Page last updated: 2024-11-07

proxodolol

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

Description

proxodolol: structure given in first source (3-methoxy- instead of 3-methyl-; text of article gives name as 3-methyl-; see also article on page 27 of the same source) [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID133047
MeSH IDM0234576

Synonyms (11)

Synonym
proxodolol
1-(tert-butylamino)-3-[2-[(3-methoxy-1,2,4-oxadiazol-5-yl)methoxy]phenoxy]propan-2-ol
unii-95n3wb936t
(+/-)-1-(2-((3-methoxy-1,2,4-oxadiazol-5-yl)methoxy)phenoxy)-3-((tert-butylamino))propan-2-ol
zoleprodolol [inn]
158599-53-2
95n3wb936t ,
zoleprodolol
(+/-)-1-(2-((3-methoxy-1,2,4-oxadiazol-5-yl)methoxy)phenoxy)-3-(tert-butylamino)propan-2-ol
Q27271805
AKOS040754576

Research Excerpts

Toxicity

Proxodolol is effective and safe in hypertension. In a dose 120 mg its activity is the same as carvedilol in a dose 25 mg.

ExcerptReferenceRelevance
"The trial demonstrates that proxodolol is highly effective and safe in the treatment of AH."( [Efficacy and safety of the first made in Russia αβ long-acting adrenoblocker proxodolol in patients with arterial hypertension of the second degree].
Beliaeva, SA, 2011
)
0.37
"Proxodolol is effective and safe in hypertension, in a dose 120 mg its activity is the same as carvedilol in a dose 25 mg."( [Efficacy and safety of the first made in Russia αβ long-acting adrenoblocker proxodolol in patients with arterial hypertension of the second degree].
Beliaeva, SA, 2011
)
0.37

Dosage Studied

ExcerptRelevanceReference
"To study efficacy and safety of a new dose and dosage form of proxodolol--a beta-adrenoblocker with alpha1-adrenoblocking activity--in patients with moderate arterial hypertension (AH)."( [Efficacy and safety of the first made in Russia αβ long-acting adrenoblocker proxodolol in patients with arterial hypertension of the second degree].
Beliaeva, SA, 2011
)
0.37
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (4)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)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 (%)
Trials8 (44.44%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other10 (55.56%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]