Sodium Oxamate
CAS No. 565-73-1
Sodium Oxamate( SO, oxamate sodium, Aminooxoacetic acid sodium salt, Oxamic acid sodium salt )
Catalog No. M22595 CAS No. 565-73-1
Sodium Oxamate is an LDH inhibitor. Sodium oxamate (SO) induces G2/M cell cycle arrest via downregulation of the CDK1/cyclin B1 pathway and promotes apoptosis through enhancement of mitochondrial ROS generation.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1G | 29 | In Stock |
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Biological Information
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Product NameSodium Oxamate
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NoteResearch use only, not for human use.
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Brief DescriptionSodium Oxamate is an LDH inhibitor. Sodium oxamate (SO) induces G2/M cell cycle arrest via downregulation of the CDK1/cyclin B1 pathway and promotes apoptosis through enhancement of mitochondrial ROS generation.
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DescriptionSodium Oxamate is an LDH inhibitor. Sodium oxamate (SO) induces G2/M cell cycle arrest via downregulation of the CDK1/cyclin B1 pathway and promotes apoptosis through enhancement of mitochondrial ROS generation.It inhibits L(+)-lactate dehydrogenase and derails the entire gluconeogenic pathway.NETosis and lactate accumulation during LPS induced sepsis in mice was inhibited by sodium oxamate, LDH inhibitor.
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In VitroCell Proliferation Assay Cell Line:CNE-1 and CNE-2 cells Concentration:10 μM Incubation Time:24-72 hours Result:Showed IC50s of 74.6, 32.4 and 17.8 mM and 62.3, 44.5, 31.6 mM at 24, 48 and 72 h in the CNE-1 and CNE-2 cancer cells, respectively.Apoptosis Analysis Cell Line:NPC cells Concentration:0, 20, 50 and 100 mM Incubation Time:48 hours Result:Showed the increasement of early and late apoptotic cells in a dose-dependent manner. Increased the expression of pro-apoptotic Bax and cleaved-caspase-3, while reduced the anti-apoptotic signals of Bcl-2 and pro-caspase-3.Cell Cycle Analysis Cell Line:CNE-1 and CNE-2 cells Concentration:0, 20, 50 and 100 mM Incubation Time:24 hours Result:Showed a dose-dependent increase in the numbers of CNE-1 and CNE-2 cells in the G2/M phase.
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In VivoAnimal Model:Female Balb/c nude mice injected with CNE-1 cells Dosage:750 mg/kg Administration:Intraperitoneal injection; 750 mg/kg; once daily; 3 weeks Result:Inhibited the tumor growth when compared to either oxamate alone or irradiation alone.
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SynonymsSO, oxamate sodium, Aminooxoacetic acid sodium salt, Oxamic acid sodium salt
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PathwayApoptosis
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TargetApoptosis
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RecptorLDH|CDK|Apoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number565-73-1
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Formula Weight111.03
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Molecular FormulaC2H2NNaO3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 12.5 mg/mL (112.58 mM)
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SMILES[Na+].NC(=O)C([O-])=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Vitamin E succinate
Vitamin E succinate (D-alpha-Tocopherol Succinate) is an antioxidant tocopherol that belongs to the vitamin E class of compounds Vitamin E succinate has antitumor activity, induces apoptosis, and is used as an adjuvant in the treatment of cancer and in the synthesis of INVITE, a biocoupling compound.
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Hinokitiol
Hinokitiol (4-Isopropyltropolone;β-Thujaplicin) is a tropolone-related natural compound that can induces apoptosis and cell cycle arrest.
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(E/Z)-BCI
(E/Z)-BCI attenuates LPS-induced inflammatory mediators and ROS production in macrophage cells via activating the Nrf2 signaling axis and inhibiting the NF-κB pathway. (E/Z)-BCI is a dual-specificity phosphatase 6 (DUSP6) inhibitor with anti-inflammatory activities.
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