Page last updated: 2024-11-02

4-phenylbutyric acid and Extravascular Hemolysis

4-phenylbutyric acid has been researched along with Extravascular Hemolysis in 1 studies

4-phenylbutyric acid: RN refers to the parent cpd
4-phenylbutyric acid : A monocarboxylic acid the structure of which is that of butyric acid substituted with a phenyl group at C-4. It is a histone deacetylase inhibitor that displays anticancer activity. It inhibits cell proliferation, invasion and migration and induces apoptosis in glioma cells. It also inhibits protein isoprenylation, depletes plasma glutamine, increases production of foetal haemoglobin through transcriptional activation of the gamma-globin gene and affects hPPARgamma activation.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Collins, AF1
Pearson, HA1
Giardina, P1
McDonagh, KT1
Brusilow, SW1
Dover, GJ1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathy[NCT04937062]Early Phase 150 participants (Anticipated)Interventional2021-03-01Enrolling by invitation
A Phase 1b Sequential Open Label Dose-Ranging Study of Safety, Pharmacokinetics, and Preliminary Activity of Benserazide in Subjects With Beta Thalassemia Intermedia and Sickle Cell Disease[NCT04432623]Phase 1/Phase 236 participants (Anticipated)Interventional2020-10-05Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trials

1 trial available for 4-phenylbutyric acid and Extravascular Hemolysis

ArticleYear
Oral sodium phenylbutyrate therapy in homozygous beta thalassemia: a clinical trial.
    Blood, 1995, Jan-01, Volume: 85, Issue:1

    Topics: Adult; Anemia, Sickle Cell; beta-Thalassemia; Blood Transfusion; Erythropoietin; Female; Fetal Hemog

1995
Oral sodium phenylbutyrate therapy in homozygous beta thalassemia: a clinical trial.
    Blood, 1995, Jan-01, Volume: 85, Issue:1

    Topics: Adult; Anemia, Sickle Cell; beta-Thalassemia; Blood Transfusion; Erythropoietin; Female; Fetal Hemog

1995
Oral sodium phenylbutyrate therapy in homozygous beta thalassemia: a clinical trial.
    Blood, 1995, Jan-01, Volume: 85, Issue:1

    Topics: Adult; Anemia, Sickle Cell; beta-Thalassemia; Blood Transfusion; Erythropoietin; Female; Fetal Hemog

1995
Oral sodium phenylbutyrate therapy in homozygous beta thalassemia: a clinical trial.
    Blood, 1995, Jan-01, Volume: 85, Issue:1

    Topics: Adult; Anemia, Sickle Cell; beta-Thalassemia; Blood Transfusion; Erythropoietin; Female; Fetal Hemog

1995