Page last updated: 2024-10-15

liproxstatin-1

Description

liproxstatin-1: suppress ferroptosis in cells [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

liproxstatin-1 : An azaspiro compound that is 1'H-spiro[piperidine-4,2'-quinoxaline] in which the hydrogen at position 3' is replaced by a (3-chlorobenzyl)amino group. It is a potent inhibitor of ferroptosis. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID135735917
CHEMBL ID2094750
CHEBI ID173097
SCHEMBL ID17757281
MeSH IDM000603227

Synonyms (27)

Synonym
liproxstatin 1
lip-1
n-(3-chlorobenzyl)-1'h-spiro[piperidine-4,2'-quinoxalin]-3'-amine
CHEBI:173097
n-[(3-chlorophenyl)methyl]-1'h-spiro[piperidine-4,2'-quinoxalin]-3'-amine
liproxstatin1
liproxstatin-1
950455-15-9
CCG-175950
AKOS001973583
CHEMBL2094750
dndi1417503
S7699
CS-3994
AC-33023
HY-12726
EX-A558
n-[(3-chlorophenyl)methyl]-1'h-spiro[piperidine-4,2'-quinoxaline]-3'-amine
SCHEMBL17757281
liproxstatin-1, >98% (hplc)
BCP15985
F17363
mfcd14948691
BS-18273
n-[(3-chlorophenyl)methyl]spiro[4h-quinoxaline-3,4'-piperidine]-2-amine
n-[(3-chlorophenyl)methyl]spiro[1,4-dihydroquinoxaline-3,4'-piperidine]-2-imine
EN300-202271
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
ferroptosis inhibitorAny substance that inhibits the process of ferroptosis (a type of programmed cell death dependent on iron and characterized by the accumulation of lipid peroxides) in organisms.
radical scavengerA role played by a substance that can react readily with, and thereby eliminate, radicals.
antioxidantA substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
cardioprotective agentAny protective agent that is able to prevent damage to the heart.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (4)

ClassDescription
monochlorobenzenesAny member of the class of chlorobenzenes containing a mono- or poly-substituted benzene ring in which only one substituent is chlorine.
secondary amino compoundA compound formally derived from ammonia by replacing two hydrogen atoms by organyl groups.
azaspiro compoundAn azaspiro compound is a spiro compound in which at least one of the cyclic components is a nitrogen heterocyle.
organic heterotricyclic compoundAn organic tricyclic compound in which at least one of the rings of the tricyclic skeleton contains one or more heteroatoms.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1725773Inhibition of erastin-induced cell death in FRDA patient-derived fibroblast assessed as depletion of cellular ATP incubated for 12 hrs followed by erastin stimulation and measured after by luciferase-linked ATPase enzymatic assay2020ACS medicinal chemistry letters, Nov-12, Volume: 11, Issue:11
Antiferroptotic Activity of Phenothiazine Analogues: A Novel Therapeutic Strategy for Oxidative Stress Related Disease.
AID1725772Anti-ferroptotic activity in FRDA patient-derived Lymphocyte assessed as reduction in RSL3-induced lipid peroxidation incubated for overnight followed by RSL3 stimulation and measured after 90 mins by FACS analysis2020ACS medicinal chemistry letters, Nov-12, Volume: 11, Issue:11
Antiferroptotic Activity of Phenothiazine Analogues: A Novel Therapeutic Strategy for Oxidative Stress Related Disease.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (36)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's12 (33.33)24.3611
2020's24 (66.67)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews7 (19.44%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other29 (80.56%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]