    KB IC50
    327 nM
    Compound: PMX
    Inhibition of DHFR in human KB cells expressing RFC/FRalpha/PCFT assessed as reduction in cell growth after 96 hrs in presence of folic acid by Cell-Titer Blue assay
    Inhibition of DHFR in human KB cells expressing RFC/FRalpha/PCFT assessed as reduction in cell growth after 96 hrs in presence of folic acid by Cell-Titer Blue assay
    [PMID: 32503687]
    KB IC50
    327 nM
    Compound: PMX
    Antiproliferative activity against human KB cells expressing human RFC/FR-alpha/PCFT assessed as reduction in cell viability measured after 96 hrs in presence of folic acid by Cell-Titer Blue assay
    Antiproliferative activity against human KB cells expressing human RFC/FR-alpha/PCFT assessed as reduction in cell viability measured after 96 hrs in presence of folic acid by Cell-Titer Blue assay
    [PMID: 29425443]
    KB IC50
    327 nM
    Compound: PMX, pemetrexed
    Growth inhibition of human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTiter-blue assay in presence of folic acid
    Growth inhibition of human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTiter-blue assay in presence of folic acid
    [PMID: 24111942]
    KB IC50
    327 nM
    Compound: PMX
    Cytotoxicity against human KB cells assessed as cell growth inhibition incubated up to 96 hrs in presence of 200 nM folic acid by Celltiter-blue cell viability assay
    Cytotoxicity against human KB cells assessed as cell growth inhibition incubated up to 96 hrs in presence of 200 nM folic acid by Celltiter-blue cell viability assay
    [PMID: 25234128]
    KB IC50
    327 nM
    Compound: PMX, LY-231514
    Antiproliferative activity against human KB cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs in the presence of 200 nM folic acid
    Antiproliferative activity against human KB cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs in the presence of 200 nM folic acid
    [PMID: 21879757]
    KB IC50
    68 nM
    Compound: PMX
    Inhibition of DHFR in human KB cells expressing RFC/FRalpha/PCFT assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
    Inhibition of DHFR in human KB cells expressing RFC/FRalpha/PCFT assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
    [PMID: 32503687]
    KB IC50
    68 nM
    Compound: PMX
    Antiproliferative activity against human KB cells expressing human RFC/FR-alpha/PCFT assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue assay
    Antiproliferative activity against human KB cells expressing human RFC/FR-alpha/PCFT assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue assay
    [PMID: 29425443]
    KB IC50
    68 nM
    Compound: PMX, LY231514
    Antiproliferative activity against human KB cells expressing RFC/FRalpha/PCFT after 96 hrs by CellTiter-Blue assay
    Antiproliferative activity against human KB cells expressing RFC/FRalpha/PCFT after 96 hrs by CellTiter-Blue assay
    [PMID: 25602637]
    KB IC50
    68 nM
    Compound: PMX, pemetrexed
    Growth inhibition of human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTiter-blue assay
    Growth inhibition of human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTiter-blue assay
    [PMID: 24111942]
    KB IC50
    68 nM
    Compound: PMX, LY-231514
    Antiproliferative activity against human KB cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs
    Antiproliferative activity against human KB cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs
    [PMID: 21879757]
    KB IC50
    68 nM
    Compound: PMX
    Cytotoxicity against human KB cells assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
    Cytotoxicity against human KB cells assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
    [PMID: 25234128]
    KB IC50
    690 nM
    Compound: 6, Pemetrexed, PMX, Alimta
    Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay in presence of folic acid
    Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay in presence of folic acid
    [PMID: 24256410]
    KB IC50
    70.2 nM
    Compound: PMX
    Antiproliferative activity against human KB cells assessed as reduction in cell viability after 72 hrs by MTT assay
    Antiproliferative activity against human KB cells assessed as reduction in cell viability after 72 hrs by MTT assay
    [PMID: 31200235]
    KB IC50
    9.94 nM
    Compound: 6, Pemetrexed, PMX, Alimta
    Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay
    Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay
    [PMID: 24256410]
    MCF7 IC50
    0.65 μM
    Compound: PMX
    Antiproliferative activity against human MCF7 cells in folate free medium after 72 hrs in presence of leucovorin by MTT assay
    Antiproliferative activity against human MCF7 cells in folate free medium after 72 hrs in presence of leucovorin by MTT assay
    [PMID: 28830032]
    MDA-MB-231 IC50
    3.85 μM
    Compound: PTX
    Antiproliferative activity against human MDA-MB-231 cells after 24 hrs by MTT assay
    Antiproliferative activity against human MDA-MB-231 cells after 24 hrs by MTT assay
    [PMID: 29807332]
    OVCAR-3 IC50
    6.9 μM
    Compound: PTX
    Antiproliferative activity against human OVCAR3 cells after 24 hrs by MTT assay
    Antiproliferative activity against human OVCAR3 cells after 24 hrs by MTT assay
    [PMID: 29807332]
    R2 IC50
    > 1000 nM
    Compound: 6, Pemetrexed, PMX, Alimta
    Cytotoxicity against chinese hamster R2 cells after 96 hrs by CellTitre-Blue fluorescence assay
    Cytotoxicity against chinese hamster R2 cells after 96 hrs by CellTitre-Blue fluorescence assay
    [PMID: 24256410]
    R2 IC50
    13.2 nM
    Compound: PMX
    Inhibition of DHFR in Chinese Hamster MTXRII-OuaR2-4 R2 cells expressing human PCFT assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
    Inhibition of DHFR in Chinese Hamster MTXRII-OuaR2-4 R2 cells expressing human PCFT assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
    [PMID: 32503687]
    R2 IC50
    13.2 nM
    Compound: PMX, pemetrexed
    Growth inhibition of Chinese hamster R2 cells expressing human PCFT4 after 96 hrs by CellTiter-blue assay
    Growth inhibition of Chinese hamster R2 cells expressing human PCFT4 after 96 hrs by CellTiter-blue assay
    [PMID: 24111942]
    R2 IC50
    13.2 nM
    Compound: PMX, LY-231514
    Antiproliferative activity against chinese hamster R2 cells expressing human PCFT assessed as reduction of viable cells after 96 hrs
    Antiproliferative activity against chinese hamster R2 cells expressing human PCFT assessed as reduction of viable cells after 96 hrs
    [PMID: 21879757]
    R2 IC50
    138 nM
    Compound: PMX
    Antiproliferative activity in Chinese hamster R2 cells deficient in RFC, PCFT, and FRalpha assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
    Antiproliferative activity in Chinese hamster R2 cells deficient in RFC, PCFT, and FRalpha assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
    [PMID: 29701475]
    R2 IC50
    22.3 nM
    Compound: 6, Pemetrexed, PMX, Alimta
    Cytotoxicity against chinese hamster R2 cells expressing human PCFT4 after 96 hrs by CellTitre-Blue fluorescence assay
    Cytotoxicity against chinese hamster R2 cells expressing human PCFT4 after 96 hrs by CellTitre-Blue fluorescence assay
    [PMID: 24256410]
    R2 IC50
    4.94 nM
    Compound: PMX, LY-231514
    Antiproliferative activity against chinese hamster R2 cells expressing human PCFT assessed as inhibition of colony formation after 10 to 14 days
    Antiproliferative activity against chinese hamster R2 cells expressing human PCFT assessed as inhibition of colony formation after 10 to 14 days
    [PMID: 21879757]
    R2 IC50
    42 nM
    Compound: PMX, LY231514
    Cytotoxicity against RFC-deficient Chinese hamster R2 cells assessed as growth inhibition after 96 hrs by CellTiter-Blue assay
    Cytotoxicity against RFC-deficient Chinese hamster R2 cells assessed as growth inhibition after 96 hrs by CellTiter-Blue assay
    [PMID: 25602637]
    R2 IC50
    42 nM
    Compound: PMX
    Cytotoxicity in RFC-null Chinese hamster R2 cells assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue fluorescence analysis
    Cytotoxicity in RFC-null Chinese hamster R2 cells assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue fluorescence analysis
    [PMID: 27458733]
    R2 IC50
    849 nM
    Compound: PMX
    Cytotoxicity in RFC-null Chinese hamster R2 cells assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue assay
    Cytotoxicity in RFC-null Chinese hamster R2 cells assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue assay
    [PMID: 29425443]
    R2 IC50
    894 nM
    Compound: PMX
    Inhibition of DHFR in Chinese Hamster MTXRII-OuaR2-4/FRalpha-null R2 cells assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
    Inhibition of DHFR in Chinese Hamster MTXRII-OuaR2-4/FRalpha-null R2 cells assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
    [PMID: 32503687]
    R2 IC50
    894 nM
    Compound: PMX, LY-231514
    Antiproliferative activity against chinese hamster R2 cells assessed as reduction of viable cells after 96 hrs
    Antiproliferative activity against chinese hamster R2 cells assessed as reduction of viable cells after 96 hrs
    [PMID: 21879757]
    R2 IC50
    894 nM
    Compound: PMX
    Cytotoxicity against Chinese hamster R2 cells assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
    Cytotoxicity against Chinese hamster R2 cells assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
    [PMID: 25234128]
    R2 IC50
    974 nM
    Compound: PMX
    Cytotoxicity against Chinese hamster R2 cells expressing empty vector assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
    Cytotoxicity against Chinese hamster R2 cells expressing empty vector assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
    [PMID: 25234128]
    SGC-7901 IC50
    9.08 μM
    Compound: PTX
    Antiproliferative activity against human SGC7901 cells after 24 hrs by MTT assay
    Antiproliferative activity against human SGC7901 cells after 24 hrs by MTT assay
    [PMID: 29807332]
    SW-620 IC50
    0.08 μM
    Compound: PMX
    Antiproliferative activity against human SW620 cells after 72 hrs by MTT assay in presence of leucovorin
    Antiproliferative activity against human SW620 cells after 72 hrs by MTT assay in presence of leucovorin
    [PMID: 27017552]
    SW-620 IC50
    0.09 μM
    Compound: PMX
    Antiproliferative activity against human SW620 cells in folate free medium after 72 hrs in presence of leucovorin by MTT assay
    Antiproliferative activity against human SW620 cells in folate free medium after 72 hrs in presence of leucovorin by MTT assay
    [PMID: 28830032]
    SW-620 IC50
    80.2 nM
    Compound: PMX
    Antiproliferative activity against human SW620 cells assessed as reduction in cell viability after 72 hrs by MTT assay
    Antiproliferative activity against human SW620 cells assessed as reduction in cell viability after 72 hrs by MTT assay
    [PMID: 31200235]
    体外研究
    (In Vitro)

    Pemetrexed (LY231514) 是一种新型经典抗叶酸剂,其抗肿瘤活性可能来自其多谷氨酸化代谢物对几种关键叶酸需求酶同时和多重抑制。Pemetrexed 是已知的 FPGS 酶最佳底物之一(Km=1.6 μM 和 Vmax/Km=621)。Pemetrexed 的多谷氨酸化和多谷氨酸化代谢物可能在决定这种新型药物的选择性和抗肿瘤活性方面发挥着重要作用。 Pemetrexed 仅适度抑制 TS(Ki=340 nM,重组小鼠),而 Pemetrexed 的五谷氨酸的效力却是 TS 的 100 倍(Ki=3.4 nM),这使得 Pemetrexed 成为最有效的叶酸类 TS 抑制剂之一[1]

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    体内研究
    (In Vivo)

    接受 PC61 加 Pemetrexed 治疗的小鼠组在统计学上比其他组存活时间更长。在生存分析中,接受 PC61 加 Pemetrexed 治疗的小鼠组的存活时间明显长于仅接受 PC61 治疗、大鼠 IgG 加 Pemetrexed 治疗或未接受治疗的小鼠[2]

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    Clinical Trial
    分子量

    427.41

    Formula

    C20H21N5O6

    CAS 号
    性状

    固体

    颜色

    White to off-white

    中文名称

    培美曲塞

    运输条件

    Room temperature in continental US; may vary elsewhere.

    储存方式
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 6 months
    -20°C 1 month
    溶解性数据
    细胞实验: 

    DMSO 中的溶解度 : 250 mg/mL (584.92 mM; 超声助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

    H2O 中的溶解度 : < 0.1 mg/mL (insoluble)

    配制储备液
    浓度 溶剂体积 质量 1 mg 5 mg 10 mg
    1 mM 2.3397 mL 11.6984 mL 23.3967 mL
    5 mM 0.4679 mL 2.3397 mL 4.6793 mL
    查看完整储备液配制表

    * 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
    储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

    • 摩尔计算器

    • 稀释计算器

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    质量
    =
    浓度
    ×
    体积
    ×
    分子量 *

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    浓度 (start)

    C1

    ×
    体积 (start)

    V1

    =
    浓度 (final)

    C2

    ×
    体积 (final)

    V2

    动物实验:

    请根据您的 实验动物和给药方式 选择适当的溶解方案。

    以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
    ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用
    以下溶剂前显示的百分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

    • 方案 一

      请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.08 mg/mL (4.87 mM); 澄清溶液

      此方案可获得 ≥ 2.08 mg/mL(饱和度未知)的澄清溶液。

      1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL

      生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。
    • 方案 二

      请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 2.08 mg/mL (4.87 mM); 澄清溶液

      此方案可获得 ≥ 2.08 mg/mL(饱和度未知)的澄清溶液。

      1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液 中,混合均匀。

      2 g SBE-β-CD(磺丁基醚 β-环糊精)粉末定容于 10 mL 的生理盐水中,完全溶解至澄清透明。

    以下溶解方案,请直接配制工作液。建议现用现配,在短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在您配制终溶液中的体积占比; 如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶。

    • 方案 一

      请依序添加每种溶剂: 50% PEG300    50% Saline

      Solubility: 20 mg/mL (46.79 mM); 悬浊液; 超声助溶

    • 方案 二

      请依序添加每种溶剂: 20% SBE-β-CD in Saline

      Solubility: 5 mg/mL (11.70 mM); 澄清溶液; 超声助溶

    动物溶解方案计算器
    请输入动物实验的基本信息:

    给药剂量

    mg/kg

    动物的平均体重

    g

    每只动物的给药体积

    μL

    动物数量

    由于实验过程有损耗,建议您多配一只动物的量
    请输入您的动物体内配方组成:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    如果您的动物是免疫缺陷鼠或者体弱鼠,建议 DMSO 中的在最后工作液体系中的占比尽量不超过 2%。
    方案所需 助溶剂 包括:DMSO ,均可在 MCE 网站选购。 Tween 80,均可在 MCE 网站选购。
    计算结果
    工作液所需浓度 : mg/mL
    储备液配制方法 : mg 药物溶于 μL  DMSO(母液浓度为 mg/mL)。
    您所需的储备液浓度超过该产品的实测溶解度,以下方案仅供参考,如有需要,请与 MCE 中国技术支持联系。
    动物实验体内工作液的配制方法 : 取 μL DMSO 储备液,加入 μL  μL ,混合均匀至澄清,再加 μL Tween 80,混合均匀至澄清,再加 μL 生理盐水
    连续给药周期超过半月以上,请谨慎选择该方案。
    请确保第一步储备液溶解至澄清状态,从左到右依次添加助溶剂。您可采用超声加热 (超声清洗仪,建议频次 20-40 kHz),涡旋吹打等方式辅助溶解。
    纯度 & 产品资料

    纯度: 99.95%

    参考文献
    Kinase Assay
    [1]

    AICARFT inhibition assays are carried out at room temperature by monitoring the formation of [6S]-5,6,7,8-tetrahydrofolate from 10-formyl-[6R,S]-5,6,7,8-tetrahydrofolate at A298. All solutions are purged with N2 gas prior to use. The reaction solution contains 33 mM Tris-Cl, pH 7.4, 25 mM KCl, 5 mM 2-Mercaptoethanol, 0.05 mM AICA ribonucleotide, and 16 nM (2 milliunits/mL) of AICARFT. 10-Formyl-[6R,S]-5,6,7,8-tetrahydrofolate concentrations of 0.037, 0.074, and 0.145 mM are used (0.61, 1.23, and 2.45 times its Km value, respectively). LY231514 is tested as an inhibitor at 0.08-0.8 mM (four concentrations). When the tri- and pentaglutamates of LY231514 are used as inhibitors, the concentrations are 0.0005-0.009 mM (eight concentrations). Enzyme assays are initiated by the addition of enzyme. Data is analyzed using the ENZFITTER program for competitive inhibition.

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    Cell Assay
    [1]

    Dose-response curves are generated to determine the concentration required for 50% inhibition of growth (IC50). Pemetrexed is dissolved initially in DMSO at a concentration of 4 mg/mL and further diluted with cell culture medium to the desired concentration. CCRF-CEM leukemia cells in complete medium are added to 24-well Cluster plates at a final concentration of 4.8×104 cells/well in a total volume of 2 mL. Test compounds at various concentrations are added to duplicate wells so that the final volume of DMSO is 0.5%. The plates are incubated for 72 h at 37°C in an atmosphere of 5% CO2 in air. At the end of the incubation, cell numbers are determined on a ZBI Coulter counter. Control wells usually contain 4×105 to 6×105 cells at the end of the incubation. For several studies, IC50s are determined for each compound in the presence of either 300 μM AICA, 5 μM thymidine, 100 μM hypoxanthine, or combination of 5 μM hymidine plus 100 μM hypoxanthine[1].

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    Animal Administration
    [2]

    Mice[2]
    Female CBA mice and female NOD/SCID mice (NOD.CB17-Prkdcscid) at 6-8 wk of age are used. Premetrexed (100 mg/kg) is given i.p. from days 4-8 (5 consecutive d) to tumor-bearing mice to explore the synergistic effect when combined with anti-CD25 Ab or IgG control. The dose and schedule used for Pemetrexed in the current study is determined based on previous studies in mice.

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    参考文献

    完整储备液配制表

    * 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
    储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

    可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 2.3397 mL 11.6984 mL 23.3967 mL 58.4918 mL
    5 mM 0.4679 mL 2.3397 mL 4.6793 mL 11.6984 mL
    10 mM 0.2340 mL 1.1698 mL 2.3397 mL 5.8492 mL
    15 mM 0.1560 mL 0.7799 mL 1.5598 mL 3.8995 mL
    20 mM 0.1170 mL 0.5849 mL 1.1698 mL 2.9246 mL
    25 mM 0.0936 mL 0.4679 mL 0.9359 mL 2.3397 mL
    30 mM 0.0780 mL 0.3899 mL 0.7799 mL 1.9497 mL
    40 mM 0.0585 mL 0.2925 mL 0.5849 mL 1.4623 mL
    50 mM 0.0468 mL 0.2340 mL 0.4679 mL 1.1698 mL
    60 mM 0.0390 mL 0.1950 mL 0.3899 mL 0.9749 mL
    80 mM 0.0292 mL 0.1462 mL 0.2925 mL 0.7311 mL
    100 mM 0.0234 mL 0.1170 mL 0.2340 mL 0.5849 mL
    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    产品名称:
    Pemetrexed
    目录号:
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