ChemicalBook > CAS DataBase List > IPA-3

IPA-3

Product Name
IPA-3
CAS No.
42521-82-4
Chemical Name
IPA-3
Synonyms
IPA 3;IPA 3;IPA3;1'-Dithiodi-2-naphthtol;1,1'-Dithiodi-2-naphthtol;2-Naphthalenol, 1,1'-dithiobis-;Bis(2-hydroxy-1-naphthyl) disulfide;1,1′-Disulfanediyldinaphthalen-2-ol;1,1'-Dithiodi-2-naphthtol USP/EP/BP;1,1'-Disulfanediylbis(naphthalen-2-ol);1,1'-Disulfanediylbis(naphthalen-2-ol)
CBNumber
CB02518903
Molecular Formula
C20H14O2S2
Formula Weight
350.45
MOL File
42521-82-4.mol
More
Less

IPA-3 Property

Melting point:
172℃
Boiling point:
543.7±35.0 °C(Predicted)
Density 
1.46±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO: >20mg/mL
pka
7.52±0.50(Predicted)
form 
Yellow solid
color 
off-white to yellow
Water Solubility 
Soluble in DMSO or ethanol. Insoluble in water.
Sensitive 
Light Sensitive
Stability:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
CAS DataBase Reference
42521-82-4
More
Less

Safety

Hazard Codes 
Xi,N
Risk Statements 
41-50/53
Safety Statements 
26-39-60-61
RIDADR 
UN 3077 9 / PGIII
WGK Germany 
3
HazardClass 
9
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H318Causes serious eye damage

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
506106
Product name
p21-Activated Kinase Inhibitor III, IPA-3
Packaging
5mg
Price
$144
Updated
2024/03/01
Sigma-Aldrich
Product number
506106
Product name
p21-Activated Kinase Inhibitor III, IPA-3
Packaging
25mg
Price
$490
Updated
2024/03/01
Alfa Aesar
Product number
J65848
Product name
p21-Activated Kinase Inhibitor III, IPA-3
Packaging
5mg
Price
$122
Updated
2023/06/20
Alfa Aesar
Product number
J65848
Product name
p21-Activated Kinase Inhibitor III, IPA-3
Packaging
10mg
Price
$205
Updated
2023/06/20
Cayman Chemical
Product number
14759
Product name
IPA-3
Purity
≥95%
Packaging
5mg
Price
$57
Updated
2024/03/01
More
Less

IPA-3 Chemical Properties,Usage,Production

Description

IPA-3 (42521-82-4) is a selective allosteric inhibitor of Group 1 p21-activated kinase (PAK1 IC50?= 2.5 μM)1?via covalent binding to the PAK1 regulatory domain preventing binding to the upstream activator Cdc422. IPA-3 has been shown to induce cell death in human leukemic cell lines3, significantly inhibit TGFβ1-induced prostate cell epithelial to mesenchymal transition4?and inhibit the growth of liver cancer cells5.

Uses

p21-activated kinase 1 (PAK1) is a member of a family non-receptor serine/threonine kinases that are vital to normal cell function. Binding of various upstream partners to PAK1 results in release of an autoinhibitory domain that blocks activity of the kinase domain. PAK1 expression and activity is upregulated in several human cancers and is a potential therapeutic target for cancer intervention. IPA-3 is a cell-permeable allosteric inhibitor of PAK1 that is non-competitive with respect to ATP binding (IC50 = 2.5 μM). It does not, however, inhibit the activity of PAK1 that has been pre-activated with Cdc42. IPA-3 binds covalently to the PAK1 regulatory domain (apparent Kd = 1.9 uM) and prevents binding to the upstream activator Cdc42.[Cayman Chemical]

Uses

Acts as an allosteric inhibitor of Pak1

Definition

ChEBI: An organic disulfide obtained by oxidative dimerisation of 1-sulfanylnaphthalen-2-ol.

Biological Activity

IPA-3 is a selective non-ATP competitive Pak1 inhibitor with IC50 of 2.5 μM in a cell-free assay, no inhibition to group II PAKs (PAKs 4-6).

Biochem/physiol Actions

IPA-3 is an allosteric inhibitor of Pak1. It binds to autoinhibitory domain of Pak1 (p21 activated kinase), highly selective amongst kinases. Pak1 is implicated in tumorigenesis and metastasis.

in vitro

IPA-3 is a non ATP-competitive, allosteric inhibitor of p21-activated kinase 1 (Pak1). PIR3.5 is the control compound of IPA-3. IPA-3 prevents Cdc42-stimulated Pak1 autophosphorylation on Thr423. IPA-3 also prevents sphingosine-dependent Pak1 autophosphorylation. IPA-3 does not target exposed cysteine residues on Pak1. The disulfide bond of IPA-3 is critical for inhibition of Pak1 and in vitro reduction by the reducing agent dithiothreitol (DTT) abolishes Pak1 inhibition by IPA-3. IPA-3 inhibits activation of Pak1 by diverse activators, but does not inhibit preactivated Pak1. IPA-3 inhibits PDGF-stimulated Pak activation in mouse embryonic fibroblasts. IPA-3 inhibits Pak1 activation in part by binding covalently to the regulatory domain of Pak1. IPA-3 binds Pak1 covalently in a time- and temperature-dependent manner. IPA-3 prevents binding of the Pak1 activator Cdc42. IPA-3 binds directly to the Pak1 autoregulatory domain. IPA-3 reversibly inhibits PMA-induced membrane ruffling in cells.

storage

Store at -20°C

References

1) Deacon?et al.?(2008)?An isoform-selective, small-molecule inhibitor targets the autoregulatory mechanism of p21-activated kinase; Chem.Biol.,?14?322 2) Viaud and Peterson (2009)?An allosteric kinase inhibitor binds the p21-activated kinase (PAK) autoregulatory domain covalently; Mol. Cancer Ther.,?8?2559 3) Kuzelova?et al. (2014)?Group 1 PAK Inhibitor IPA-3 Induces Cell Death and Affects Cell Adhesivity to Fibronectin in Human Hematopoietic Cells; PLoS One,?9?e92560 4) Al-Azayzih?et al.?(2015)?P21 Activated Kinase-1 Mediates Transforming Growth factor b1-Induced Prostate Cancer Cell Epithelial to Mesenchymal transition; Biochim. Biophys. Acta,?1853?1229 5) Wong?et al.?(2013)?IPA-3 Inhibits the Growth of Liver Cancer Cells By Suppressing PAK1 and NF-kB Activation; PLoS One,?8?e68843

IPA-3 Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

IPA-3 Suppliers

VDM Biochemicals
Tel
0330-2528181
Fax
0330-2528171
Email
sales@vdmbio.com
Country
United States
ProdList
510
Advantage
64
MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9923
Advantage
65
Target molecule Corp.
Tel
857-239-0968
Fax
857-239-8801
Email
service1@targetmol.com
Country
United States
ProdList
2559
Advantage
60
Musechem
Tel
+1-800-259-7612
Fax
+1-800-259-7612
Email
info@musechem.com
Country
United States
ProdList
4660
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6391
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
TargetMol Chemicals Inc.
Tel
Email
support@targetmol.com
Country
United States
ProdList
38632
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
Focus Biomolecules
Tel
--
Fax
--
Email
sales@focusbiomolecules.com
Country
United States
ProdList
1284
Advantage
58
Sarchem Laboratories, Inc.
Tel
--
Fax
--
Email
info@sarchemlabs.com
Country
United States
ProdList
736
Advantage
58
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
Creative Enzymes
Tel
--
Fax
--
Email
info@creative-enzymes.com
Country
United States
ProdList
6057
Advantage
58
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Sarchem Laboratories, Inc.
Tel
--
Fax
--
Email
sarchem@aol.com
Country
United States
ProdList
198
Advantage
50
Santa Cruz Biotechnology, Inc.
Tel
--
Fax
--
Email
scbt@scbt.com
Country
United States
ProdList
3597
Advantage
60
Selleck Chemicals LLC
Tel
--
Fax
--
Email
info@selleckchem.com
Country
United States
ProdList
824
Advantage
60

42521-82-4, IPA-3Related Search:


  • 1,1'-Dithiodi-2-naphthtol
  • IPA 3
  • p21-Activated Kinase Inhibitor III, IPA-3
  • Bis(2-hydroxy-1-naphthyl) disulfide
  • 2-Naphthalenol, 1,1'-dithiobis-
  • 1,1′-Disulfanediyldinaphthalen-2-ol
  • IPA 3;IPA3
  • p21-Activated Kinase Inhibitor III, IPA-3 - CAS 42521-82-4 - Calbiochem
  • 1,1'-Disulfanediylbis(naphthalen-2-ol)
  • 1-[(2-hydroxy-1-naphthyl)disulfanyl]naphthalen-2-ol
  • 1'-Dithiodi-2-naphthtol
  • 1,1'-Dithiodi-2-naphthtol USP/EP/BP
  • inhibit,Inhibitor,IPA-3,p21 activated kinases,PAK
  • 1,1'-Disulfanediylbis(naphthalen-2-ol)
  • 42521-82-4
  • Inhibitors
  • PAK Inhibitor III, IPA-3
  • PAK Inhibitor III
  • 1,1'-disulfanediylbis(naphthalen-2-ol)