α-Guanidinoglutaric Acid
CAS No. 73477-53-9
α-Guanidinoglutaric Acid ( —— )
Catalog No. M27423 CAS No. 73477-53-9
α-Guanidinoglutaric Acid is found in cobalt-induced epileptogenic focus tissue in the cerebral cortex of cats.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 45 | Get Quote |
|
5MG | 53 | Get Quote |
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10MG | 76 | Get Quote |
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25MG | 133 | Get Quote |
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50MG | 194 | Get Quote |
|
100MG | 334 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product Nameα-Guanidinoglutaric Acid
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NoteResearch use only, not for human use.
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Brief Descriptionα-Guanidinoglutaric Acid is found in cobalt-induced epileptogenic focus tissue in the cerebral cortex of cats.
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Descriptionα-Guanidinoglutaric Acid is found in cobalt-induced epileptogenic focus tissue in the cerebral cortex of cats. α-Guanidinoglutaric Acid-induced seizures are associated with abnormal serotonergic function and that they are initiated by a decrease in the 5-HT level.(In Vivo):α-Guanidinoglutaric Acid induced epileptic seizures in rats after intraventricular administration. Sporadic low-voltage spikes appeared 4 min after the administration of α-Guanidinoglutaric Acid. Spikes increased in voltage 6 min after the administration. Multiple spikes appeared 10 min after the administration, and they reached maximal frequency 30 min after the administration. The epileptic discharges disappeared 100 min after the administration. The 5-HT level increased in the right and left cortices 3 min after the administration. The 5-HT level decreased in the mid-brain 5 min after the administration and subsequently in all regions of the brain 10 min after the administration. No change in the 5-HT level was found 30 min and 100 min after the administration.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorPTK
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Research Area——
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Indication——
Chemical Information
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CAS Number73477-53-9
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Formula Weight189.2
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Molecular FormulaC6H11N3O4
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Purity>98% (HPLC)
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Solubility——
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SMILESNN=CN[C@@H](CCC(O)=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
1.Dou DQ, et al. The inhibitory effects of ginsenosides on protein tyrosine kinase activated by hypoxia/reoxygenation in cultured human umbilical vein endothelial cells. Planta Med. 2001 Feb;67(1):19-23.
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