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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
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Description
Curator's Comment: Description was created using several sources including: https://www.ncbi.nlm.nih.gov/pubmed/16340185; https://www.ncbi.nlm.nih.gov/pubmed/15831831

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.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
8.5 null [pKi]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
135 μg/mL
400 mg 2 times / day steady-state, intravenous
dose: 400 mg
route of administration: Intravenous
experiment type: STEADY-STATE
co-administered:
GV 150526A plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
55.9 h
400 mg 2 times / day steady-state, intravenous
dose: 400 mg
route of administration: Intravenous
experiment type: STEADY-STATE
co-administered:
GV 150526A plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
3.6%
400 mg 2 times / day steady-state, intravenous
dose: 400 mg
route of administration: Intravenous
experiment type: STEADY-STATE
co-administered:
GV 150526A plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
OverviewDrug as perpetrator​Drug as victim
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

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
Created
by admin
on Fri Dec 15 15:25:59 GMT 2023
Edited
by admin
on Fri Dec 15 15:25:59 GMT 2023
Record UNII
318X4QY113
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GAVESTINEL
INN   MART.   USAN  
INN   USAN  
Official Name English
GAVESTINEL [MART.]
Common Name English
GV-150526X
Code English
GV 150526X
Code English
4,6-Dichloro-3-[(E)-2-(phenylcarbamoyl)vinyl]indole-2-carboxylic acid
Systematic Name English
GAVESTINEL [USAN]
Common Name English
gavestinel [INN]
Common Name English
E)-4,6-DICHLORO-3-(3-OXO-3-(PHENYLAMINO)-1-PROPENYL)-1H-INDOLE-2-CARBOXYLIC ACID
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
Code System Code Type Description
CAS
153436-22-7
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID90870012
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
MESH
C105319
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
FDA UNII
318X4QY113
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
USAN
KK-65
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
NCI_THESAURUS
C74117
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
SMS_ID
100000084537
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
DRUG BANK
DB06741
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
EVMPD
SUB07886MIG
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
WIKIPEDIA
GAVESTINEL
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
INN
7428
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
ChEMBL
CHEMBL44793
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
PUBCHEM
6450546
Created by admin on Fri Dec 15 15:25:59 GMT 2023 , Edited by admin on Fri Dec 15 15:25:59 GMT 2023
PRIMARY
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TARGET -> INHIBITOR
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ACTIVE MOIETY