Page last updated: 2024-12-07
pyrazinobutazone
Description
Research Excerpts
Clinical Trials
Roles
Classes
Pathways
Study Profile
Bioassays
Related Drugs
Related Conditions
Protein Interactions
Research Growth
Market Indicators
Description
pyrazinobutazone: antipyrene derivative which has anti-inflammatory properties; minor descriptor (75-86); on-line & INDEX MEDICUS search PHENYLBUTAZONE/AA (75-86); RN given refers to phenylbutazone compounded with piperazine [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
---|---|
PubMed CID | 78682 |
CHEMBL ID | 3137687 |
MeSH ID | M0263302 |
Synonyms (23)
Synonym |
---|
unii-0j1026h8ub |
0j1026h8ub , |
1,2-diphenyl-3,5-dioxo-4-n-butylpyrrazolidine de piperazine |
ranoroc |
4-butyl-1,2-diphenylpyrazolidine-3,5-dione, compound with piperazine (1:1) |
carudol |
pyrasanone |
1,2-diphenyl-3,5-dioxo-4-n-butylpyrrazolidine de piperazine [french] |
db 139 |
einecs 225-639-4 |
pyrazinobutazone |
4985-25-5 |
CHEMBL3137687 |
phenylbutazone-piperazine |
phenylbutazone piperazine salt [mi] |
phenylbutazone-piperazine [who-dd] |
phenylbutazone piperazine |
DTXSID60198119 |
4-butyl-1,2-diphenylpyrazolidine-3,5-dione compound with piperazine (1:1) |
4-butyl-1,2-diphenylpyrazolidine-3,5-dione;piperazine |
Q27236841 |
4-butyl-1,2-diphenylpyrazolidine-3,5-dione, compound with piperazine (1 |
AKOS040747320 |
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
Bioassays (19)
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1079936 | Choleostatic liver toxicity, either proven histopathologically or where the ratio of maximal ALT or AST activity above normal to that of Alkaline Phosphatase is < 2 (see ACUTE). Value is number of references indexed. [column 'CHOLE' in source] | |||
AID1079943 | Malignant tumor, proven histopathologically. Value is number of references indexed. [column 'T.MAL' in source] | |||
AID1079935 | Cytolytic liver toxicity, either proven histopathologically or where the ratio of maximal ALT or AST activity above normal to that of Alkaline Phosphatase is > 5 (see ACUTE). Value is number of references indexed. [column 'CYTOL' in source] | |||
AID1079949 | Proposed mechanism(s) of liver damage. [column 'MEC' in source] | |||
AID1079940 | Granulomatous liver disease, proven histopathologically. Value is number of references indexed. [column 'GRAN' in source] | |||
AID1079937 | Severe hepatitis, defined as possibly life-threatening liver failure or through clinical observations. Value is number of references indexed. [column 'MASS' in source] | |||
AID1079948 | Times to onset, minimal and maximal, observed in the indexed observations. [column 'DELAI' in source] | |||
AID1079934 | Highest frequency of acute liver toxicity observed during clinical trials, expressed as a percentage. [column '% AIGUE' in source] | |||
AID1079932 | Highest frequency of moderate liver toxicity observed during clinical trials, expressed as a percentage. [column '% BIOL' in source] | |||
AID1079946 | Presence of at least one case with successful reintroduction. [column 'REINT' in source] | |||
AID1079933 | Acute liver toxicity defined via clinical observations and clear clinical-chemistry results: serum ALT or AST activity > 6 N or serum alkaline phosphatases activity > 1.7 N. This category includes cytolytic, choleostatic and mixed liver toxicity. Value is | |||
AID1079938 | Chronic liver disease either proven histopathologically, or through a chonic elevation of serum amino-transferase activity after 6 months. Value is number of references indexed. [column 'CHRON' in source] | |||
AID1079947 | Comments (NB not yet translated). [column 'COMMENTAIRES' in source] | |||
AID1079941 | Liver damage due to vascular disease: peliosis hepatitis, hepatic veno-occlusive disease, Budd-Chiari syndrome. Value is number of references indexed. [column 'VASC' in source] | |||
AID1079945 | Animal toxicity known. [column 'TOXIC' in source] | |||
AID1079942 | Steatosis, proven histopathologically. Value is number of references indexed. [column 'STEAT' in source] | |||
AID1079931 | Moderate liver toxicity, defined via clinical-chemistry results: ALT or AST serum activity 6 times the normal upper limit (N) or alkaline phosphatase serum activity of 1.7 N. Value is number of references indexed. [column 'BIOL' in source] | |||
AID1079939 | Cirrhosis, proven histopathologically. Value is number of references indexed. [column 'CIRRH' in source] | |||
AID1079944 | Benign tumor, proven histopathologically. Value is number of references indexed. [column 'T.BEN' in source] | |||
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Research
Studies (7)
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 6 (85.71) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (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: 11.72
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.
| This Compound (11.72) All Compounds (24.57) |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 3 (33.33%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 3 (33.33%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 3 (33.33%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |