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| Product | Description | |
|---|---|---|
| (RS)-3,5-DHPG | (RS)-3,5-DHPG. Group: Biochemicals. Grades: Purified. CAS No. 19641-83-9. Pack Sizes: 1mg, 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| (RS)-3,5-DHPG | (RS)-3,5-DHPG is a group I metabotropic glutamate receptor (mGluR) agonist with selectivity for both mGlu1 and mGlu5. It is also acts as an antagonist at metabotropic glutamate receptors linked to phospholipase D. Synonyms: (RS)-3,5-Dihydroxyphenylglycine; α-Amino-3,5-dihydroxybenzeneacetic Acid; (±)-α-Amino-3,5-dihydroxybenzeneacetic Acid; 3,5-Dihydroxyphenylglycine; DL-2-(3,5-Dihydroxyphenyl)glycine. Grades: ≥99% by HPLC. CAS No. 19641-83-9. Molecular formula: C8H9NO4. Mole weight: 183.16. |  |
| DHPG | DHPG ((RS)-3,5-DHPG) is an amino acid, which acts as a selective and potent agonist of group I mGluR (mGluR 1 and mGluR 5), shows no effect on Group II or Group III mGluRs [1]. DHPG ((RS)-3,5-DHPG) is also an effective antagonist of mGluRs linked to phospholipase D [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (RS)-3,5-DHPG. CAS No. 146255-66-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-12598A. |  |
| ω-Conotoxin GVIA | ω-Conotoxin GVIA is a peptide neurotoxin first isolated from the marine snail Conus geographus L. It selectively and reversibly blocks specific voltage-dependent N-type Ca2+ channels in neurons, but not in muscle. It reduces (RS)-3,5-DHPG2-induced long term depression in vivo. It does not bind to either the dihydropyridine or verapamil binding sites. It is used as a powerful probe for exploring the vertebrate pre-synaptic terminal. Synonyms: omega-Conotoxin gvia. CAS No. 106375-28-4. Molecular formula: C120H182N38O43S6. Mole weight: 3037.34. | |
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