Английская Википедия:DNI-Glutamate

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Версия от 21:50, 23 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{chembox |Verifiedfields=changed |Watchedfields=changed |verifiedrevid=458976435 |ImageFile=DNI-Glutamate.png |ImageSize1= |IUPACName=2-amino-5-(4-methoxy-5,7-dinitroindolin-1-yl)-5-oxopentanoic acid |OtherNames=DNI-Glu<br/>Dinitroindoline-glutamate<br/>DMNI-Glu |Section1={{Chembox Identifiers | CASNo = 864085-92-7 | ChemSpiderID = 29321113 | PubChem = 124221751 | StdInChI=1S/C14H16N4...»)
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Шаблон:Chembox

DNI-Glutamate ((S)-α-Amino-2,3-dihydro-4-methoxy-5,7-dinitro-δ-oxo-1H-indole-1-pentanoic acid) is a caged form of the glutamate neurotransmitter, which is photocleavable by one- (lexc = 360 nm) as well as two-photon irradiation (lexc = 720 nm). Upon photocleaveage, the bioactive glutamate is released instantly and behaves as a neurotransmitter, which provides information about receptor distribution, channel kinetics and network circuitry of the neuronal network.[1] DNI-Glu is an analogue of the common MNI-Glu compound, but it exhibits cca. 7-10 times larger efficiency in terms of quantum yields compared to the MNI compound. DNI-Glu has low biotoxicity and high water-solubility as well (at physiologic pH).[1] Due to these properties, currently DNI-Glu is thought to be the most advanced caged-glutamate compound for neuroscientific research.

Discovery

DNI-Glu, the molecule itself was first discovered by George Papageorgiou in 2005,[2] but its practical implementation was not mentioned in his publications.  Later, in 2009, the compound was reinvestigated in neurophysiological studies and its high efficacy and beneficial properties were reported. The product is commercially available as a trifluoroacetate salt of the compound which was proved to be much more stable and less hygroscopic.[1]

References

Шаблон:Reflist