ChemicalBook >> CAS DataBase List >>4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)-

4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)-

CAS No.
1370032-20-4
Chemical Name:
4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)-
Synonyms
CUR5g;(E)-3-((1H-indol-3-yl)methylene)-5-((E)-4-hydroxybenzylidene)-1-methylpiperidin-4-one;4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)-
CBNumber:
CB812468517
Molecular Formula:
C22H20N2O2
Molecular Weight:
344.41
MDL Number:
MOL File:
1370032-20-4.mol
Last updated:2025-10-29 15:43:00

4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)- Properties

Boiling point 627.5±55.0 °C(Predicted)
Density 1.322±0.06 g/cm3(Predicted)
pka 9.38±0.30(Predicted)
form Solid
color Yellow to brown

4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)- Chemical Properties,Uses,Production

Uses

CUR5g is a potent autophagy inhibitor. CUR5g selectively inhibits autophagosome degradation in cancer cells by blocking autophagosome-lysosome fusion. CUR5g blocks the recruitment of STX17 to autophagosomes via a UVRAG-dependent mechanism, resulting in the inability of autophagosomes to fuse with lysosomes. CUR5g improves the anticancer effect of Cisplatin.html" class="link-product" target="_blank">Cisplatin (HY-17394) against A549 cells both in vitro and in vivo[1].

in vivo

CUR5g (40 mg/kg, Injected via caudal vein, once every 2 days for up to 15 days) exhibits synergistic anticancer effects with Cisplatin.html" class="link-product" target="_blank">Cisplatin (HY-17394) (1 mg/kg) and inhibits autophagic flux in vivo[1].

Animal Model:BALB/c nude mice (4-week-old, A549 cells were subcutaneously injected into the right scapula of each nude mouse)[1]
Dosage:40?mg/kg, CUR5g (40 mg/kg) and Cisplatin (1 mg/kg)
Administration:Injected via caudal vein, once every 2 days for up to 15 days
Result:Retarded the growth of xenografted tumors, whereas the combination treatment with Cisplatin almost completely inhibited tumor growth. Promoted the cisplatin sensitivity of A549 cells by inhibiting autophagic flux.

References

[1] Chen J, et al. CUR5g, a novel autophagy inhibitor, exhibits potent synergistic anticancer effects with cisplatin against non-small-cell lung cancer. Cell Death Discov. 2022 Oct 31;8(1):435. DOI:10.1038/s41420-022-01217-9

4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)- Preparation Products And Raw materials

Raw materials

Preparation Products

4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)- Suppliers

Global( 7)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai YuanYe Biotechnology Co., Ltd. 021-61312847; 18021002903 3008007409@qq.com China 71826 60
Tianjin Kailiqi Biotechnology Co., Ltd. 15076683720 klq@cw-bio.com China 8011 55
Changzhou Chenhong Biotechnology Co., Ltd. +86-0519-85788828 +86-13775037613 sales@chemrenpharm.com China 3934 58
Jinan Jiuli Biotechnology Co. , Ltd. 15865264761 486064515@qq.com China 4809 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11973 58
TargetMol Chemicals Inc. 15002134094 marketing@targetmol.cn China 29257 58
Guangzhou Weisheng Biotechnology Co., Ltd. 17765667235 CHINA 129 58

4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)- Spectrum

4-Piperidinone, 3-[(4-hydroxyphenyl)methylene]-5-(1H-indol-3-ylmethylene)-1-methyl-, (3E,5E)- CUR5g (E)-3-((1H-indol-3-yl)methylene)-5-((E)-4-hydroxybenzylidene)-1-methylpiperidin-4-one 1370032-20-4