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

Details

Stereochemistry ACHIRAL
Molecular Formula C20H14O2S2
Molecular Weight 350.454
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IPA-3

SMILES

OC1=CC=C2C=CC=CC2=C1SSC3=C4C=CC=CC4=CC=C3O

InChI

InChIKey=RFAXLXKIAKIUDT-UHFFFAOYSA-N
InChI=1S/C20H14O2S2/c21-17-11-9-13-5-1-3-7-15(13)19(17)23-24-20-16-8-4-2-6-14(16)10-12-18(20)22/h1-12,21-22H

HIDE SMILES / InChI

Molecular Formula C20H14O2S2
Molecular Weight 350.454
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

IPA-3 (2,29- dihydroxy-1,19-dinaphthyldisuifide) is a highly selective, non-ATP-competitive allosteric inhibitor of PAK1 whose hyperactivity has been shown to be closely related with tumorigenesis. IPA-3 prevented Cdc42-induced PAK1 autophosphorylation on T423 and significantly inhibited PAK1 catalytic activity. The inhibitory action of IPA-3 is achieved in part by binding covalently to the regulatory domain of PAK1 which in turn prevented the physical interaction with Cdc42 or other GTPase activators. Increasing data implicates Pak1 in tumorigenesis and metastasis, thus suggesting that IPA-3 could be a novel oncologic therapy.

Originator

Curator's Comment: Deacon SW et al. at Fox Chase Cancer Center, USA

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
2.5 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
An allosteric kinase inhibitor binds the p21-activated kinase autoregulatory domain covalently.
2009-09
An isoform-selective, small-molecule inhibitor targets the autoregulatory mechanism of p21-activated kinase.
2008-04
Patents

Patents

Sample Use Guides

Mice: Control (DMSO), IPA-3 (2 mg/kg) and IPA-3 (4 mg/kg). IPA-3 was formulated in DMSO and administrated three times weekly (TIW) (2 mg/kg or 4 mg/kg) by intraperitoneal injection (i.p.) during the study and the tumor size was recorded twice a week.
Route of Administration: Intraperitoneal
10 uM IPA-3 prevented Cdc42-stimulated Pak1 autophosphorylation on Thr423. Dramatic inhibition of kinase activity in the presence 10 uM IPA-3 but not PIR-3.5 was observed for all three Group I Paks (Paks 1–3), with the strongest inhibition observed for Pak1. IPA-3 at 10 uM inhibited Pak1 activity by 95% ± 3%.
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:16:11 GMT 2025
Edited
by admin
on Mon Mar 31 22:16:11 GMT 2025
Record UNII
3XFG6MQ9G2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IPA-3
Common Name English
1,1'-DITHIODI-2-NAPHTHOL
Preferred Name English
2-NAPHTHALENOL, 1,1'-DITHIOBIS-
Systematic Name English
BIS(2-HYDROXY-1-NAPHTHYL) DISULFIDE
Systematic Name English
2-NAPHTHOL, 1,1'-DITHIODI-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID70195311
Created by admin on Mon Mar 31 22:16:11 GMT 2025 , Edited by admin on Mon Mar 31 22:16:11 GMT 2025
PRIMARY
CAS
42521-82-4
Created by admin on Mon Mar 31 22:16:11 GMT 2025 , Edited by admin on Mon Mar 31 22:16:11 GMT 2025
PRIMARY
CAS
1081767-20-5
Created by admin on Mon Mar 31 22:16:11 GMT 2025 , Edited by admin on Mon Mar 31 22:16:11 GMT 2025
SUPERSEDED
PUBCHEM
521106
Created by admin on Mon Mar 31 22:16:11 GMT 2025 , Edited by admin on Mon Mar 31 22:16:11 GMT 2025
PRIMARY
FDA UNII
3XFG6MQ9G2
Created by admin on Mon Mar 31 22:16:11 GMT 2025 , Edited by admin on Mon Mar 31 22:16:11 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY