Ferroptosis-centered Drug Response Information
General Information of the Drug (ID: ferrodrug0204)
Name |
Oxaliplatin
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Synonyms |
oxaliplatin; DTXSID0036760; Oxalato(trans-l-1,2-cyclohexanediamine)platinum(II); cis-oxalato-trans-l-1,2-diaminocyclohexaneplatinum(II); DTXCID8016760; CAS-61825-94-3; NCGC00167798-01; SCHEMBL19511; HMS3269F19; Tox21_112585; Tox21_112629; AKOS005766023; AKOS015855804; CS-0992; BP-25383; HY-17371; [(1S,2S)-2-azanidylcyclohexyl]azanide; oxalate; platinum(4+)
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Structure |
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3D MOL
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Formula |
C8H14N2O4Pt
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IUPAC Name |
[(1R,2R)-2-azanidylcyclohexyl]azanide;oxalic acid;platinum(2+)
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Canonical SMILES |
C1CCC(C(C1)[NH-])[NH-].C(=O)(C(=O)O)O.[Pt+2]
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InChI |
InChI=1S/C6H12N2.C2H2O4.Pt/c7-5-3-1-2-4-6(5)8;3-1(4)2(5)6;/h5-8H,1-4H2;(H,3,4)(H,5,6);/q-2;;+2/t5-,6-;;/m1../s1
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InChIKey |
DRMCATBEKSVAPL-BNTLRKBRSA-N
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PubChem CID |
Full List of Ferroptosis Target Related to This Drug
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 | Hepatocellular carcinoma | ICD-11: 2C12 | ||
Responsed Regulator | LINC01134 (IncRNA) | Suppressor | ||
Pathway Response | Ferroptosis | hsa04216 | ||
Fatty acid metabolism | hsa01212 | |||
Apoptosis | hsa04210 | |||
Cell Process | Cell ferroptosis | |||
Cell apoptosis | ||||
In Vitro Model | Hep-G2 cells | Hepatoblastoma | Homo sapiens | CVCL_0027 |
Huh-7 cells | Hepatocellular carcinoma | Homo sapiens | CVCL_0336 | |
Response regulation | LINC01134 was positively correlated with GPX4 or Nrf2, demonstrating the clinical significance of LINC01134, Nrf2 and GPX4 in OXA resistance of hepatocellular carcinoma (HCC). Silenced LINC01134 enhances Oxaliplatin sensitivity by facilitating ferroptosis through GPX4 in hepatocarcinoma. | |||
Nuclear factor erythroid 2-related factor 2 (NFE2L2)
In total 2 item(s) under this Target | ||||
Experiment 1 Reporting the Ferroptosis-centered Drug Act on This Target | [1] | |||
Target for Ferroptosis | Marker/Suppressor | |||
Responsed Disease | Hepatocellular carcinoma | ICD-11: 2C12 | ||
Responsed Regulator | LINC01134 (IncRNA) | Suppressor | ||
Pathway Response | Ferroptosis | hsa04216 | ||
Fatty acid metabolism | hsa01212 | |||
Apoptosis | hsa04210 | |||
Cell Process | Cell ferroptosis | |||
Cell apoptosis | ||||
In Vitro Model | Hep-G2 cells | Hepatoblastoma | Homo sapiens | CVCL_0027 |
Huh-7 cells | Hepatocellular carcinoma | Homo sapiens | CVCL_0336 | |
Response regulation | LINC01134 was positively correlated with GPX4 or Nrf2, demonstrating the clinical significance of LINC01134, Nrf2 and GPX4 in OXA resistance of hepatocellular carcinoma. Silenced LINC01134 enhances Oxaliplatin sensitivity by facilitating ferroptosis through GPX4 in hepatocarcinoma. | |||
Experiment 2 Reporting the Ferroptosis-centered Drug Act on This Target | [2] | |||
Target for Ferroptosis | Marker/Suppressor | |||
Responsed Disease | Colorectal cancer | ICD-11: 2B91 | ||
Pathway Response | Fatty acid metabolism | hsa01212 | ||
Ferroptosis | hsa04216 | |||
Cell Process | Cell ferroptosis | |||
Cell proliferation | ||||
In Vitro Model | HT29 cells | Colon cancer | Mus musculus | CVCL_A8EZ |
Response regulation | Oxaliplatin promoted ferroptosis and oxidative stress in colorectal cancer cells by inhibiting the Nrf2 signaling pathway. Treatment with oxaliplatin enhanced the effects of erastin on CRC cells by promoting ferroptosis and oxidative stress and inhibiting cell viability. | |||
References