CGP-35348: Difference between revisions
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| verifiedrevid = |
| verifiedrevid = 438956231 |
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| IUPAC_name = 3-aminopropyl(diethoxymethyl)phosphinic acid |
| IUPAC_name = 3-aminopropyl(diethoxymethyl)phosphinic acid |
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| image = CGP-35348_structure.png |
| image = CGP-35348_structure.png |
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| ATC_supplemental = |
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| PubChem = 107699 |
| PubChem = 107699 |
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| chemical_formula = |
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Revision as of 19:10, 10 September 2011
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| Chemical and physical data | |
| Formula | C8H20NO4P |
| Molar mass | 225.222 g/mol g·mol−1 |
| 3D model (JSmol) | |
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CGP-35348 is a compound used in scientific research which acts as an antagonist at GABAB receptors.[1][2][3]
References
- ^ Carter LP, Chen W, Coop A, Koek W, France CP (2006). "Discriminative stimulus effects of GHB and GABA(B) agonists are differentially attenuated by CGP35348". European Journal of Pharmacology. 538 (1–3): 85–93. doi:10.1016/j.ejphar.2006.03.039. PMID 16647701.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ Nasrallah FA, Griffin JL, Balcar VJ, Rae C (2007). "Understanding your inhibitions: modulation of brain cortical metabolism by GABA(B) receptors". Journal of Cerebral Blood Flow and Metabolism. 27 (8): 1510–20. doi:10.1038/sj.jcbfm.9600453. PMID 17293844.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ Koek W, Mercer SL, Coop A, France CP (2009). "Behavioral effects of gamma-hydroxybutyrate, its precursor gamma-butyrolactone, and GABA(B) receptor agonists: time course and differential antagonism by the GABA(B) receptor antagonist 3-aminopropyl(diethoxymethyl)phosphinic acid (CGP35348)". The Journal of Pharmacology and Experimental Therapeutics. 330 (3): 876–83. doi:10.1124/jpet.109.151845. PMID 19564487.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link)
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