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IWR-1-endo

CAS No.
1127442-82-3
Chemical Name:
IWR-1-endo
Synonyms
IWR-1;CS-624;CS-1858;IWR-1-endo;endo-IWR 1;IWR-1-endo, >=98%;IWR-1(IWR-1-endo);IWR-1-endo USP/EP/BP;Wnt Antagonist I, IWR-1-endo;IWR-1-endo - IWR-1 | endo-IWR-1
CBNumber:
CB82518787
Molecular Formula:
C25H19N3O3
Molecular Weight:
409.44
MDL Number:
MFCD18086875
MOL File:
1127442-82-3.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

IWR-1-endo Properties

alpha -3.0~+3.0°(20℃/D)(c=0.1,CH3CN)
Boiling point 643.9±55.0 °C(Predicted)
Density 1.425±0.06 g/cm3(Predicted)
storage temp. room temp
solubility DMSO: soluble5mg/mL, clear
pka 11.88±0.43(Predicted)
form Liquid
color white to beige
Stability Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
WGK Germany  3

IWR-1-endo price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 681669 Wnt Antagonist I, IWR-1-endo Wnt Antagonist I, IWR-1-endo, is a cell-permeable inhibitor of TNKS1/PARP5a (IC?? = 131 nM) & TNKS2/PARP5b (IC??= 56 nM). Suppress Wnt-stimulated transcription activity (IC?? = 180 nM). 10MG $201 2024-03-01 Buy
Sigma-Aldrich 5.04462 InSolution Wnt Antagonist I, IWR-1-endo - CAS 1127442-82-3 - Calbiochem 1127442-82-3 5MG $118 2024-03-01 Buy
Sigma-Aldrich I0161 IWR-1 ≥98% (HPLC) 1127442-82-3 5mg $103 2023-06-20 Buy
Sigma-Aldrich I0161 IWR-1 ≥98% (HPLC) 1127442-82-3 25mg $393 2023-06-20 Buy
Cayman Chemical 13659 IWR-1-endo ≥98% 1127442-82-3 5mg $67 2024-03-01 Buy
Product number Packaging Price Buy
681669 10MG $201 Buy
5.04462 5MG $118 Buy
I0161 5mg $103 Buy
I0161 25mg $393 Buy
13659 5mg $67 Buy

IWR-1-endo Chemical Properties,Uses,Production

Description

IWR-1 endo (1127442-82-3) is a potent inhibitor of Wnt signaling (IC50=180 nM).1?Inhibits zebrafish tailfin regeneration (0.5 mM).2?Acts via inhibition of tankyrase and attenuates Wnt/β-catenin signaling in cancer stem-like cells.3?Promotes self-renewal and maintains pluripotency of human embryonic stem cells.4?Promotes differentiation of pluripotent stem cells into cardiomyocytes.5

Uses

IWR-3 act as inhibitors of Wnt response. It appear that IWR compounds induce stabilization of Axin proteins via a direct interaction, which is a part of the b-catenin destruction complex (consists of Apc, Axin, Ck1 and Gsk3b).Such compounds may be used in the treatment of Wnt protein signaling-related diseases and conditions such as cancer, degenerative diseases, type II diabetes and osteopetrosis.

Uses

IWR-1-endo act as inhibitors of Wnt response. It appear that IWR compounds induce stabilization of Axin proteins via a direct interaction, which is a part of the b-catenin destruction complex (consists of Apc, Axin, Ck1 and Gsk3b). Such compounds may be used in the treatment of Wnt protein signaling-related diseases and conditions such as cancer, degenerative diseases, type II diabetes and osteopetrosi s.

Definition

ChEBI: IWR-1-endo is a dicarboximide having an endo bridged phthalimide structure, substituted at nitrogen by a 4-(quinolin-8-ylcarbamoyl)benzoyl group. It has a role as an axin stabilizer and a Wnt signalling inhibitor. It is a dicarboximide, a bridged compound, a member of quinolines and a member of benzamides.

General Description

A cell-permeable p-imidobenzamidoquinoline, endo-diastereomer that is shown to inhibit the activity of TNKS1/PARP5a and TNKS2/PARP5b in in vitro auto-PARsylation assays (IC50 = 131 and 56 nM, respectively) and effectively suppress Wnt-stimulated transcription activity in L-Wnt-STF-based reporter assays (IC50 = 180 nM), while exhibiting little activity against PARP1 or PARP2 (IC50 >18.75 μM). Although both IWR-1-endo and XAV939 (Tankyrase1/2 Inhibitor; >Cat. No. 575545) act as reversible Wnt pathway inhibitors and exhibit similar pharmacological effects both in vitro and in vivo, IWR-1-endo exerts its effect via interaction with Axin, while XAV939 binds TNKS directly.

Biochem/physiol Actions

Cell permeable: yes

storage

Store at RT

References

1) Chen?et al. (2009),?Small molecule-mediated disruption of Wnt-dependent signaling in tissue regeneration and cancer; Nature Chem. Biol.,?5?100 2) Lu?et al.?(2009),?Structure-activity Relationship Studies of Small-Molecule Inhibitors of Wnt Response; Bioorg. Med. Chem. Lett.,?19?3825 3) Martins-Neves?et al.?(2018),?IWR-1, a tankyrase inhibitor, attenuates Wnt/?-catenin signaling in cancer stem-like cells and inhibits in vivo the growth of subcutaneous human osteosarcoma xenograft; Cancer Lett.,?414?1 4) Kim?et al.?(2013),?Modulations of ?-catenin function maintains mouse epiblast stem cell and human embryonic stem cell self-renewal; Nat. Commun., 4?4403 5) Ren?et al.?(2011),?Small Molecule Wnt Inhibitors Enhance the Efficiency of BMP-4-directed Cardiac Differentiation of Human Pluripotent Stem Cells; J. Mol. Cell. Cardiol.,?51?280

IWR-1-endo Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 134)Suppliers
Supplier Tel Email Country ProdList Advantage
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29220 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58

View Lastest Price from IWR-1-endo manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
IWR-1-endo pictures 2019-12-20 IWR-1-endo
1127442-82-3
US $1.00 / KG 1KG 99% 100kgs Career Henan Chemical Co
  • IWR-1-endo pictures
  • IWR-1-endo
    1127442-82-3
  • US $1.00 / KG
  • 99%
  • Career Henan Chemical Co

IWR-1-endo Spectrum

[(3aR*,4S*,7R*,7aS)-1,3,3a,4,7,7a-Hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl]-N-8-quinolinylbenzamide Benzamide, 4-[(3aR,4S,7R,7aS)-1,3,3a,4,7,7a-hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl]-N-8-quinolinyl-, rel- endo-IWR 1 IWR-1-endo rel-4-[(3aR,4S,7R,7aS)-1,3,3a,4,7,7a-Hexahydro-1,3-dioxo-4,7-Methano-2H-isoindol-2-yl]-N-8-quinolinylbenzaMide rel-4-[(3aR,4S,7R,7aS)-1,3,3a,4,7,7a-Hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl]-N-8-quinolinylbenzamide IWR-1-endo IWR-1-endo, >=98% ENDO-IWR 1;IWR-1-ENDO;IWR1;IWR 1 4-(1,3,3a,4,7,7a-Hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl)-N-8-quinolinyl-Benzamide (IWR-1) CS-1858 IWR-1(IWR-1-endo) IWR-1-endo - IWR-1 | endo-IWR-1 CS-624 Wnt Antagonist I, IWR-1-endo IWR-1-endo USP/EP/BP rel-4-((3aR,4S,7R,7aS)-1,3-Dioxo-1,3,3a,4,7,7a-hexahydro-2H-4,7-methanoisoindol-2-yl)-N-(quinolin-8-yl)benzamide IWR-1 1127442-82-3 Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Inhibitors