Page last updated: 2024-09-26

s 23121

Description

S 23121: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

flumipropyn : A racemate comprising equimolar amounts of (R)- and (S)-flumipropynflumipropyn. A protoporphyrinogen oxidase inhibitor introduced by the Sumitomo Chemical Co., it was formerly used for the control of grasses and broad-leaved weeds in various crops. [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]

2-[5-(but-3-yn-2-yloxy)-4-chloro-2-fluorophenyl]-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione : A dicarboximide that is 4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione in which the nitrogen has been substituted by a 5-(but-3-yn-2-yloxy)-4-chloro-2-fluorophenyl group. [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 CID158434
CHEMBL ID2287110
CHEBI ID139040
CHEBI ID5105
SCHEMBL ID38980
MeSH IDM0222027

Synonyms (24)

Synonym
flumipropyn
84478-52-4
C10993 ,
s-23121
CHEBI:139040
2-[5-(but-3-yn-2-yloxy)-4-chloro-2-fluorophenyl]-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dione
2-(5-but-3-yn-2-yloxy-4-chloro-2-fluorophenyl)-4,5,6,7-tetrahydroisoindole-1,3-dione
AC1L4JX1 ,
y3e93z8tul ,
s 23121
1h-isoindole-1,3(2h)-dione, 2-(4-chloro-2-fluoro-5-((1-methyl-2-propynyl)oxy)phenyl)-4,5,6,7-tetrahydro-
n-(4-chloro-2-fluoro-5-((1-methyl-2-propynyl)oxy)phenyl)-3,4,5,6-tetrahydrophthalimide
flumipropyn [iso:bsi]
unii-y3e93z8tul
chebi:5105
CHEMBL2287110
SCHEMBL38980
DTXSID90868818
2-{5-[(but-3-yn-2-yl)oxy]-4-chloro-2-fluorophenyl}-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dione
Q27106661
flumipropyn [iso]
2-(4-chloro-2-fluoro-5-((1-methyl-2-propyn-1-yl)oxy)phenyl)-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dione
1h-isoindole-1,3(2h)-dione, 2-(4-chloro-2-fluoro-5-((1-methyl-2-propyn-1-yl)oxy)phenyl)-4,5,6,7-tetrahydro-
2-(5-but-3-yn-2-yloxy-4-chloro-2-fluoro-phenyl)-4,5,6,7-tetrahydroisoindole-1,3-dione

Drug Classes (6)

ClassDescription
dicarboximideAn imide in which the two acyl substituents on nitrogen are carboacyl groups.
terminal acetylenic compoundAn acetylenic compound which a carbon of the C#C moiety is attached to a hydrogen atom.
aromatic etherAny ether in which the oxygen is attached to at least one aryl substituent.
monofluorobenzenesAny member of the class of fluorobenzenes containing a mono- or poly-substituted benzene ring carrying a single fluorine substitutent.
monochlorobenzenesAny member of the class of chlorobenzenes containing a mono- or poly-substituted benzene ring in which only one substituent is chlorine.
pyrrolineAny organic heteromonocyclic compound with a structure based on a dihydropyrrole.
[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]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's0 (0.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)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%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research Highlights

Safety/Toxicity (3)

ArticleYear
Close link between protoporphyrin IX accumulation and developmental toxicity induced by N-phenylimide herbicides in rats.
Birth defects research. Part B, Developmental and reproductive toxicology, Volume: 101, Issue: 6
2014
Dermal developmental toxicity of N-phenylimide herbicides in rats.
Birth defects research. Part B, Developmental and reproductive toxicology, Volume: 101, Issue: 2
2014
Difference in developmental toxicity among structurally similar N-phenylimide herbicides in rats and rabbits.
Birth defects research. Part B, Developmental and reproductive toxicology, Volume: 98, Issue: 6
2013
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Dosage (1)

ArticleYear
Metabolism of N-[4-chloro-2-fluoro-5-[(1-methyl-2- propynl)oxy]phenyl]-3,4,5,6-tetrahydrophthalimide (S-23121) in the rat: I. Identification of a new, sulphonic acid type of conjugate.
Xenobiotica; the fate of foreign compounds in biological systems, Volume: 23, Issue: 6
1993
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]