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Details

Stereochemistry ACHIRAL
Molecular Formula C25H24N4O2
Molecular Weight 412.4837
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of BIX-02188

SMILES

CN(C)CC1=CC(N\C(=C2/C(=O)NC3=C2C=CC(=C3)C(N)=O)C4=CC=CC=C4)=CC=C1

InChI

InChIKey=FSZPIAXLCCQFCM-FCQUAONHSA-N
InChI=1S/C25H24N4O2/c1-29(2)15-16-7-6-10-19(13-16)27-23(17-8-4-3-5-9-17)22-20-12-11-18(24(26)30)14-21(20)28-25(22)31/h3-14,27H,15H2,1-2H3,(H2,26,30)(H,28,31)/b23-22-

HIDE SMILES / InChI

Molecular Formula C25H24N4O2
Molecular Weight 412.4837
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

BIX-02188 is a selective inhibitor of MEK5 with IC50 of 4.3 nM, also inhibits ERK5 catalytic activity with IC50 of 810 nM, and does not inhibit closely related kinases MEK1, MEK2, ERK2, and JNK2. Intrathecal injection of BIX-02188, a novel specific inhibitor of mitogen-activated protein kinases kinase 5 (MEK5), produced a dose- and time-dependent inhibition of the activation of spinal ERK5, without affecting activation of other MAPKs. Moreover, selective attenuation of spinal p-ERK5 expression by BIX-02188 could significantly relieve morphine withdrawal symptom, accompanying with the decreased phosphorylation of cAMP response-element binding protein (CREB) in the spinal cord. These findings suggested that activation of the ERK5 signaling pathway might contribute to morphine physical dependence and its specific pharmacological inhibitor BIX0-2188 could be a potential therapeutic choice for alleviation of morphine withdrawal symptoms in the future.

CNS Activity

Curator's Comment: In rats centrally active in vivo

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
810.0 nM [IC50]
4.3 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
A new high resolution screening method for study of phenotype stress responses of Saccharomyces cerevisae mutants.
2011-12
Identification of pharmacological inhibitors of the MEK5/ERK5 pathway.
2008-12-05
Patents

Sample Use Guides

Rats: the reduction of p-ERK5 was detected at 30 min, and the most significant reduction was detected at 1 h after intrathecal injection of BIX-02188 (10ug).
Route of Administration: Other
Inhibition of ERK5 activation by BIX02188 (5uM) decreased the gene expression of type II collagen and aggrecan in NP cells.
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:32:03 GMT 2025
Edited
by admin
on Mon Mar 31 21:32:03 GMT 2025
Record UNII
4Y3VYY2X83
Record Status Validated (UNII)
Record Version
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Name Type Language
BIX-02188
Common Name English
BIX02188
Preferred Name English
(Z)-3-(((3-((DIMETHYLAMINO)METHYL)PHENYL)AMINO)(PHENYL)METHYLENE)-2-OXOINDOLINE-6-CARBOXAMIDE
Systematic Name English
1H-INDOLE-6-CARBOXAMIDE, 3-(((3-((DIMETHYLAMINO)METHYL)PHENYL)AMINO)PHENYLMETHYLENE)-2,3-DIHYDRO-2-OXO-, (3Z)-
Systematic Name English
Code System Code Type Description
PUBCHEM
66524294
Created by admin on Mon Mar 31 21:32:03 GMT 2025 , Edited by admin on Mon Mar 31 21:32:03 GMT 2025
PRIMARY
CAS
1094614-84-2
Created by admin on Mon Mar 31 21:32:03 GMT 2025 , Edited by admin on Mon Mar 31 21:32:03 GMT 2025
PRIMARY
FDA UNII
4Y3VYY2X83
Created by admin on Mon Mar 31 21:32:03 GMT 2025 , Edited by admin on Mon Mar 31 21:32:03 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY