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GHSR

Growth hormone secretagogue receptor(GHS-R), also known as ghrelin receptor, is a G protein-coupled receptor that binds growth hormone secretagogues (GHSs), such as ghrelin, the "hunger hormone". The role of GHS-R is thought to be in regulating energy homeostasis and body weight. In the brain, they are most highly expressed in the hypothalamus, specifically the ventromedial nucleus and arcuate nucleus. GSH-Rs are also expressed in other areas of the brain, including the ventral tegmental area, hippocampus, and substantia nigra. Outside the central nervous system, too, GSH-Rs are also found in the liver, in skeletal muscle, and even in the heart.

  • Relamorelin
    T34281661472-41-9在庫ざいこ
    Relamorelin (RM-131), a selective and potent growth hormone-releasing peptide growth hormone secretagogue receptor (GHSR) agonist, is a potent growth hormone-releasing peptide mimetic with a high affinity for the GHS-1a receptor Relamorelin is a centrally permeable pentapeptide that increases growth hormone levels and accelerates gastric emptying and has potential for studying malignant disease.
    • ¥114,000
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  • Ibutamoren Mesylate
    T7112159752-10-0
    Ibutamoren Mesylate (MK-0677) is a potent, non-peptide Growth hormone secretagogue receptor (GHSR) agonist.
    • ¥13,000
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  • Anamorelin
    T10319249921-19-5
    Anamorelin (ONO-7643) is a novel ghrelin receptor agonist (EC50: 0.74 nM in the FLIPR assay).
    • ¥13,000
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  • Cortistatin-8 acetate
    TP2236L
    Cortistatin-8 acetate is a corticosteroid analog, a GHS-R antagonist with inhibitory effects on the growth hormone pro-secretin receptor.Cortistatin-8 acetate is a synthetic corticosteroid-derived ligand for the growth hormone-releasing peptide receptor and does not alter the endocrine response to acylated growth hormone-releasing peptide or hesperidin in humans.Cortistatin-8 acetate is a synthetic corticosteroid-derived ligand for the growth hormone-releasing peptide receptor.
    • ¥55,000
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  • Human growth hormone-releasing factor acetate
    TP1155L
    Human growth hormone-releasing factor acetate is a hypothalamic polypeptide and stimulates GH production and release by binding to the GHRH Receptor (GHRHR) on cells in the anterior pituitary[1].
    • ¥45,500
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  • CJC-1295 acetate(863288-34-0 free base)
    TP2328L
    CJC-1295 acetate(863288-34-0 free base) (DAC:GRF acetate) is a synthetic analogue of growth hormone-releasing hormone (GHRH) (also known as growth hormone-releasing factor (GRF)) and a growth hormone secretagogue (GHS)
    • ¥30,500
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  • Obestatin (rat) acetate
    TP2279L
    Obestatin (rat) acetate is an endogenous ligand of G-protein coupled receptor 39 (GPR39). Obestatin (rat) acetate has anti-inflammatory, anti-myocardial infarction and antioxidant properties. Obestatin (rat) acetate suppresses food intake, inhibits jejunal contraction, and decreases body-weight gain.
    • ¥27,000
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  • NF-56-EJ40 hydrochloride
    T12216L2728500-80-7在庫ざいこ
    NF-56-EJ40 hydrochloride is a potent, high-affinity, and highly selective human SUCNR1 (GPR91) antagonist with an IC50 of 25 nM and a Ki of 33 nM, and shows almost no activity towards rat SUCNR1. NF-56-EJ40 hydrochloride has high affinity for humanized rat SUCNR1 with a Ki value of 17.4 nM.
    • ¥11,500
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  • L-692429
    T11798145455-23-8在庫ざいこ
    L-692429 (MK-0751) is a potent nonpeptidyl growth hormone secretagogue (GHS) agonist and benzolactam derivative, known for reversing glucocorticoid-induced inhibition of GH secretion. L-692429 exhibits high affinity for the G protein-coupled receptor and is useful in studying acromegaly and obesity.
    • ¥36,500
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  • Capromorelin Tartrate
    TQ0022193273-69-7
    Capromorelin Tartrate (CP 424391-18) is a potent, orally active growth hormone secretagogue receptor (GHSR) agonist (Ki: 7 nM for hGHS-R1a).
    • ¥9,000
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  • hGPR91 antagonist 1
    T115601314796-00-3
    hGPR91 antagonist 1 is a potent and selective hGPR91 antagonist (IC50: 7 μみゅーM).
    • ¥20,000
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  • TC-G-1008
    T46481621175-65-2
    TC-G-1008 (GPR39-C3) is a zinc receptor agonist with EC50 values of 0.4 nM for rat GPR39 and 0.8 nM for human GPR39.
    • ¥9,500
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  • JMV 2959 hydrochloride (925238-89-7 free base)
    T117192448414-54-6
    JMV 2959 hydrochloride (925238-89-7 free base) is a growth hormone secretagogue receptor type 1a (GHS-R1a) antagonist with an IC50 of 32±3 nM in LLC-PK1 cells.
    • ¥8,000
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  • Emoghrelin
    T80006928262-58-2
    Emoghrelin, extracted from Heshouwu (Polygonum multiflorum), promotes the secretion of growth hormone by activating the ghrelin receptor [1].
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  • TM-N1324
    T171031144477-35-9
    TM-N1324 is a GPR39 agonist. TM-N1324 activates human GPR39 with high efficacy and potencies of 280 nM and 9 nM in the absence and presence of Zn2+, respectively. TM-N1324 has similar potencies to murine GPR39 with EC50s of 180 nM and 5 nM, respectively.
    • ¥10,000
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  • AnaMorelin hydrochloride
    T7225861998-00-7
    AnaMorelin hydrochloride (RC-1291 hydrochloride) is a novel ghrelin receptor agonist(EC50 : 0.74 nM, in the FLIPR assay).
    • ¥7,000
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  • Pralmorelin
    T5025158861-67-7
    Pralmorelin is an oral active synthetic peptide analogue of MEK. Pralmorelin is an auxin releasing peptide/growth hormone secretory receptor agonist, can selectively stimulate ghrelin receptor and cause growth hormone release, has shown anti-inflammatory activity.
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    • YIL 781
      T23543875258-85-8
      YIL 781 is a selective ghrelin receptor antagonist (GHS-R1a) (Ki = 17 nM), showing a weak affinity for kinesin receptors (K = 6 μみゅーM). YIL 781 improves glucose homeostasis in vivo and in vitro by blocking ghrelin secretion.
      • ¥10,000
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    • PF-5190457
      T165081334782-79-4
      PF-5190457 is an effective and selective ghrelin receptor inverse agonist (pKi: 8.36).
      • ¥7,500
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