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Merck
CN

A254

AIDA

solid

Synonym(s):

1-Amino-2,3-dihydro-1H-indene-1,5-dicarboxylic acid, 1-Aminoindan-1, 5-dicarboxylic acid, UPF 523

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About This Item

Empirical Formula (Hill Notation):
C11H11NO4
CAS Number:
168560-79-0
Molecular Weight:
221.21
NACRES:
NA.32
PubChem Substance ID:
24277957
UNSPSC Code:
12352200
MDL number:
MFCD00672638

Key Documents

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Product Name

AIDA, solid

InChI

1S/C11H11NO4/c12-11(10(15)16)4-3-6-5-7(9(13)14)1-2-8(6)11/h1-2,5H,3-4,12H2,(H,13,14)(H,15,16)

SMILES string

NC1(CCc2cc(ccc12)C(O)=O)C(O)=O

InChI key

LSTPKMWNRWCNLS-UHFFFAOYSA-N

form

solid

color

white

solubility

DMSO: 2 mg/mL

Quality Level

100

Gene Information

human ... GRM1(2911)
rat ... Grm1(24414)

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Biochem/physiol Actions

Selective mGluR1 metabotropic glutamate receptor antagonist.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
110K4605
035K4711
040K4603

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F Moroni et al.
The Journal of pharmacology and experimental therapeutics, 281(2), 721-729 (1997-05-01)
We examined the pharmacological profile of 1-aminoindan-1,5-dicarboxylic acid (AIDA), a rigid (carboxyphenyl)glycine derivative acting on metabotropic glutamate receptors (mGluRs). In cells transfected with mGluR1a, AIDA competitively antagonized the stimulatory responses of glutamate and (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid [(1S,3R)-ACPD] on phosphoinositide hydrolysis (pA2
Friedrich-Christian Deuschle et al.
Theranostics, 10(5), 2172-2187 (2020-02-25)
Enhanced amino acid supply and dysregulated integrin signaling constitute two hallmarks of cancer and are pivotal for metastatic transformation of cells. In line with its function at the crossroads of both processes, overexpression of CD98hc is clinically observed in various
Maria Joseph et al.
Molecular neurodegeneration, 12(1), 88-88 (2017-12-06)
The microtubule-associated protein Tau plays a role in neurodegeneration as well as neurogenesis. Previous work has shown that the expression of the pro-aggregant mutant Tau repeat domain causes strong aggregation and pronounced neuronal loss in the hippocampus whereas the anti-aggregant
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