Talampanel - ≥98%(HPLC), high purity , Glutamate receptor ionotropic, AMPA 1 antagonist, CAS No.161832-65-1, Glutamate receptor ionotropic, AMPA 1 antagonist

Item Number
T287576
Grouped product items
SKUSizeAvailabilityPrice Qty
T287576-10mg
10mg
Available within 8-12 weeks(?)
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$155.90

Non-competitive non-NMDA iGluR antagonist

View related series
GluA2 Antagonist

Basic Description

SynonymsTalampanel | 161832-65-1 | Ampanel | GYKI 53773 | Kinampa | LY-300164 | GYKI-53773 | LY 300164 | Talampanel (INN) | Talampanel [INN] | (-)-Talampanel | (8R)-7-acetyl-5-(4-aminophenyl)-8,9-dihydro-8-methyl-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine | LY300164 | 1-[(8R)-5-(4-aminophen
Specifications & PurityMoligand™, ≥98%(HPLC)
Biochemical and Physiological MechanismsNon-competitive AMPA/kainate receptor antagonist that displays 2.3-3-fold more potent activity thanGYKI 52466. Potentiates the anticonvulsive activity of antiepileptic drugs in animal models of seizures. Orally active.
Storage TempStore at 2-8°C
Shipped InWet ice
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionGlutamate receptor ionotropic, AMPA 1 antagonist

Product Properties

ALogP2.7

Associated Targets(Human)

GRIA2 Tclin Glutamate receptor 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gallus gallus (1187 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meriones unguiculatus (417 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name 1-[(8R)-5-(4-aminophenyl)-8-methyl-8,9-dihydro-[1,3]dioxolo[4,5-h][2,3]benzodiazepin-7-yl]ethanone
INCHI InChI=1S/C19H19N3O3/c1-11-7-14-8-17-18(25-10-24-17)9-16(14)19(21-22(11)12(2)23)13-3-5-15(20)6-4-13/h3-6,8-9,11H,7,10,20H2,1-2H3/t11-/m1/s1
InChi Key JACAAXNEHGBPOQ-LLVKDONJSA-N
Canonical SMILES CC1CC2=CC3=C(C=C2C(=NN1C(=O)C)C4=CC=C(C=C4)N)OCO3
Isomeric SMILES C[C@@H]1CC2=CC3=C(C=C2C(=NN1C(=O)C)C4=CC=C(C=C4)N)OCO3
WGK Germany 3
PubChem CID 164509
Molecular Weight 337.37

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySolvent:DMSO, Max Conc. mg/mL: 33.74, Max Conc. mM: 100

Safety and Hazards(GHS)

Pictogram(s) GHS06,   GHS09
Signal Danger
Hazard Statements

H301:Toxic if swallowed

H400:Very toxic to aquatic life

H410:Very toxic to aquatic life with long lasting effects

Precautionary Statements

P273:Avoid release to the environment.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P391:Collect spillage.

P330:Rinse mouth.

P301+P316:IF SWALLOWED: Get emergency medical help immediately.

WGK Germany 3
RIDADR UN2811-class6.1-PG3-EHS-Toxicsolids,organic,n.o.s.,HI:all

Related Documents

References

1. Aujla PK, Fetell MR, Jensen FE.  (2009)  Talampanel suppresses the acute and chronic effects of seizures in a rodent neonatal seizure model..  Epilepsia,  50  (4): (694-701).  [PMID:19220413]
2. Wang C, Niu L.  (2013)  Mechanism of inhibition of the GluA2 AMPA receptor channel opening by talampanel and its enantiomer: the stereochemistry of the 4-methyl group on the diazepine ring of 2,3-benzodiazepine derivatives..  ACS Chem Neurosci,  (4): (635-44).  [PMID:23402301]

Solution Calculators