U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C18H12Cl2N2O3
Molecular Weight 375.205
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of GAVESTINEL

SMILES

OC(=O)C1=C(\C=C\C(=O)NC2=CC=CC=C2)C3=C(Cl)C=C(Cl)C=C3N1

InChI

InChIKey=WZBNEZWCNKUOSM-VOTSOKGWSA-N
InChI=1S/C18H12Cl2N2O3/c19-10-8-13(20)16-12(17(18(24)25)22-14(16)9-10)6-7-15(23)21-11-4-2-1-3-5-11/h1-9,22H,(H,21,23)(H,24,25)/b7-6+

HIDE SMILES / InChI

Molecular Formula C18H12Cl2N2O3
Molecular Weight 375.205
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Description

GV 150526A (gavestinel) is an investigational drug for a neuroprotective therapy of acute ischemic stroke within 6 hours of symptom onset. It is a potent and selective non-competitive antagonist at the glycine site of the N-methyl-D-aspartate receptor (NMDA) which reduces infarct volume in experimental stroke models. Gavestinel acts at the strychnine-insensitive glycine binding site of the NMDA receptor-channel complex with nanomolar affinity (pKi = 8.5), coupled with high glutamate receptor selectivity. Gavestinel displays higher than 1000-fold selectivity over NMDA, AMPA and kainate binding sites and is orally bioavailable and active in vivo. GV 150526A inhibited convulsions induced by NMDA in mice, when administered by both IV and po routes (ED50 = 0.06 and 6 mg/kg, respectively). The safety and efficacy of GV150526 were studied in two phase III randomized placebo-controlled clinical trials of acute ischemic stroke patients within 6 h from onset [The Glycine Antagonist in Neuroprotection (GAIN) International and GAIN Americas Trials] sponsored by GlaxoSmithKline. The results of these trials suggested that gavestinel was not of substantial benefit or harm to patients with primary intracerebral hemorrhage.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
8.5 null [pKi]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Cmax

ValueDoseCo-administeredAnalytePopulation
135 μg/mL
400 mg 2 times / day steady-state, intravenous
GV 150526A plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
55.9 h
400 mg 2 times / day steady-state, intravenous
GV 150526A plasma
Homo sapiens

Funbound

ValueDoseCo-administeredAnalytePopulation
3.6%
400 mg 2 times / day steady-state, intravenous
GV 150526A plasma
Homo sapiens

Drug as perpetrator​

Drug as victim

PubMed

Sample Use Guides

In Vivo Use Guide
Gavestinel loading dose of 800 mg plus 5 maintenance doses (200 mg every 12 hours) for 3 days.
Route of Administration: Intravenous
In Vitro Use Guide
The effect of selective antagonist GV 150526A at trychnine-insensitive glycine sites was studied by measuring how much glycine potentiated the [3H]dopamine and [3H]noradrenaline release induced by 100 uM N-methyl-D-aspartate (NMDA) from superfused striatal and hippocampal synaptosomes in a Mg2+-free buffer. GV 150526A inhibited the effect of NMDA alone and potently antagonized the effect of glycine, with Ki = 12.4 and 17.3 nM for [3H]dopamine and [3H]noradrenaline release.
Substance Class Chemical
Record UNII
318X4QY113
Record Status Validated (UNII)
Record Version