Page last updated: 2024-12-11

ibutamoren mesylate

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

Description

ibutamoren mesylate: a growth hormone secretagogue; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6450830
CHEMBL ID2105872
SCHEMBL ID4451194
MeSH IDM0578056

Synonyms (59)

Synonym
HY-50844
ibutamoren (mesylate)
mk-0677
mk-677
crescendo
l-163191
ibutamoren mesilate
D04491
ibutamoren mesylate (usan)
159752-10-0
ibutamoren mesylate
propanamide, 2-amino-n-(2-(1,2-dihydro-1-(methylsulfonyl)spiro(3h-indole-3,4'-piperidin)-1'-yl)-2-oxo-1-((phenylmethoxy)methyl)ethyl)-2-methyl-, (r)-, monomethanesulfonate
mk 677
mk 0677
r90jb6qj2b ,
2-amino-n-((r)-2-(benzyloxy)-1-((1-(methylsulfonyl)spiro(indoline-3,4'-piperidin)-1'-yl)carbonyl)ethyl)-2-methyl-propionamide monomethanesulfonate
2-amino-n-((r)-2-(benzyloxy)-1-((1-(methylsulfonyl)spiro(indoline-3,4'-piperidin)-1'-yl)carbonyl)ethyl)-2-methylpropionamide monomethanesulfonate
ibutamoren mesylate [usan]
unii-r90jb6qj2b
AKOS015994560
BCP9000829
BCP9000943
BCP0726000081
CS-0444
S1151
CHEMBL2105872
smr004701368
MLS006010300
ibutamoren, mk-0677
ES-0005
2-amino-n-(2-(1,2-dihydro-1-(methylsulfonyl)spiro(3h-indole-3,4'-piperidin)-1'-yl)-2-oxo-1-((phenylmethoxy)methyl)ethyl)-2-methylpropanamide mesilate -l
2-amino-n-(2-(1,2-dihydro-1-(methylsulfonyl)spiro(3h-indole-3,4'-piperidin)-1'-yl)-2-oxo-1-((phenylmethoxy)methyl)ethyl)-2-methylpropanamide mesylate -l
2-amino-n-((r)-2-(benzyloxy)-1-((1-(methylsulphonyl)spiro(indoline-3,4'-piperidin)-1'-yl)carbonyl)ethyl)-2-methylpropionamide monomethanesulphonate
SCHEMBL4451194
1'-(2-methylalanyl-o-benzyl-d-seryl)-1-(methylsulfonyl)-1,2-dihydrospiro[indole-3,4'-piperidine] methanesulfonate (1:1)
2-amino-n-[(1r)-2-[1,2-dihydro-1-(methylsulfonyl)spiro[3h-indole-3,4'-piperidin]-1'-yl]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-2-methylpropanamide methanesulfonate
2-amino-2-methyl-n-[(2r)-1-(1-methylsulfonylspiro[2h-indole-3,4'-piperidine]-1'-yl)-1-oxo-3-(phenylmethoxy)propan-2-yl]propanamide; methanesulfonic acid
(r)-2-amino-n-(3-(benzyloxy)-1-(1-(methylsulfonyl)spiro[indoline-3,4'-piperidin]-1'-yl)-1-oxopropan-2-yl)-2-methylpropanamide methanesulfonate
(r)-2-amino-n-(3-(benzyloxy)-1-(1-(methylsulfonyl)spiro[indoline-3,4'-piperidine]-1'-yl)-1-oxopropan-2-yl)-2-methylpropanamide methanesulfonate
ibutamoren mesylate (mk-677)
J-690213
EX-A728
ibutamorin;mk-677
mfcd00942284
DTXSID50936168
2-amino-n-{3-(benzyloxy)-1-[1-(methanesulfonyl)-1,2-dihydrospiro[indole-3,4'-piperidin]-1'-yl]-1-oxopropan-2-yl}-2-methylpropanimidic acid--methanesulfonic acid (1/1)
propanamide, 2-amino-n-[(1r)-2-[1,2-dihydro-1-(methylsulfonyl)spiro[3h-indole-3,4'-piperidin]-1'-yl]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-2-methyl-, methanesulfonate (1:1)
2-amino-2-methyl-n-[(2r)-1-(1-methylsulfonylspiro[2h-indole-3,4'-piperidine]-1'-yl)-1-oxo-3-phenylmethoxypropan-2-yl]propanamide;methanesulfonic acid
HMS3884A05
CCG-270273
2-amino-2-methyl-n-[(2r)-1-(1-methylsulfonylspiro[2h-indole-3,4'-piperidine]-1'-yl)-1-oxo-3-(phenylmethoxy)propan-2-yl]propanamide mesylate.
Q27287984
2-amino-n-[(1r)-2-[1,2-dihydro-1-(methylsulfonyl)spiro[3h-indole-3,4'-piperidin]-1'-yl]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-2-methylpropanamide methanesulfonate;ibutamoren mesylate
A883281
ibutamoren mesylate (mk-0677)
(r)-2-amino-n-(3-(benzyloxy)-1-(1-(methylsulfonyl)spiro[indoline-3,4'-piperidin]-1'-yl)-1-oxopropan-2-yl)-2-methylpropanamidemethanesulfonate
2-amino-n-(2-(1,2-dihydro-1-(methylsulfonyl)spiro(3h-indole-3,4'-piperidin)-1'-yl)-2-oxo-1-((phenylmethoxy)methyl)ethyl)-2-methylpropanamide mesilate-l
nutrobal
2-amino-n-(2-(1,2-dihydro-1-(methylsulfonyl)spiro(3h-indole-3,4'-piperidin)-1'-yl)-2-oxo-1-((phenylmethoxy)methyl)ethyl)-2-methylpropanamide mesylate-l

Research Excerpts

Overview

Ibutamoren mesylate is an orally active, nonpeptide growth hormone secretagogue. MK-0677 has been developed to stimulate excretion of endogenous growth hormone.

ExcerptReferenceRelevance
"Ibutamoren mesylate, or MK-0677, is an orally active, nonpeptide growth hormone secretagogue that has been developed to stimulate excretion of endogenous growth hormone. "( Equine metabolism of the growth hormone secretagogue MK-0677 in vitro and in urine and plasma following oral administration.
Cutler, C; Habershon-Butcher, J; Taylor, P; Van Eenoo, P; Viljanto, M, 2022
)
2.16

Dosage Studied

ExcerptRelevanceReference
" Serum IGF-I levels were significantly increased over control levels at all dosage levels by 480 min on the first day of MK-0677 administration."( Repeat administration of the GH secretagogue MK-0677 increases and maintains elevated IGF-I levels in beagles.
Chen, HY; Feeney, W; Frazier, E; Hickey, GJ; Jacks, TM; Krupa, D; Nargund, RP; Patchett, AA; Schleim, KD; Smith, RG, 1997
)
0.3
"3 micrograms/L after a week of dosing compared with placebo treatment peak GH values of approximately 9 (treatment day 1) and approximately 7 micrograms/L (treatment day 7)."( MK-677, an orally active growth hormone secretagogue, reverses diet-induced catabolism.
Clemmons, DR; Gertz, BJ; He, W; Murphy, MG; Plunkett, LM; Polvino, WM; Wittreich, J, 1998
)
0.3
" A group of 4 dogs were dosed orally with MK-0677 (5 mg/kg/day) dissolved in deionized water."( Insulin-like growth factor-1 and growth hormone (GH) levels in canine cerebrospinal fluid are unaffected by GH or GH secretagogue (MK-0677) administration.
Block, G; Cahill, M; DeBurlet, G; Handt, L; Hoe, CM; Prahalada, S; van Zwieten, MJ,
)
0.13
" In conclusion, once daily dosing with MK-677, an orally active GH secretagogue, stimulates bone turnover in elderly subjects based on elevations in biochemical markers of bone resorption and formation."( Oral administration of the growth hormone secretagogue MK-677 increases markers of bone turnover in healthy and functionally impaired elderly adults. The MK-677 Study Group.
Bach, MA; Bolognese, J; Cerchio, K; Gertz, BJ; Krupa, D; Murphy, MG; Ng, J; Plotkin, D, 1999
)
0.3
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (100)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's42 (42.00)18.2507
2000's42 (42.00)29.6817
2010's9 (9.00)24.3611
2020's7 (7.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 36.41

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 strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index36.41 (24.57)
Research Supply Index4.80 (2.92)
Research Growth Index4.47 (4.65)
Search Engine Demand Index52.19 (26.88)
Search Engine Supply Index2.04 (0.95)

This Compound (36.41)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials19 (18.63%)5.53%
Reviews23 (22.55%)6.00%
Case Studies1 (0.98%)4.05%
Observational0 (0.00%)0.25%
Other59 (57.84%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]