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
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
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18420139
Curator's Comment: Deacon SW et al. at Fox Chase Cancer Center, USA
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL4600 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18420139 |
2.5 µM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23894351
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
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18420139
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%.
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 |
ACTIVE MOIETY