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ARD-2128

CAS No.
2222111-87-5
Chemical Name:
ARD-2128
Synonyms
ARD-2128;orally,ARD2128,AR-regulated,bioavailable,inhibit,ARD 2128,Inhibitor,prostate,Androgen Receptor,cancer,ARD-2128,tumor,PROTACs;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]benzamide;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]-
CBNumber:
CB79731270
Molecular Formula:
C45H50ClN7O6
Molecular Weight:
820.37
MDL Number:
MFCD34567333
MOL File:
2222111-87-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:40

ARD-2128 Properties

Boiling point 1000.4±65.0 °C(Predicted)
Density 1.39±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Acetonitrile: Slightly Soluble: 1-10 mg/ml
form Solid
pka 10.83±0.40(Predicted)
color Light yellow to green yellow

ARD-2128 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 40964 ARD-2128 ≥98% 2222111-87-5 1mg $142 2026-04-30 Buy
Cayman Chemical 40964 ARD-2128 ≥98% 2222111-87-5 5mg $675 2026-04-30 Buy
Cayman Chemical 40964 ARD-2128 ≥98% 2222111-87-5 10mg $1065 2026-04-30 Buy
Cayman Chemical 40964 ARD-2128 ≥98% 2222111-87-5 25mg $2129 2026-04-30 Buy
ChemScene CS-0200331 ARD-2128 99.40% 2222111-87-5 1mg $303 2026-06-04 Buy
Product number Packaging Price Buy
40964 1mg $142 Buy
40964 5mg $675 Buy
40964 10mg $1065 Buy
40964 25mg $2129 Buy
CS-0200331 1mg $303 Buy

ARD-2128 Chemical Properties, Uses, Production

Uses

ARD-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].

Biological Activity

ARD-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].

in vivo

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].

Animal Model:SCID mice[1]
Dosage:20 mg/kg
Administration:Oral
Result:Reducing the level of AR protein in mice after 24 hours.
Animal Model:SCID mice[1]
Dosage:10, 20, and 40 mg/kg
Administration:P.o.; daily for 21 days
Result:Inhibits tumor growth by 46, 69, and 63%, respectively.
Animal Model:Male ICR Mice[1]
Dosage:5 mg/kg
Administration:P.o. (Pharmacokinetic Analysis)
Result:The Cmax, AUC0-t and t1/2 were 1304 ng/mL, 22361 ng h/mL and 18.8 hours, respectively.

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

Raw materials

Preparation Products

ARD-2128 Suppliers

Global Suppliers ( 24)
Supplier Tel Email Country ProdList Advantage
Nanjing Chemlin Chemical Co., Ltd 025-83697070 13770331960 info@chemlin.com.cn China 16305 64
ShangHai Caerulum Pharma Discovery Co., Ltd. 18149758185 18149758185 sales-cpd@caerulumpharma.com China 3493 58
Shanghai SuperLan Chemcial Technique Centre 0-2022843681 15618226720 chaolaichem@foxmail.com China 9996 58
BOC Sciences +1-631-485-4226 inquiry@bocsci.com United States 19935 58
Chunchuang (Wuhan) Technology Co., Ltd 15727060112 yutianchun2007@126.com China 9867 58
Beijing Jin Ming Biotechnology Co., Ltd. 010-60605840 psaitong@jm-bio.com China 27626 58
Changzhou Borl Biotechnology Co.,LTD 13656121842 luyan0021@163.com China 265 58
TargetMol Chemicals Inc. 4008200310 15002144251 marketing@tsbiochem.com China 24951 58
Nantong QuanYi Biotechnology Co., Ltd 0513-66337626 18051384581 sales@chemhifuture.com China 5985 58
Suzhou Haiben Pharmaceutical Co., Ltd 19353112242 1816280386@qq.com China 8041 58

ARD-2128 Spectrum

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]- 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]benzamide 2222111-87-5