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Homoquinolinic acid

Homoquinolinic acid (HQA) is a potent excitotoxin[1] which is a conformationally-restricted analogue of N-methyl-D-aspartate (NMDA) and a partial agonist of the main/glutamate site of the NMDA receptor, with some selectivity for NR2B subunit-containing receptors.[2][3][4] It is approximately equipotent to NMDA and about five times more potent than quinolinic acid as an agonist of the NMDA receptor.[5] HQA has also been found to label a novel, yet uncharacterized binding site, which can be distinguished from the NMDA receptor with the use of 2-carboxy-3-carboxymethylquinoline (CCMQ), a selective ligand of the uncharacterized site.[6]

Homoquinolinic acid
Clinical data
Other namesHomoquinolinate
ATC code
  • None
Identifiers
  • 3-(Carboxymethyl)-2-pyridinecarboxylic acid
CAS Number
  • 490-75-5
PubChem CID
  • 3080554
ChemSpider
  • 2338312
PDB ligand
  • QM1 (PDBe, RCSB PDB)
CompTox Dashboard (EPA)
  • DTXSID70197658
ECHA InfoCard100.164.902
Chemical and physical data
FormulaC8H7NO4
Molar mass181.147 g·mol−1
3D model (JSmol)
  • Interactive image
  • c1cc(c(nc1)C(=O)O)CC(=O)O
  • InChI=1S/C8H7NO4/c10-6(11)4-5-2-1-3-9-7(5)8(12)13/h1-3H,4H2,(H,10,11)(H,12,13)
  • Key:HQPMJFFEXJELOQ-UHFFFAOYSA-N

See also edit

References edit

  1. ^ Stone TW (1989). Quinolinic acid and the kynurenines. CRC Press. ISBN 978-0-8493-6592-8.
  2. ^ Stolerman IP (31 July 2010). Encyclopedia of Psychopharmacology. Springer Science & Business Media. pp. 511–. ISBN 978-3-540-68698-9.
  3. ^ de Carvalho LP, Bochet P, Rossier J (April 1996). "The endogenous agonist quinolinic acid and the non endogenous homoquinolinic acid discriminate between NMDAR2 receptor subunits". Neurochemistry International. 28 (4): 445–52. doi:10.1016/0197-0186(95)00091-7. PMID 8740453. S2CID 19395334.
  4. ^ Lemke TL, Williams DA (24 January 2012). Foye's Principles of Medicinal Chemistry. Lippincott Williams & Wilkins. pp. 404–. ISBN 978-1-60913-345-0.
  5. ^ C.S.A. Neurosciences Abstracts. Cambridge Scientific Abstracts. 1984.
  6. ^ Egebjerg J, Schousboe A, Krogsgaard-Larsen P (4 October 2001). Glutamate and GABA Receptors and Transporters: Structure, Function and Pharmacology. CRC Press. pp. 73–. ISBN 978-0-203-29938-8.

homoquinolinic, acid, potent, excitotoxin, which, conformationally, restricted, analogue, methyl, aspartate, nmda, partial, agonist, main, glutamate, site, nmda, receptor, with, some, selectivity, nr2b, subunit, containing, receptors, approximately, equipotent. Homoquinolinic acid HQA is a potent excitotoxin 1 which is a conformationally restricted analogue of N methyl D aspartate NMDA and a partial agonist of the main glutamate site of the NMDA receptor with some selectivity for NR2B subunit containing receptors 2 3 4 It is approximately equipotent to NMDA and about five times more potent than quinolinic acid as an agonist of the NMDA receptor 5 HQA has also been found to label a novel yet uncharacterized binding site which can be distinguished from the NMDA receptor with the use of 2 carboxy 3 carboxymethylquinoline CCMQ a selective ligand of the uncharacterized site 6 Homoquinolinic acidClinical dataOther namesHomoquinolinateATC codeNoneIdentifiersIUPAC name 3 Carboxymethyl 2 pyridinecarboxylic acidCAS Number490 75 5PubChem CID3080554ChemSpider2338312PDB ligandQM1 PDBe RCSB PDB CompTox Dashboard EPA DTXSID70197658ECHA InfoCard100 164 902Chemical and physical dataFormulaC 8H 7N O 4Molar mass181 147 g mol 13D model JSmol Interactive imageSMILES c1cc c nc1 C O O CC O OInChI InChI 1S C8H7NO4 c10 6 11 4 5 2 1 3 9 7 5 8 12 13 h1 3H 4H2 H 10 11 H 12 13 Key HQPMJFFEXJELOQ UHFFFAOYSA NSee also editAspartate Ibotenic acid TetrazolylglycineReferences edit Stone TW 1989 Quinolinic acid and the kynurenines CRC Press ISBN 978 0 8493 6592 8 Stolerman IP 31 July 2010 Encyclopedia of Psychopharmacology Springer Science amp Business Media pp 511 ISBN 978 3 540 68698 9 de Carvalho LP Bochet P Rossier J April 1996 The endogenous agonist quinolinic acid and the non endogenous homoquinolinic acid discriminate between NMDAR2 receptor subunits Neurochemistry International 28 4 445 52 doi 10 1016 0197 0186 95 00091 7 PMID 8740453 S2CID 19395334 Lemke TL Williams DA 24 January 2012 Foye s Principles of Medicinal Chemistry Lippincott Williams amp Wilkins pp 404 ISBN 978 1 60913 345 0 C S A Neurosciences Abstracts Cambridge Scientific Abstracts 1984 Egebjerg J Schousboe A Krogsgaard Larsen P 4 October 2001 Glutamate and GABA Receptors and Transporters Structure Function and Pharmacology CRC Press pp 73 ISBN 978 0 203 29938 8 nbsp This drug article relating to the nervous system is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Homoquinolinic acid amp oldid 1135331917, wikipedia, wiki, book, books, library,

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