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Merck

SML4366

Lasmiditan hemisuccinate

≥98% (HPLC)

Synonym(s):

2,4,6-Trifluoro-N-[6-[(1-methyl-4-piperidinyl)carbonyl]-2-pyridinyl]benzamid hemisuccinate, 2,4,6-Trifluoro-N-[6-[(1-methylpiperidin-4-yl)carbonyl]pyridin-2yl]benzamide hemisuccinate, COL 144 hemisuccinate, COL-144 hemisuccinate, COL144 hemisuccinate, LY 573144 hemisuccinate, LY-573144 hemisuccinate, LY573144 hemisuccinate

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About This Item

Empirical Formula (Hill Notation):
C38H36F6N6O4·C4H6O4
CAS Number:
Molecular Weight:
872.81
UNSPSC Code:
12352200
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
Storage condition:
desiccated
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Quality Level

assay

≥98% (HPLC)

form

powder

drug control

USDEA Schedule V

storage condition

desiccated

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

-10 to -25°C

Biochem/physiol Actions

Lasmiditan (COL-144 and LY573144) is an orally active, potent and selective high-affinity serotonin receptor 5-HT1F agonist (5-HT1F/1E Ki = 2.21/594 nM; 5-HT1A/B/C Ki >1 μM; 5-HT2A/B/C Ki >2 μM; 5-HT6/7 Ki >3 μM). Lasmiditan induces mitochondrial biogenesis (MB) in human glomerular endothelial cells and mouse glomerular endothelial cells (100 nM for 72h). Unlike the triptans, Lasmiditan is void of vasoconstrictor activity toward isolated human coronary arteries (up to 100 μM) or in anaesthetized female beagle dogs in vivo (4.13-11.13 mg/kg i.v.)

Disclaimer

Hygroscopic, Store with desiccant


signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

11 - Combustible Solids



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Global Trade Item Number

SKUGTIN
SML4366-10MG04065273787368
SML4366-50MG04065273787375