Macimorelin Acetate structure
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Common Name | Macimorelin Acetate | ||
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CAS Number | 381231-18-1 | Molecular Weight | 474.555 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 948.6±65.0 °C at 760 mmHg | |
Molecular Formula | C26H30N6O3 | Melting Point | N/A | |
MSDS | N/A | Flash Point | 527.5±34.3 °C |
Use of Macimorelin AcetateMacimorelin (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)[1][2][3]. |
Name | 2-amino-N-[(2R)-1-[[(1R)-1-formamido-2-(1H-indol-3-yl)ethyl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]-2-methylpropanamide |
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Synonym | More Synonyms |
Description | 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)[1][2][3]. |
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Related Catalog | |
Target |
GHSR[1] |
In Vivo | Macimorelin (5 mg/kg, i.p. twice daily for 2 weeks) decreases the number and duration of seizures in IHKA mouse model[2]. Animal Model: Intrahippocampal kainic acid (IHKA) mouse model[2] Dosage: 5 mg/kg Administration: Intraperitoneal injection (i.p.), twice daily for 2 weeks. Result: Significantly decreased the number and duration of seizures during the treatment period, but had no antiepileptogenic or disease-modifying effect. |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 948.6±65.0 °C at 760 mmHg |
Molecular Formula | C26H30N6O3 |
Molecular Weight | 474.555 |
Flash Point | 527.5±34.3 °C |
Exact Mass | 474.237946 |
PSA | 151.88000 |
LogP | 2.64 |
Vapour Pressure | 0.0±0.3 mmHg at 25°C |
Index of Refraction | 1.676 |
2-Methylalanyl-N-[(1R)-1-formamido-2-(1H-indol-3-yl)ethyl]-D-tryptophanamide |
JMV 1843 |
Macimorelin |
UNII-8680B21W73 |
D-Tryptophanamide, 2-methylalanyl-N-[(1R)-1-(formylamino)-2-(1H-indol-3-yl)ethyl]- |
AEZS-130 |
Macimorelin Acetate |