Page last updated: 2024-09-25

brl 35135

Description

BRL 35135: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID122186
CHEMBL ID49289
SCHEMBL ID4611391
MeSH IDM0174460

Synonyms (14)

Synonym
brl35135a
methyl 4-(2-(2-hydroxy-2-(3-chlorophenyl)ethylamino)propyl)phenoxyacetate
brl 35135
acetic acid, (4-(2-((2-(3-chlorophenyl)-2-hydroxyethyl)amino)propyl)phenoxy)-, methyl ester
CHEMBL49289
L003499
91097-81-3
SCHEMBL4611391
n-[2-(4-carbomethoxymethoxyphenyl)-1-methylethyl]-2-hydroxy-2-(3-chlorophenyl) ethanamine
methyl 4-[2-[(3-chloro-beta-hydroxyphenethyl) amino]propyl]phenoxyacetate
ZFLBZHXQAMUEFS-UHFFFAOYSA-N
4-[2-(2-(3-chlorophenyl)-2-hydroxyethylamino)propyl]phenoxya cetic acid methyl ester
DTXSID90919975
methyl [4-(2-{[2-(3-chlorophenyl)-2-hydroxyethyl]amino}propyl)phenoxy]acetate

Research Excerpts

Overview

ExcerptReference
"BRL 35135 is a novel oral agent which, when dosed chronically to obese rodents with abnormal glucose tolerance, improves both insulin sensitivity and glucose tolerance. "( Cawthorne, MA; Ellis, RD; Mitchell, TH; Robb, G; Smith, SA, 1989)

Treatment

ExcerptReference
"BRL 35135 treatment doubled BAT uncoupling protein mRNA levels (p < 0.05), and increased core temperature by 0.4 degree C (p < 0.05), but neither hypothalamic regional NPY levels nor hypothalamic NPY mRNA levels were affected by BRL 35135."( Bing, C; Buckingham, R; Frankish, H; Hopkins, D; Wang, Q; Williams, G, 1998)
"BRL 35135 treatment increased expression levels of beta3-AR mRNA in both genotypes."( Cawthorne, MA; Emilsson, V; Hamilton, S; Liu, YL; Summers, RJ, 1998)
"3. Treatment with BRL 35135 reduced weight gain by 19%, increased brown adipose tissue thermogenic activity 45-fold and reduced plasma insulin by 50%."( Hänninen, V; Huupponen, R; Jhanwar-Uniyal, M; Koulu, M; Pesonen, U; Rouru, J; Santti, E, 1994)

Bioassays (4)

Assay IDTitleYearJournalArticle
AID235309Ratio of the dose raising the rat heart rate to 500bpm, to ED50 for inhibition of GDP binding to beta-3 adrenergic receptor1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Selective beta 3-adrenergic agonists of brown adipose tissue and thermogenesis. 1. [4-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethoxy]phenoxy]acetates.
AID41942Inhibition of beta-3 adrenergic receptor GDP binding in rat brown adipose tissue on oral administration relative to isoprenaline1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Selective beta 3-adrenergic agonists of brown adipose tissue and thermogenesis. 1. [4-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethoxy]phenoxy]acetates.
AID41943Dose necessary to produce 50% of the isoprenaline effect to inhibit GDP binding to beta-3 adrenergic receptor in brown adipose tissue (BAT mitochondria) of rats after subcutaneous administration.1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Selective beta 3-adrenergic agonists of brown adipose tissue and thermogenesis. 1. [4-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethoxy]phenoxy]acetates.
AID235307Ratio of the dose (D500,peroral administration) elevating the rat heart rate to 500 bpm to the GDP ED50.1992Journal of medicinal chemistry, May-15, Volume: 35, Issue:10
Selective beta 3-adrenergic agonists of brown adipose tissue and thermogenesis. 1. [4-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethoxy]phenoxy]acetates.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (38)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (2.63)18.7374
1990's32 (84.21)18.2507
2000's4 (10.53)29.6817
2010's1 (2.63)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 (%)
Trials3 (7.89%)5.53%
Reviews1 (2.63%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other34 (89.47%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research Highlights

Long-term Use (2)

ArticleYear
Contrasts between the effects of zinc-α2-glycoprotein, a putative β3/2-adrenoceptor agonist and the β3/2-adrenoceptor agonist BRL35135 in C57Bl/6 (ob/ob) mice.
The Journal of endocrinology, Volume: 216, Issue: 2
2013
Effect of the beta-adrenoceptor agonist BRL-35135 on development of obesity in suckling Zucker (fa/fa) rats.
The American journal of physiology, Volume: 268, Issue: 6 Pt 1
1995
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Dosage (5)

ArticleYear
Contrasts between the effects of zinc-α2-glycoprotein, a putative β3/2-adrenoceptor agonist and the β3/2-adrenoceptor agonist BRL35135 in C57Bl/6 (ob/ob) mice.
The Journal of endocrinology, Volume: 216, Issue: 2
2013
Desensitization of beta3-adrenergic receptor-stimulated adenylyl cyclase activity and lipolysis in rats.
Life sciences, Volume: 62, Issue: 7
1998
Thermoregulatory responses to beta-adrenergic agonists at low ambient temperatures in the rat.
Experimental physiology, Volume: 78, Issue: 6
1993
Effects of beta-adrenoceptor agonists and antagonists on thermoregulation in the cold in lean and obese Zucker rats.
Pharmacology, biochemistry, and behavior, Volume: 46, Issue: 4
1993
Effects of BRL 35135, a beta-adrenoceptor agonist with novel selectivity, on glucose tolerance and insulin sensitivity in obese subjects.
International journal of obesity, Volume: 13, Issue: 6
1989
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]