Ferroptosis-centered Drug Response Information
General Information of the Drug (ID: ferrodrug0228)
Name |
Ginkgolide B
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Synonyms |
Ginkgolide B; 15291-77-7; Ginkolide B; Gingko lactone; BN 52021; SR-01000597598; bn52021; Ginklide B; 7-Deoxyginkgolide C; CHEMBL266625; SCHEMBL14279903; 1-Hydroxy-(1beta)-Ginkgolide A; BCP25992; NSC110257; PDSP1_000734; PDSP2_000724; AKOS015895882; NSC-110257; tert-butyl-trihydroxy-methyl-[?]trione; NCGC00025245-01; 99796-69-7; AS-56165; L000993; SR-01000597598-1; SR-01000597598-3; 8-tert-butyl-6,12,17-trihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.01,11.03,7.07,11.013,17]nonadecane-5,15,18-trione
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Status |
Terminated
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Drug Type |
Small molecular drug
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Structure |
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3D MOL
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Formula |
C20H24O10
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IUPAC Name |
8-tert-butyl-6,12,17-trihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.01,11.03,7.07,11.013,17]nonadecane-5,15,18-trione
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Canonical SMILES |
CC1C(=O)OC2C1(C34C(=O)OC5C3(C2O)C6(C(C5)C(C)(C)C)C(C(=O)OC6O4)O)O
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InChI |
InChI=1S/C20H24O10/c1-6-12(23)28-11-9(21)18-8-5-7(16(2,3)4)17(18)10(22)13(24)29-15(17)30-20(18,14(25)27-8)19(6,11)26/h6-11,15,21-22,26H,5H2,1-4H3
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InChIKey |
SQOJOAFXDQDRGF-UHFFFAOYSA-N
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PubChem CID | |||||
TTD Drug ID |
Full List of Ferroptosis Target Related to This Drug
Nuclear factor erythroid 2-related factor 2 (NFE2L2)
In total 1 item(s) under this Target | |||||
Experiment 1 Reporting the Ferroptosis-centered Drug Act on This Target | [1] | ||||
Target for Ferroptosis | Marker/Suppressor | ||||
Responsed Disease | Nonalcoholic fatty liver disease | ICD-11: DB92 | |||
Pathway Response | Fatty acid metabolism | hsa01212 | |||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
In Vitro Model | Hep-G2 cells | Hepatoblastoma | Homo sapiens | CVCL_0027 | |
In Vivo Model |
Male 8-week-old C57/BL6 ApoE-/-mice of weight (22~25 g) were purchased from Changzhou Cavens experimental animal Co., Ltd (Jiangsu, China). After 5 weeks of feeding, HFD-fed mice were randomly assigned into 4 groups (n = 10) : HFD group (0.9 % sodium chloride by gavage), GB-L group (at a high dose of 20 mg kg-1d-1 GB in 0.9 % sodium chloride by gavage), GB-H group (at a high dose of 30 mg kg-1d-1 GB in 0.9 % sodium chloride by gavage), and Ato group (1.3 mg kg-1d-1 Ato in 0.9 % sodium chloride by gavage) as a positive control. The mice in ND group were given the same volume of 0.9 % sodium chloride.
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Response regulation | Ginkgolide B (GB), a main constituent of Ginkgo biloba extracts, reduces hepatic lipid accumulation and ameliorates nonalcoholic fatty liver disease (NAFLD) in obese mice. Remarkably, after Nrf2 interference, GB treatment significantly increased Nrf2 expression, indicating that GB exerted anti-ferroptosis effects by activation of Nrf2 pathway. | ||||