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AIDA - ≥98%(HPLC), high purity , CAS No.168560-79-0, Antagonist of mGlu 1 receptor

  • Moligand™
  • ≥98%(HPLC)
Item Number
A286905
Grouped product items
SKUSizeAvailabilityPrice Qty
A286905-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$185.90
A286905-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$777.90

Potent and selective group I mGlu antagonist

View related series
mGlu1 receptor Antagonist

Basic Description

SynonymsAIDA|168560-79-0|UPF 523|1-Aminoindan-1,5-dicarboxylic acid|GNF-PF-1401|1-Amino-2,3-dihydro-1H-indene-1,5-dicarboxylic acid|UPF-523|1-amino-2,3-dihydroindene-1,5-dicarboxylic acid|1H-Indene-1,5-dicarboxylic acid, 1-amino-2,3-dihydro-|CHEMBL313938|UPF523;U
Specifications & PurityMoligand™, ≥98%(HPLC)
Biochemical and Physiological MechanismsA relatively potent and selective antagonist of group I metabotropic glutamate receptors (mGlu1a), having no effect on group II (mGlu2) or group III (mGlu4) receptors expressed individually in baby hamster kidney cells. Has no effect on ionotropic glutama
Storage TempRoom temperature
Shipped InNormal
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of mGlu 1 receptor

Associated Targets

POLB Tchem DNA polymerase beta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

POLH Tchem DNA polymerase eta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TXNRD1 Tclin Thioredoxin reductase 1, cytoplasmic 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MPHOSPH8 Tbio M-phase phosphoprotein 8 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BLM Tchem Bloom syndrome protein 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPT Tclin Microtubule-associated protein tau 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GRM1 Tchem Metabotropic glutamate receptor 1 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GRM2 Tchem Metabotropic glutamate receptor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GRM4 Tchem Metabotropic glutamate receptor 4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GRM5 Tchem Metabotropic glutamate receptor 5 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4E Tchem Lysine-specific demethylase 4E 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 1-amino-2,3-dihydroindene-1,5-dicarboxylic acid
INCHI 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)
InChi Key LSTPKMWNRWCNLS-UHFFFAOYSA-N
Canonical SMILES C1CC(C2=C1C=C(C=C2)C(=O)O)(C(=O)O)N
Isomeric SMILES C1CC(C2=C1C=C(C=C2)C(=O)O)(C(=O)O)N
PubChem CID 2071
Molecular Weight 221.21

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySolvent:1.1eq. NaOH, Max Conc. mg/mL: 22.12, Max Conc. mM: 100

Related Documents

Solution Calculators