Kainic acid monohydrate
SIGMA/K0250 - ≥99% (TLC)
Synonym: Digenin, Kainate; 2-
CAS Number: 58002-62-3
Empirical Formula (Hill Notation): C10H15NO4 · H2O
Molecular Weight: 231.25
MDL Number: MFCD00150833
Linear Formula: C10H15NO4 · H2O
Product Type: Chemical
| assay | ≥99% (TLC) |
| form | powder |
| impurities | Glutamate, free |
| InChI | 1S/C10H15NO4.H2O/c1-5(2)7 |
| InChI key | FZNZRJRSYLQHLT-SLGZUKMRSA |
| Quality Level | 100 ![]() |
| SMILES string | O.CC(=C)[C@H]1CN[C@@H]([C |
| solubility | H2O: soluble |
| storage temp. | 2-8°C |
| Application: | Kainic acid (KA) has been used: • tostudy mechanisms of excitation-induced apoptosis and epilepsy. • to hamper themitochondrial function () • used to induce c-fosexpression in the mice′s brains, specifically targeting the dorsal hippocampus.() |
| Biochem/physiol Actions: | Agonist for kainate class of ionotropic glutamate receptors. |
| Biochem/physiol Actions: | Kainic acid monohydrate disrupts mitochondrial function by inducing the release of lactate dehydrogenase (LDH) and reducing 3-(4,5-dimethylthiazole-2 |
| Biochem/physiol Actions: | Kainic acid monohydrate is an agonist at the kainate class of ionotropic glutamate receptors, which induces seizures and neurodegeneration in vivo and is used to induce experimental epilepsy in rodents and study the mechanisms of excitation-induced neuronal apoptosis. |
| Features and Benefits: | This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm . |
| Features and Benefits: | This compound is featured on the Excitatory Amino Acid Transporters and Glutamate Receptors (Ion Channel Family) pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here . |
| General description: | Kainic acid monohydrate serves as an agonist for kainate-class ionotropic glutamate receptors, initiating seizures and neurodegeneration in live organisms. It is employed to induce experimental epilepsy in rodents and to explore the mechanisms underlying excitation-induced neuronal apoptosis. |
| Packaging: | 10, 50 mg in glass insert |
| Preparation Note: | Dissolve in 1-2 drops of 1N NaOH then bring to volume with water or aqueous buffer. Can be stored 1-2 days refrigerated. |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | ≥99% (TLC) |
| Storage Temp. | 2-8°C |
| UNSPSC | 12352106 |

