Page last updated: 2024-11-11

ave 0991

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

Description

AVE 0991: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID9851724
CHEMBL ID4303593
SCHEMBL ID15045765
MeSH IDM0443983

Synonyms (28)

Synonym
cid 9851724
1-ethyl-3-[3-[4-[(5-methanoyl-4-methoxy-2-phenyl-imidazol-1-yl)methyl]phenyl]-5-(2-methylpropyl)thiophen-2-yl]sulfonyl-urea
304462-19-9
1-ethyl-3-[[3-[4-[(5-formyl-4-methoxy-2-phenyl-1-imidazolyl)methyl]phenyl]-5-(2-methylpropyl)-2-thiophenyl]sulfonyl]urea
A820377
gtpl5579
3-ethyl-1-[3-[4-[(5-formyl-4-methoxy-2-phenylimidazol-1-yl)methyl]phenyl]-5-(2-methylpropyl)thiophen-2-yl]sulfonylurea
ave 0991
FD5038
ave0991
CS-1752
HY-15778
unii-68jr6nci7i
2-thiophenesulfonamide, n-((ethylamino)carbonyl)-3-(4-((5-formyl-4-methoxy-2-phenyl-1h-imidazol-1-yl)methyl)phenyl)-5-(2-methylpropyl)-
ave-0991
68jr6nci7i ,
n-(ethylcarbamoyl)-3-(4-((5-formyl-4-methoxy-2-phenyl-1h-imidazol-1-yl)methyl)phenyl)-5-isobutylthiophene-2-sulfonamide
SCHEMBL15045765
DTXSID50184526
AKOS027338221
mfcd27992063
Q27074634
BCP11067
1-ethyl-3-[3-[4-[(5-formyl-4-methoxy-2-phenylimidazol-1-yl)methyl]phenyl]-5-(2-methylpropyl)thiophen-2-yl]sulfonylurea
EX-A2901
CHEMBL4303593 ,
AS-55939
bdbm50514584

Research Excerpts

Overview

AVE 0991 (AVE) is a non-peptide compound, mimic of the angiotensin (Ang)-(1-7) actions in many tissues and pathophysiological states.

ExcerptReferenceRelevance
"AVE 0991 (AVE) is a non-peptide compound, mimic of the angiotensin (Ang)-(1-7) actions in many tissues and pathophysiological states. "( AVE 0991, a non-peptide mimic of angiotensin-(1-7) effects, attenuates pulmonary remodelling in a model of chronic asthma.
Caliari, MV; Campagnole-Santos, MJ; Cara, DC; Cardoso, JA; Kangussu, LM; Lautner, RQ; Magalhães, GS; Marques, FD; Murari, A; Noviello, ML; Oliveira, ML; Pereira, JM; Rodrigues-Machado, MG; Santos, RA, 2013
)
3.28

Actions

ExcerptReferenceRelevance
"AVE 0991 did not inhibit plasma Ang-converting enzyme activity in vitro or the pressor effect of Ang I in vivo."( Evidence for Mas-mediated bradykinin potentiation by the angiotensin-(1-7) nonpeptide mimic AVE 0991 in normotensive rats.
Campagnole-Santos, MJ; Carvalho, MB; da Mata Machado, LT; de Paula, RD; Duarte, FV; Faria-Silva, R; Fauler, B; Santos, RA, 2007
)
1.28

Treatment

ExcerptReferenceRelevance
"Treatment with AVE 0991 in 2K1C rats restored the baroreflex sensitivity of both bradycardic and tachycardic components to levels comparable to those of normotensive SHAM rats. "( The nonpeptide ANG-(1-7) mimic AVE 0991 attenuates cardiac remodeling and improves baroreflex sensitivity in renovascular hypertensive rats.
Alzamora, AC; Campagnole-Santos, MJ; Cunha, TM; Lima, WG; Silva, ME; Souza Santos, RA, 2013
)
1.03

Bioavailability

ExcerptReferenceRelevance
"Recently, recombinant angiotensin-converting enzyme 2 was shown to protect mice from acute lung injury, an effect attributed to reduced bioavailability of angiotensin II."( Angiotensin-(1-7) protects from experimental acute lung injury.
Erfinanda, L; Gembardt, F; Kaestle, SM; Klein, N; Kuebler, WM; Lei, X; Mertens, M; Nickles, H; Supé, S; Szaszi, K; Walther, T; Wang, L; Yin, J, 2013
)
0.39
" Interestingly, perivascular adipose tissue (PVAT) and adventitial infiltration with macrophages and T-cells precedes atherosclerotic plaque or the impairment of endothelium-dependent NO bioavailability (a measure of endothelial function)."( Anti-atherosclerotic effect of the angiotensin 1-7 mimetic AVE0991 is mediated by inhibition of perivascular and plaque inflammation in early atherosclerosis.
Czesnikiewicz-Guzik, M; Guzik, TJ; Jawien, J; Korbut, R; Mikolajczyk, TP; Montezano, AC; Nosalski, R; Olszanecki, R; Rios, FJ; Siedlinski, M; Skiba, DS; Touyz, RM, 2017
)
0.46
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Proto-oncogene MasHomo sapiens (human)IC50 (µMol)0.02100.02100.02100.0210AID1560683
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (15)

Processvia Protein(s)Taxonomy
negative regulation of protein phosphorylationProto-oncogene MasHomo sapiens (human)
spermatogenesisProto-oncogene MasHomo sapiens (human)
positive regulation of cell population proliferationProto-oncogene MasHomo sapiens (human)
male gonad developmentProto-oncogene MasHomo sapiens (human)
response to xenobiotic stimulusProto-oncogene MasHomo sapiens (human)
response to activityProto-oncogene MasHomo sapiens (human)
hippocampus developmentProto-oncogene MasHomo sapiens (human)
response to gonadotropinProto-oncogene MasHomo sapiens (human)
angiotensin-activated signaling pathwayProto-oncogene MasHomo sapiens (human)
positive regulation of canonical NF-kappaB signal transductionProto-oncogene MasHomo sapiens (human)
positive regulation of DNA replicationProto-oncogene MasHomo sapiens (human)
regulation of inflammatory responseProto-oncogene MasHomo sapiens (human)
positive regulation of inositol phosphate biosynthetic processProto-oncogene MasHomo sapiens (human)
protein kinase C signalingProto-oncogene MasHomo sapiens (human)
G protein-coupled receptor signaling pathwayProto-oncogene MasHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (5)

Processvia Protein(s)Taxonomy
angiotensin receptor activityProto-oncogene MasHomo sapiens (human)
G protein-coupled receptor activityProto-oncogene MasHomo sapiens (human)
angiotensin type II receptor activityProto-oncogene MasHomo sapiens (human)
protein bindingProto-oncogene MasHomo sapiens (human)
peptide bindingProto-oncogene MasHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (2)

Processvia Protein(s)Taxonomy
plasma membraneProto-oncogene MasHomo sapiens (human)
cell surfaceProto-oncogene MasHomo sapiens (human)
plasma membraneProto-oncogene MasHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1560683Agonist activity at N-terminal c-Myc tagged human MasR expressed in HEK293T cells assessed as reduction in forskolin-induced cAMP accumulation2020Journal of medicinal chemistry, 03-12, Volume: 63, Issue:5
The Other Angiotensin II Receptor: AT
AID1345372Mouse MAS1 (Class A Orphans)2004Hypertension (Dallas, Tex. : 1979), Oct, Volume: 44, Issue:4
Nonpeptide AVE 0991 is an angiotensin-(1-7) receptor Mas agonist in the mouse kidney.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (47)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's10 (21.28)29.6817
2010's27 (57.45)24.3611
2020's10 (21.28)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 27.51

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.

MetricThis Compound (vs All)
Research Demand Index27.51 (24.57)
Research Supply Index3.89 (2.92)
Research Growth Index4.78 (4.65)
Search Engine Demand Index22.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (27.51)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (4.17%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other46 (95.83%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]