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J22352

CAS No.
2252395-44-9
Chemical Name:
J22352
Synonyms
J22352;J-22352,J22352;Benzamide, 4-[[3,4-dihydro-2,4-dioxo-3-(2-phenylethyl)-1(2H)-quinazolinyl]methyl]-N-hydroxy-
CBNumber:
CB55821267
Molecular Formula:
C24H21N3O4
Molecular Weight:
415.44
MDL Number:
MFCD32062835
MOL File:
2252395-44-9.mol
Last updated:2023-07-14 17:35:11

J22352 Properties

Density 1.343±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO:125.0(Max Conc. mg/mL);300.88(Max Conc. mM)
pka 8.91±0.10(Predicted)

J22352 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0090795 J22352 99.73% 2252395-44-9 5mg $120 2021-12-16 Buy
ChemScene CS-0090795 J22352 99.73% 2252395-44-9 10mg $190 2021-12-16 Buy
ChemScene CS-0090795 J22352 99.73% 2252395-44-9 50mg $550 2021-12-16 Buy
ChemScene CS-0090795 J22352 99.73% 2252395-44-9 100mg $940 2021-12-16 Buy
Product number Packaging Price Buy
CS-0090795 5mg $120 Buy
CS-0090795 10mg $190 Buy
CS-0090795 50mg $550 Buy
CS-0090795 100mg $940 Buy

J22352 Chemical Properties,Uses,Production

Description

J22352 is a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor. J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma cancers, and leading to the restoration of host antitumor activity by reducing the immunosuppressive activity of PD-L1.

in vitro

The consequences of decreased HDAC6 expression in response to J22352 decreased cell migration, increased autophagic cancer cell death and significant tumor growth inhibition. Notably, J22352 reduced the immunosuppressive activity of PD-L1, leading to the restoration of host anti-tumor activity. These results demonstrate that J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma._x000D_ _x000D_ Reference: Biochem Pharmacol. 2019 May;163:458-471. https://pubmed.ncbi.nlm.nih.gov/30885763/

in vivo

The consequences of decreased HDAC6 expression in response to J22352 decreased cell migration, increased autophagic cancer cell death and significant tumor growth inhibition. Notably, J22352 reduced the immunosuppressive activity of PD-L1, leading to the restoration of host anti-tumor activity. These results demonstrate that J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma._x000D_ _x000D_ Reference: Biochem Pharmacol. 2019 May;163:458-471. https://pubmed.ncbi.nlm.nih.gov/30885763/

target

J22352 is a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC50 value of 4.7 nM.

J22352 Preparation Products And Raw materials

Raw materials

Preparation Products

J22352 Suppliers

Global( 9)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Aladdin Scientific
+1-+1(833)-552-7181 sales@aladdinsci.com United States 52927 58
Fan De(Beijing) Biotechnology Co., Ltd. 15911056312 liming@bio-fount.com China 9730 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
Shanghai hongqu biomedical technology co. LTD 88888888888 hongquchem@qq.com China 5132 58
cjbscvictory 13348960310 13348960310 3003867561@qq.com China 10011 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24017 58
RD International Technology Co., Limited 18024082417 market@ubiochem.com China 9180 58
J22352 Benzamide, 4-[[3,4-dihydro-2,4-dioxo-3-(2-phenylethyl)-1(2H)-quinazolinyl]methyl]-N-hydroxy- J-22352,J22352 2252395-44-9