18 Results for "

GHSR agonist

" in MedChemExpress (MCE) Product Catalog:
Products (18)

18 Results for "GHSR agonist" in MCE Product Catalog:

  • Targets Recommended:
5
5 Cited Publications
Cat. No.: HY-50844
CAS No.: 159752-10-0
Synonyms: MK-677; MK-0677
Target:  

GHSR

Research Areas:  

Endocrinology

Ibutamoren Mesylate (MK-677) is a potent, non-peptide Growth hormone secretagogue receptor (GHSR) agonist. Ibutamoren Mesylate is an orally active growth hormone (GH) secretagogue.
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2
2 Cited Publications
Cat. No.: HY-19884B
CAS No.: 2863659-22-5
Synonyms: RM-131 TFA; BIM-28131 TFA
Target:  

GHSR

Research Areas:  

Metabolic Disease

Relamorelin (RM-131) TFA, a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a Ki of 0.42 nM for GHS-1a receptor. Relamorelin TFA is centrally penetrant. Relamorelin TFA increases growth hormone levels and accelerates gastric emptying. Relamorelin TFA has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research .
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Cat. No.: HY-14820A
CAS No.: 945212-59-9
Purity:  98.96%
Synonyms: EP-1572 acetate; AEZS-130 acetate
Target:  

GHSR

Macimorelin (EP-1572) acetate, a GH secretagogue, is an orally active GHSR agonist. Macimorelin acetate stimulates GH release. Macimorelin acetate can be used in the research of adult growth hormone deficiency (AGHD), and Cancer anorexia-cachexia syndrome (CACS) .
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Cat. No.: HY-15243
CAS No.: 193273-69-7
Purity:  98.19%
Synonyms: CP 424391-18
Target:  

GHSR

Research Areas:  

Neurological Disease Endocrinology

Capromorelin Tartrate is an orally active, potent growth hormone secretagogue receptor (GHSR) agonist, with Ki of 7 nM for hGHS-R1a.
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Cat. No.: HY-50760
CAS No.: 145455-35-2
Target:  

GHSR

Research Areas:  

Endocrinology

L-692585 is a potent and nonpeptidyl growth hormone secretagogue receptor (GHS-R1a) agonist, with a Ki of 0.8 nM. L-692585 acts directly on somatotropes causing GH release .
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Cat. No.: HY-14820
CAS No.: 381231-18-1
Synonyms: EP-1572; AEZS-130
Target:  

GHSR

Research Areas:  

Endocrinology Cancer

Macimorelin (EP-1572), a GH secretagogue, is an orally active GHSR agonist. Macimorelin stimulates GH release. Macimorelin can be used in the research of adult growth hormone deficiency (AGHD), and Cancer anorexia-cachexia syndrome (CACS) .
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Cat. No.: HY-19884
CAS No.: 661472-41-9
Synonyms: RM-131; BIM-28131
Target:  

GHSR

Research Areas:  

Metabolic Disease

Relamorelin (RM-131), a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a Ki of 0.42 nM for GHS-1a receptor. Relamorelin is centrally penetrant. Relamorelin increases growth hormone levels and accelerates gastric emptying. Relamorelin has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research .
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Cat. No.: HY-173271
CAS No.: 3060887-25-1
Target:  

GHSR

Research Areas:  

Endocrinology

GHSR-1a agonist-1 (Compound 4b) is an orally active agonist of the human growth hormone secretagogue receptor 1a (GHSR-1a), with an EC50 of 0.49 nM. GHSR-1a agonist-1 can effectively stimulate the release of endogenous growth hormone by activating GHSR-1a. GHSR-1a agonist-1 administered orally at a dose as low as 0.1 mg/kg can increase the body weight and body length of 4-week-old rats. GHSR-1a agonist-1 can be used in the research field of growth and development retardation in children .
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Cat. No.: HY-153095
CAS No.: 2857112-06-0
Target:  

GHSR

Research Areas:  

Metabolic Disease

PF-6870961 is an inverse agonist of GHSR1a with Ki values of 73.6 nM (human GHSR), 239 nM (rat GHSR), and 217 nM (dog GHSR), respectively. PF-6870961 inhibits the constitutive GHSR1a-induced IP accumulation with an IC50 value of 300 nM. PF-6870961 also inhibits constitutive GHSR1a β-arrestin mobilization with an IC50 value of 1.10 nM .
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Cat. No.: HY-137061
CAS No.: 1143020-91-0
Target:  

GHSR

Research Areas:  

Metabolic Disease

AZ-GHS-22 is a potent, non-CNS penetrant GHS-R1a inverse agonist (IC50=0.77 nM) .
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Cat. No.: HY-119125
CAS No.: 295337-71-2
Target:  

GHSR

Research Areas:  

Cancer

BMS-317180 is an orally active and potent growth hormone secretagogue receptor (GHS-R) agonist (EC50=7.9 nM). BMS-317180 stimulates endogenous growth hormone (GH) release. BMS-317180 is promising for research of age-related frailty, osteoporosis, and cancer cachexia .
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Cat. No.: HY-14495
CAS No.: 674343-47-6
Synonyms: EX-1314
Target:  

GHSR

Research Areas:  

Metabolic Disease

BMS-604992 (EX-1314) is a selective, orally active small-molecule growth hormone secretagogue receptor (GHSR) agonist. BMS-604992 demonstrates high-affinity binding (Ki=2.3 nM) and potent functional activity (EC50=0.4 nM). BMS-604992 can stimulate food intake in rodents .
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Cat. No.: HY-19884A
CAS No.: 1809080-14-5
Synonyms: RM-131 acetate; BIM-28131 acetate
Target:  

GHSR

Research Areas:  

Metabolic Disease

Relamorelin (RM-131) acetate, a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a Ki of 0.42 nM for GHS-1a receptor. Relamorelin acetate is centrally penetrant. Relamorelin acetate increases growth hormone levels and accelerates gastric emptying. Relamorelin acetate has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research .
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Cat. No.: HY-115272
CAS No.: 1012035-06-1
Target:  

GHSR

Research Areas:  

Neurological Disease

GSK894490A is a non-peptide ghrelin receptor agonist .
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Cat. No.: HY-153095A
CAS No.: 2857112-07-1
Target:  

GHSR

Research Areas:  

Metabolic Disease

PF-6870961 hydrochloride is an inverse agonist of GHSR1a with Ki values of 73.6 nM (human GHSR), 239 nM (rat GHSR), and 217 nM (dog GHSR), respectively. PF-6870961 hydrochloride inhibits the constitutive GHSR1a-induced IP accumulation with an IC50 value of 300 nM. PF-6870961 hydrochloride also inhibits constitutive GHSR1a β-arrestin mobilization with an IC50 value of 1.10 nM .
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Cat. No.: HY-14495B
CAS No.: 1469750-46-6
Synonyms: EX-1314 dihydrochloride
Target:  

GHSR

Research Areas:  

Metabolic Disease

BMS-604992 (EX-1314) dihydrochloride is a selective, orally active small-molecule growth hormone secretagogue receptor (GHSR) agonist. BMS-604992 dihydrochloride demonstrates high-affinity binding (ki=2.3 nM) and potent functional activity (EC50=0.4 nM). BMS-604992 dihydrochloride can stimulate food intake in rodents .
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Cat. No.: HY-14495A
CAS No.: 760944-56-7
Synonyms: EX-1314 free base
Target:  

GHSR

Research Areas:  

Metabolic Disease

BMS-604992 (EX-1314) free base is a selective, orally active small-molecule growth hormone secretagogue receptor (GHSR) agonist. BMS-604992 free base demonstrates high-affinity binding (ki=2.3 nM) and potent functional activity (EC50=0.4 nM). BMS-604992 free base can stimulate food intake in rodents .
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Cat. No.: HY-176995
CAS No.: 1143021-16-2
Target:  

GHSR

Research Areas:  

Metabolic Disease

AZ-GHS-38 (compound 38) is an orally active CNS-penetrant inverse agonist of growth hormone secretagogue receptor (GHS-R1a) with an IC50 of 6.7 nM. AZ-GHS-38 results in acute reduction of food intake in wild-type mice. AZ-GHS-38 can be used for anti-obesity research .
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