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(1,2,5,6-Tetrahydropyridin-4-yl)methylphosphinic acid hydrate_Molecular_structure_CAS_182485-36-5(anhydrous))
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(1,2,5,6-Tetrahydropyridin-4-yl)methylphosphinic acid hydrate

Catalog No. T200 Name Sigma Aldrich
CAS Number 182485-36-5(anhydrous) Website http://www.sigmaaldrich.com
M. F. C6H14NO3P Telephone 1-800-521-8956
M. W. 179.154021 Fax
Purity ≥97% (NMR) Email
Storage Chembase ID: 132738

SYNONYMS

IUPAC name
P-methyl-1,2,3,6-tetrahydropyridin-1-ium-4-phosphinate hydrate
IUPAC Traditional name
P-methyl-1,2,3,6-tetrahydropyridin-1-ium-4-phosphinate hydrate
Synonyms
TPMPA hydrate

DATABASE IDS

PubChem SID 24278172
CAS Number 182485-36-5(anhydrous)

PROPERTIES

Purity ≥97% (NMR)
Apperance white to off-white solid
Solubility H2O: soluble16 mg/mL
Solubility DMSO: insoluble
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Legal Information
Sold in the USA under exclusive license from the University of California.
Biochem/physiol Actions
TPMPA is a hybrid of isoguvacine and 3-APMPA designed to retain affinity for GABAC receptors but not to interact with GABAA or GABAB receptors. Electrical assays show that TPMPA is a competitive antagonist of cloned human mu 1 GABAC receptors expressed in Xenopus laevis oocytes (Kb approx. 2 μM). TPMPA is >100-fold weaker as an inhibitor of rat brain GABAA receptors expressed in oocytes (Kb approx. 320 μM) and has only weak agonist activity on GABAB receptors assayed in rat hippocampal slices (EC50 approx. 500 μM). TPMPA may be used to investigate GABAC receptor function in the outer retina and in any other areas of the nervous system in which these types of receptor are present.

REFERENCES