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How to Cite 1. For In-Text Citation (Materials & Methods): 2. For Key Resources Table: |
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| Formula | C20H21N5O6.7H2O.2Na |
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| Molecular Weight | 599.50 | CAS No. | 357166-29-1 | ||||
| Solubility (25°C)* | In vitro | Water | 100 mg/mL (166.8 mM) | ||||
| DMSO | 33 mg/mL (55.04 mM) | ||||||
| Ethanol | Insoluble | ||||||
| In vivo (Add solvents to the product individually and in order) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
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| Description | Pemetrexed (disodium heptahydrate) is a folate antimetabolite that inhibits thymidylate synthase, dihydrofolate reductase and glycinamide ribonucleotide formyltransferase. It also induces apoptosis and cell-cycle arrest in non-small-cell lung cancer carrying an EGFR exon 19 deletion. | ||
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| Baicalin Regulates Proliferation, Apoptosis, Migration, and Invasion in Mesothelioma [ Medical Science Monitor, October 31, 2019, 8172-8180] | PubMed: 31670317 |
| Decitabine Sensitizes the Radioresistant Lung Adenocarcinoma to Pemetrexed Through Upregulation of Folate Receptor Alpha [ Frontiers in Oncology, May 17, 2021, 668798] | PubMed: 34079760 |
| A Novel Molecular Target in EGFR-mutant Lung Cancer Treated With the Combination of Osimertinib and Pemetrexed [ Anticancer Research, 2022, 709-722] | PubMed: 35093869 |
| Upregulation of Thymidylate Synthase Induces Pemetrexed Resistance in Malignant Pleural Mesothelioma [ Frontiers in Pharmacology, 2021, 718675] | PubMed: 34646134 |
| [pemetrexed + sildenafil], via autophagy-dependent HDAC downregulation, enhances the immunotherapy response of NSCLC cells [ Cancer Biology & Therapy, 2017, 705-714] | PubMed: 28812434 |
| Inhibition of Wee1 sensitizes cancer cells to anti-metabolite chemotherapeutics in vitro and in vivo, independent of p53 functionality [ Molecular Cancer Therapeutics, 2013, 2675-2684] |
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