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halopredone acetate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Halopredone acetate is a synthetic antipsychotic medication that belongs to the butyrophenone class. It is a potent dopamine receptor antagonist and is believed to exert its therapeutic effects by blocking the activity of dopamine in the brain. Halopredone acetate is a derivative of haloperidol, a well-established antipsychotic, but with increased potency. It was initially synthesized in the 1960s but has limited clinical use due to its high potency and potential for side effects. However, ongoing research continues to explore its potential applications in treating various psychiatric conditions, such as schizophrenia, bipolar disorder, and Tourette's syndrome. Researchers are interested in understanding its pharmacokinetic and pharmacodynamic properties to optimize its therapeutic potential and minimize adverse effects. Studies have demonstrated that halopredone acetate may have a faster onset of action compared to other antipsychotics. Further research is needed to fully characterize its clinical efficacy, safety profile, and optimal therapeutic applications. In summary, halopredone acetate is a potent antipsychotic with a complex pharmacological profile that continues to be investigated for its potential therapeutic uses.'

halopredone acetate: RN given refers to (6beta,11beta)-isomer; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID91667
CHEMBL ID2106520
CHEBI ID31665
SCHEMBL ID25316
MeSH IDM0065551

Synonyms (33)

Synonym
haloart
halopredone acetate
ths 201
einecs 260-951-4
halopredone diacetate
ccris 2685
17,21-bis(acetyloxy)-2-bromo-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione
2-bromo-6beta,9-difluoro-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dione 17,21-di(acetate)
pregna-1,4-diene-3,20-dione, 17,21-bis(acetyloxy)-2-bromo-6,9-difluoro-11-hydroxy-, (6beta,11beta)-
halopredone 17,21-diacetate
2-bromo-6beta,9-difluoro-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dione 17,21-diacetate
17,21-bis(acetyloxy)-2-bromo-6-beta,9-difluoro-11-beta-hydroxypregna-1,4-dien-3,20-dione
ths-201
halopredone acetate [usan:jan]
haloart (tn)
halopredone acetate (jan/usan)
D01743
57781-14-3
[2-[(6r,8s,9r,10s,11s,13s,14s,17r)-17-acetyloxy-2-bromo-6,9-difluoro-11-hydroxy-10,13-dimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate
24nul39jy1 ,
topicon
unii-24nul39jy1
CHEMBL2106520
halopredone acetate [mi]
halopredone acetate [usan]
pregna-1,4-diene-3,20-dione, 17,21-bis(acetyloxy)-2-bromo-6,9-difluoro-11-hydroxy-, (6.beta.,11.beta.)-
halopredone acetate [jan]
halopredone acetate [who-dd]
SCHEMBL25316
DTXSID30206477
CHEBI:31665
Q27253865
2-bromo-6beta,9-difluoro-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dione17,21-di(acetate)

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" In conclusion, systemic adverse effects were not observed in any dogs treated with THS-201."( A fifty-two-week chronic toxicity study of halopredone acetate (THS-201) in dogs.
Hayashi, T; Irimura, K; Morinaga, H; Morita, K; Yada, H; Yamashita, K, 1986
)
0.53
" The LD50 values of THS-201 both in mice and rats were estimated more than 5000 mg/kg at each route, and these are for above larger than those of TA or MPA."( [Study on toxicity of halopredone acetate. (I) Acute toxicity study in mice and rats].
Ichinohe, M; Kaga, M; Okazaki, S; Shinpo, K; Sudo, J; Takeuchi, M; Tanabe, T; Tsuga, T, 1985
)
0.58
"1 mg/kg, any toxic changes attributable to THS-201 were not observed."( [Study on toxicity of halopredone acetate. (II). Subacute toxicity study in rats].
Ichinohe, M; Kiguchi, M; Okazaki, S; Sato, M; Shimpo, K; Sudo, J; Takeuchi, M; Tanabe, T, 1985
)
0.58
"02 mg/kg, any toxic changes attributable to THS-201 were not observed."( [Study on toxicity of halopredone acetate. (III). Chronic toxicity study in rats].
Ichinohe, M; Ohta, Y; Okazaki, S; Shimpo, K; Sudo, J; Takeuchi, M; Tanabe, T, 1985
)
0.58
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
organic molecular entityAny molecular entity that contains carbon.
[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 (5)

Assay IDTitleYearJournalArticle
AID1133643Thymolytic activity in rat assessed as inhibition of thymus weight administered topically measured per pellet1977Journal of medicinal chemistry, Feb, Volume: 20, Issue:2
Synthesis and topical antiinflammatory properties of 17,21-bis(acetyloxy)-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione and related 2-halogenated compounds.
AID1133646Mineralocorticoid activity in rat assessed as sodium retention up to 1 mg/kg, sc1977Journal of medicinal chemistry, Feb, Volume: 20, Issue:2
Synthesis and topical antiinflammatory properties of 17,21-bis(acetyloxy)-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione and related 2-halogenated compounds.
AID1133645Thymolytic activity in po dosed rat assessed as inhibition of thymus weight administered bid for 7 days1977Journal of medicinal chemistry, Feb, Volume: 20, Issue:2
Synthesis and topical antiinflammatory properties of 17,21-bis(acetyloxy)-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione and related 2-halogenated compounds.
AID1133644Antiinflammatory activity in po dosed rat assessed as inhibition of cotton pellet-induced granuloma weight administered bid for 7 days1977Journal of medicinal chemistry, Feb, Volume: 20, Issue:2
Synthesis and topical antiinflammatory properties of 17,21-bis(acetyloxy)-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione and related 2-halogenated compounds.
AID1133642Antiinflammatory activity in rat assessed as inhibition of cotton pellet-induced granuloma weight administered topically measured per pellet1977Journal of medicinal chemistry, Feb, Volume: 20, Issue:2
Synthesis and topical antiinflammatory properties of 17,21-bis(acetyloxy)-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione and related 2-halogenated compounds.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (15)

TimeframeStudies, This Drug (%)All Drugs %
pre-199014 (93.33)18.7374
1990's1 (6.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.49

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.49 (24.57)
Research Supply Index2.77 (2.92)
Research Growth Index4.27 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.49)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (6.67%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other14 (93.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]