General Information of the Drug (ID: ferrodrug0373)
Name
XN4
Synonyms
(5S)-5-butyl-4-({1-[(4-chlorophenyl)methyl]-1H-imidazol-5-yl}methyl)-1-[3-(trifluoromethoxy)phenyl]piperazin-2-one; CHEMBL5171383; XN4

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Structure
Formula
C26H28ClF3N4O2
IUPAC Name
(5S)-5-butyl-4-[[3-[(4-chlorophenyl)methyl]imidazol-4-yl]methyl]-1-[3-(trifluoromethoxy)phenyl]piperazin-2-one
Canonical SMILES
CCCCC1CN(C(=O)CN1CC2=CN=CN2CC3=CC=C(C=C3)Cl)C4=CC(=CC=C4)OC(F)(F)F
InChI
InChI=1S/C26H28ClF3N4O2/c1-2-3-5-22-16-34(21-6-4-7-24(12-21)36-26(28,29)30)25(35)17-32(22)15-23-13-31-18-33(23)14-19-8-10-20(27)11-9-19/h4,6-13,18,22H,2-3,5,14-17H2,1H3/t22-/m0/s1
InChIKey
POBHWQSJZMJUAH-QFIPXVFZSA-N
PubChem CID
165416318
Full List of Ferroptosis Target Related to This Drug
Prostaglandin G/H synthase 2 (PTGS2)
In total 1 item(s) under this Target
Experiment 1 Reporting the Ferroptosis-centered Drug Act on This Target [1]
Target for Ferroptosis Marker
Responsed Disease Gastric cancer ICD-11: 2B72
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
In Vitro Model SGC-7901 cells Gastric carcinoma Homo sapiens CVCL_0520
BGC-823 cells Gastric carcinoma Homo sapiens CVCL_3360
GES-1 cells Normal Homo sapiens CVCL_EQ22
Response regulation The pro-ferroptotic role of XN4 in gastric cancer (GC) might enable it to become a promising drug for GC treatment in the future despite the need for extensive research. Moreover, GPX4 levels decreased, but NOX4 and ferroptosis-related protein PTGS2 levels increased in GC cells following XN4 treatment, which was nullified by NOX4 knockdown.
Phospholipid hydroperoxide glutathione peroxidase (GPX4)
In total 1 item(s) under this Target
Experiment 1 Reporting the Ferroptosis-centered Drug Act on This Target [1]
Target for Ferroptosis Suppressor
Responsed Disease Gastric cancer ICD-11: 2B72
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
In Vitro Model SGC-7901 cells Gastric carcinoma Homo sapiens CVCL_0520
BGC-823 cells Gastric carcinoma Homo sapiens CVCL_3360
GES-1 cells Normal Homo sapiens CVCL_EQ22
Response regulation The pro-ferroptotic role of XN4 in gastric cancer (GC) might enable it to become a promising drug for GC treatment in the future despite the need for extensive research. Moreover, GPX4 levels decreased, but NOX4 and ferroptosis-related protein PTGS2 levels increased in GC cells following XN4 treatment, which was nullified by NOX4 knockdown.
NADPH oxidase 4 (NOX4)
In total 1 item(s) under this Target
Experiment 1 Reporting the Ferroptosis-centered Drug Act on This Target [1]
Target for Ferroptosis Driver
Responsed Disease Gastric cancer ICD-11: 2B72
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
In Vitro Model SGC-7901 cells Gastric carcinoma Homo sapiens CVCL_0520
BGC-823 cells Gastric carcinoma Homo sapiens CVCL_3360
GES-1 cells Normal Homo sapiens CVCL_EQ22
Response regulation The pro-ferroptotic role of XN4 in gastric cancer (GC) might enable it to become a promising drug for GC treatment in the future despite the need for extensive research. Moreover, GPX4 levels decreased, but NOX4 and ferroptosis-related protein PTGS2 levels increased in GC cells following XN4 treatment, which was nullified by NOX4 knockdown.
References
Ref 1 A novobiocin derivative, XN4, triggers ferroptosis in gastric cancer cells via the activation of NOX4. Pharm Biol. 2022 Dec;60(1):1449-1457. doi: 10.1080/13880209.2022.2099431.