KYNA Derivatives with Modified Skeleton; Hydroxyquinolines with Potential Neuroprotective Effect

Kynurenic acid (KYNA) is an endogenous neuroprotective agent of increasing importance. Several derivatives have already been synthesized, bearing an abundance of functional groups attached to the main skeleton in different positions. Several of these compounds have already been tested in biological...

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Main Authors: Bálint Lőrinczi, István Szatmári
Format: Article
Language:English
Published: MDPI AG 2021-11-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/21/11935
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author Bálint Lőrinczi
István Szatmári
author_facet Bálint Lőrinczi
István Szatmári
author_sort Bálint Lőrinczi
collection DOAJ
description Kynurenic acid (KYNA) is an endogenous neuroprotective agent of increasing importance. Several derivatives have already been synthesized, bearing an abundance of functional groups attached to the main skeleton in different positions. Several of these compounds have already been tested in biological evaluations, with several of them targeting the same receptors and biological effects as KYNA. However, these modified compounds build upon the unmodified KYNA skeleton leaving a possible route for the synthesis of new, potentially neuroprotective derivatives with heteroatom-containing ring systems. The aim of this review is to summarize the syntheses of KYNA derivatives with altered skeletons and to pinpoint an appealing transformation for future medicinal lead molecules.
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spelling doaj.art-813664015e134dd785086567adaecee02023-11-22T21:00:10ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-11-0122211193510.3390/ijms222111935KYNA Derivatives with Modified Skeleton; Hydroxyquinolines with Potential Neuroprotective EffectBálint Lőrinczi0István Szatmári1Institute of Pharmaceutical Chemistry, University of Szeged, Eötvös u. 6, H-6720 Szeged, HungaryInstitute of Pharmaceutical Chemistry, University of Szeged, Eötvös u. 6, H-6720 Szeged, HungaryKynurenic acid (KYNA) is an endogenous neuroprotective agent of increasing importance. Several derivatives have already been synthesized, bearing an abundance of functional groups attached to the main skeleton in different positions. Several of these compounds have already been tested in biological evaluations, with several of them targeting the same receptors and biological effects as KYNA. However, these modified compounds build upon the unmodified KYNA skeleton leaving a possible route for the synthesis of new, potentially neuroprotective derivatives with heteroatom-containing ring systems. The aim of this review is to summarize the syntheses of KYNA derivatives with altered skeletons and to pinpoint an appealing transformation for future medicinal lead molecules.https://www.mdpi.com/1422-0067/22/21/11935kynurenic acidmodified hydroxyquinolinesConrad–Limpach reactionneuroprotectionmodified Mannich reaction
spellingShingle Bálint Lőrinczi
István Szatmári
KYNA Derivatives with Modified Skeleton; Hydroxyquinolines with Potential Neuroprotective Effect
International Journal of Molecular Sciences
kynurenic acid
modified hydroxyquinolines
Conrad–Limpach reaction
neuroprotection
modified Mannich reaction
title KYNA Derivatives with Modified Skeleton; Hydroxyquinolines with Potential Neuroprotective Effect
title_full KYNA Derivatives with Modified Skeleton; Hydroxyquinolines with Potential Neuroprotective Effect
title_fullStr KYNA Derivatives with Modified Skeleton; Hydroxyquinolines with Potential Neuroprotective Effect
title_full_unstemmed KYNA Derivatives with Modified Skeleton; Hydroxyquinolines with Potential Neuroprotective Effect
title_short KYNA Derivatives with Modified Skeleton; Hydroxyquinolines with Potential Neuroprotective Effect
title_sort kyna derivatives with modified skeleton hydroxyquinolines with potential neuroprotective effect
topic kynurenic acid
modified hydroxyquinolines
Conrad–Limpach reaction
neuroprotection
modified Mannich reaction
url https://www.mdpi.com/1422-0067/22/21/11935
work_keys_str_mv AT balintlorinczi kynaderivativeswithmodifiedskeletonhydroxyquinolineswithpotentialneuroprotectiveeffect
AT istvanszatmari kynaderivativeswithmodifiedskeletonhydroxyquinolineswithpotentialneuroprotectiveeffect