Page last updated: 2024-12-06
cortivazol
Description
Research Excerpts
Clinical Trials
Roles
Classes
Pathways
Study Profile
Bioassays
Related Drugs
Related Conditions
Protein Interactions
Research Growth
Market Indicators
Description
cortivazol: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
---|---|
PubMed CID | 66249 |
CHEMBL ID | 2105842 |
CHEBI ID | 135820 |
SCHEMBL ID | 4875 |
MeSH ID | M0047799 |
Synonyms (37)
Synonym |
---|
nsc-80998 |
cortivazol |
1110-40-3 |
D03594 |
cortivazol (usan) |
cortivazolum [inn-latin] |
cortivazol [usan:inn] |
einecs 214-175-8 |
11beta,17alpha,21-trihydroxy-6,16alpha-dimethyl-2'-phenylpregna-2,4,6-trieno(3,2-c)pyrazol-20-one 21-acetate |
2'h-pregna-2,4,6-trieno(3,2-c)pyrazol-20-one, 21-(acetyloxy)-11,17-dihydroxy-6,16-dimethyl-2'-phenyl-, (11beta,16alpha)- |
nsc 80998 |
cortivasolo [dcit] |
11beta,17,21-trihydroxy-6,16alpha-dimethyl-2'-phenyl-2'h-pregna-2,4,6-trieno(3,2-c)pyrazol-20-one 21-acetate |
2'h-pregna-2,4,6-trieno(3,2-c)pyrazol-20-one, 11beta,17,21-trihydroxy-6,16alpha-dimethyl-2'-phenyl-, 21-acetate |
corticoid |
CHEBI:135820 |
ym183k0h63 , |
altim |
unii-ym183k0h63 |
cortivasolo |
CHEMBL2105842 |
cortivazol [mi] |
2'h-pregna-2,4,6-trieno(3,2-c)pyrazol-20-one, 21-(acetyloxy)-11,17-dihydroxy-6,16-dimethyl-2'-phenyl-, (11.beta.,16.alpha.)- |
cortivazol [who-dd] |
cortivazol [mart.] |
11.beta.,17,21-trihydroxy-6,16.alpha.-dimethyl-2'-phenyl-2'h-pregna-2,4,6-trieno(3,2-c)pyrazol-20-one 21-acetate |
cortivazol [usan] |
cortivazol [inn] |
SCHEMBL4875 |
RKHQGWMMUURILY-UHRZLXHJSA-N |
DTXSID40149442 |
11,17,21-trihydroxy-6,16-dimethyl-2-phenyl-2-pregna-2,4,6-trieno[3,2-c]pyrazol-20-one 21-acetate |
DB13003 |
EX-A7287 |
Q2421270 |
[2-[(1s,2r,13s,14s,16r,17r,18s,20s)-17,20-dihydroxy-2,11,16,18-tetramethyl-7-phenyl-6,7-diazapentacyclo[11.7.0.02,10.04,8.014,18]icosa-4(8),5,9,11-tetraen-17-yl]-2-oxoethyl] acetate |
AKOS040746721 |
Research Excerpts
Overview
Cortivazol (CVZ) is a unique, high potency synthetic glucocorticoid. Has a phenylpyrazol fused to the A-ring of the steroid nucleus and displays binding consistent with two or more sites in the cytosol.
Excerpt | Reference | Relevance |
---|---|---|
"Cortivazol is a phenylpyrazolo glucocorticoid of high potency and unusual structure. " | ( Cortivazol mediated induction of glucocorticoid receptor messenger ribonucleic acid in wild-type and dexamethasone-resistant human leukemic (CEM) cells. Ashraf, J; Chilton, D; Kunapuli, S; Thompson, EB, 1991) | 3.17 |
"Cortivazol (CVZ) is a unique, high potency synthetic glucocorticoid, which has a phenylpyrazol fused to the A-ring of the steroid nucleus and displays binding consistent with two or more sites in the cytosol from CEM C7 cells (a human acute lymphoblastic T-cell line)." | ( Two glucocorticoid binding sites on the human glucocorticoid receptor. Srivastava, D; Thompson, EB, 1990) | 1 |
Effects
Excerpt | Reference | Relevance |
---|---|---|
"Cortivazol has potent antileukemic activity in childhood ALL. " | ( Cytotoxicity of cortivazol in childhood acute lymphoblastic leukemia. Kurylak, A; Styczynski, J; Wysocki, M, ) | 1.92 |
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
Drug Classes (1)
Class | Description |
---|---|
steroid | Any of naturally occurring compounds and synthetic analogues, based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred. Natural steroids are derived biogenetically from squalene which is a triterpene. |
[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 (34)
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 8 (23.53) | 18.7374 |
1990's | 13 (38.24) | 18.2507 |
2000's | 10 (29.41) | 29.6817 |
2010's | 3 (8.82) | 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: 34.35
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 moderate demand-to-supply ratio for research on this compound.
| This Compound (34.35) All Compounds (24.57) |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 6 (15.38%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 8 (20.51%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 25 (64.10%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Clinical Trials (3)
Trial Overview
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Plantar Fasciitis Treatment: Double Blinded Randomized Control Study of the Efficacy of an Injection of Platelet Rich Plasma (PRP) Versus an Infiltration of Corticosteroids [NCT03857334] | 50 participants (Actual) | Interventional | 2016-07-01 | Completed | |||
A Double Blind Randomized Controlled Trial of Greater Occipital Nerve Infiltration in Cluster Headache [NCT00804895] | Phase 2/Phase 3 | 43 participants (Actual) | Interventional | 2008-12-31 | Completed | ||
Clinical Results After Medical Therapy Alone or Medical Therapy Associated With Lumbar Traction in the Treatment of Nerve Root Pain of Lumbar Disc Herniation With Disco-radicular Conflict [NCT02793440] | 412 participants (Anticipated) | Interventional | 2013-12-02 | Recruiting | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |