ARD-2128

ARD-2128 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354
Email: support@targetmol.com
Products Intro: Product Name:ARD-2128
CAS:2222111-87-5
Package:1 mg;1 mL * 10mM (in DMSO);10 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Aladdin Scientific
Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:ARD-2128
CAS:2222111-87-5
Purity:99% Package:$280.9/1mg;$700.9/5mg;$1150.9/10mg;Bulk package Remarks:99%
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185
Email: sales-cpd@caerulumpharma.com
Products Intro: Product Name:ARD-2128
CAS:2222111-87-5
Package:10g;1g;100mg;10mg
Company Name: DC Chemicals  
Tel: 021-58447131 13564518121
Email: sales@dcchemicals.com
Products Intro: Product Name:ARD-2128
CAS:2222111-87-5
Purity:98% HPLC Package:100mg,250mg,1g
Company Name: Chunchuang (Wuhan) Technology Co., Ltd  
Tel: 15342225168
Email: yutianchun2007@126.com
Products Intro: Product Name:1mg;1g;10g;100g;1Kg;
CAS:2222111-87-5
Purity:99.5+HPLC
ARD-2128 Basic information
Product Name:ARD-2128
Synonyms:ARD-2128;orally,ARD2128,AR-regulated,bioavailable,inhibit,ARD 2128,Inhibitor,prostate,Androgen Receptor,cancer,ARD-2128,tumor,PROTACs;Benzamide, N-[trans-3-(3-chloro-4-cyanophenoxy)-2,2,4,4-tetramethylcyclobutyl]-4-[4-[[1-[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-5-yl]-4-piperidinyl]methyl]-1-piperazinyl]-
CAS:2222111-87-5
MF:C45H50ClN7O6
MW:820.37
EINECS:
Product Categories:
Mol File:2222111-87-5.mol
ARD-2128 Structure
ARD-2128 Chemical Properties
Boiling point 1000.4±65.0 °C(Predicted)
density 1.39±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
form Solid
pka10.83±0.40(Predicted)
color Light yellow to green yellow
Safety Information
MSDS Information
ARD-2128 Usage And Synthesis
Biological ActivityARD-2128 is a highly potent, orally bioavailable PROTAC androgen receptor (AR) degrader. ARD-2128 effectively reduces AR protein, suppresses AR-regulated genes in tumor tissues, and inhibits growth of tumor without signs of toxicity. ARD-2128 has the potential for the research of the prostate cancer[1]. ARD-2128 is highly potent and effective in the inhibition of cell growth in the VCaP cell line and LNCaP cell line with the IC50 values of 4 nM and 5 nM, respectively[1].ARD-2128 (1, 10, 100, and 1000 nM; 24 hours) effectively reduces the AR protein level by >50% at 1 nM and achieves the AR degradation of >90% at 10, 100, and 1000 nM, respectively, in VCaP cell[1]. ARD-2128 (20 mg/kg; p.o.; once) is effective in reducing the level of AR protein in mice after 24 hours[1].ARD-2128 (10-40 mg/kg; p.o.; daily for 21 days) shows antitumor activity in the VCaP xenograft model in mice[1].ARD-2128 (5mg/kg; p.o.) treatment shows the Cmax, AUC0-t and t1/2 values of 1304 ng/mL, 22361 ng h/mL and 18.8 hours, respectively[1].
References[1]. Han X, et al. Strategies toward Discovery of Potent and Orally Bioavailable Proteolysis Targeting Chimera Degraders of Androgen Receptor for the Treatment of Prostate Cancer [published online ahead of print, 2021 Aug 25]. J Med Chem. 2021;10.1021/acs.jmedchem.1c00882.
ARD-2128 Preparation Products And Raw materials
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