Ferroptosis-centered Drug Response Information
General Information of the Drug (ID: ferrodrug0152)
Name |
Methyl vinyl ketone
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Synonyms |
METHYL VINYL KETONE; 3-Buten-2-one; but-3-en-2-one; 78-94-4; Butenone; Vinyl methyl ketone; Methylene acetone; 2-Butenone; Methylvinylketon; Acetyl ethylene; 1-Buten-3-one; 3-Butene-2-one; Methyl ethenyl ketone; Methylvinyl ketone; Methylvinylketone; 3-Butenone-2; Acetone, methylene-; Ketone, methyl vinyl; gamma-Oxo-alpha-butylene; Methyl-vinyl-cetone; 3-oxo-1-butene; but-1-en-3-one; methylvinylcetone; 3-Oxobutene; NSC 4853; UN1251; CHEBI:48058; Delta(3)-2-butenone; CH2=CHCOCH3; 25038-87-3; AR7642I1MP; CHEMBL1600824; DTXSID3025671; NSC-4853; Methgl vinyl ketone; Methylvinylketon [German]; delta(sup 3)-2-Butenone; Methyl-vinyl-cetone [French]; CCRIS 3423; HSDB 716; EINECS 201-160-6; UNII-AR7642I1MP; AI3-16048; 3-butenone; methyl vinylketone; methyl-vinylketone; methylvinyl-ketone; but-3-enone; buten-2-one; g-oxo-a-Butylene; metyl vinyl ketone; 3-oxo-l-butene; methly vinyl ketone; methyl-vinyl-ketone; 1-butene-3-one; 3-Butenen-2-one; 1-Propen-3-one; MFCD00008777; 3-oxo-but-1-ene; EC 201-160-6; .DELTA.3-2-BUTENONE; .gamma.-Oxo-.alpha.-butylene; DTXCID205671; Methyl vinyl ketone, stabilized; WLN: 1V1U1; METHYL VINYL KETONE [MI]; NSC4853; BCP24759; Tox21_200363; BDBM50245462; LMFA12000018; STL299803; .DELTA.-OXO-.ALPHA.-BUTYLENE; AKOS000120352; UN 1251; UN-1251; CAS-78-94-4; NCGC00091118-01; NCGC00091118-02; NCGC00257917-01; M0460; 3-Buten-2-one, purum, >=95.0% (GC); EN300-19794; C20701; F71092; M-6580; Q417525; InChI=1/C4H6O/c1-3-4(2)5/h3H,1H2,2H; Methyl vinyl ketone, stabilized [UN1251] [Poison]; 3-Buten-2-one, contains 0.3-1.0% hydroquinone as stabilizer, technical grade, 90%; 3-Buten-2-one, contains 0.5% hydroquinone and 0.1% acetic acid as stabilizer, 99%
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Status |
Investigative
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Drug Type |
Small molecular drug
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Structure |
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Formula |
C4H6O
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IUPAC Name |
but-3-en-2-one
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Canonical SMILES |
CC(=O)C=C
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InChI |
InChI=1S/C4H6O/c1-3-4(2)5/h3H,1H2,2H3
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InChIKey |
FUSUHKVFWTUUBE-UHFFFAOYSA-N
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PubChem CID |
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 | Aortic aneurysm | ICD-11: BD50 | |||
Pathway Response | Fatty acid metabolism | hsa01212 | |||
Ferroptosis | hsa04216 | ||||
Cell Process | Cell ferroptosis | ||||
In Vitro Model | rVSMCs (Rat vascular smooth muscle cells) | ||||
A7r5 cells | Normal | Rattus norvegicus | CVCL_0137 | ||
EAhy926 cells | Normal | Homo sapiens | CVCL_3901 | ||
C3H/10T1/2 cells | Normal | Mus musculus | CVCL_0190 | ||
In Vivo Model |
C57BL/6J wild-type mice (8-10 wk old, male) were purchased from Japan SLC (Tokyo, Japan). Mice were housed (4/cage, RAIR HD-ventilated micro-isolator animal housing systems; Laboratory Products, Seaford, DE) in an environment maintained at 23 ± 2 with ad libitum access to food and water under a 12-h:12-h light-dark cycle, with lights on from 0800 to 2000. A total of 13 mice were used. The aorta was harvested immediately after mice were euthanized by inhalation of carbon dioxide, washed in 0.1% antibiotics/PBS, and cut into 3-4-mm rings. The aortic rings were cultured in 10% FCS/DMEM for 3 h and then treated with CSE (0.8 mg/mL) for the indicated periods.
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Response regulation | VSMC ferroptosis was induced by acrolein and methyl vinyl ketone, major constituents of CSE. CSE also induced the upregulation of Ptgs2 mRNA, lipid peroxidation, and intracellular GSH depletion, which are key features of ferroptosis. These findings suggest that ferroptosis is a potential therapeutic target for preventing aortic aneurysm and dissection. | ||||