LY344864
CAS No. 186544-26-3
LY344864( LY-344864 | LY344864 | LY-344864 HCl )
Catalog No. M17398 CAS No. 186544-26-3
LY344864, a specifc receptor agonist, is an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 31 | In Stock |
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5MG | 50 | In Stock |
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10MG | 80 | In Stock |
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25MG | 152 | In Stock |
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50MG | 281 | In Stock |
|
100MG | 500 | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameLY344864
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NoteResearch use only, not for human use.
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Brief DescriptionLY344864, a specifc receptor agonist, is an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor.
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DescriptionLY344864 is a selective 5-HT1F receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. LY344864 possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined. LY344864 was shown to be a full agonist producing an effect similar in magnitude to serotonin itself.
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In VitroLY 344864 binds to human 5-HT1F, 5-HT1A, 5-HT1B, 5-HT1D, 5-HT1E, 5-HT3A, 5-HT2B, 5-HT2C, 5-HT7, rat α1-adrenergic, rat α2-adrenergic receptors with Kis of 0.006, 0.530, 0.549, 0.575, 1.415, 3.935, 1.695, 3.499, 4.851, 5.06 and 3.69 μM, respectively.LY 344864 is a inducer of mitochondrial biogenesis.
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In VivoLY 344864 (0-10 ng/kg; p.o. or i.v.; once) inhibits neurogenic dural inflammation in rat migraine pain model.LY 344864 (1 mg/kg; i.v.; once) can cross the blood brain barrier to some extent in rats.LY 344864 (2 mg/kg; i.p.; daily for 14 days) attenuates dopaminergic neuron loss and improved behavioral endpoints in a Parkinson’s disease mouse model. Animal Model:Male Wistar rats, migraine pain modelDosage:1-10 ng/kg (oral), 0.3-2 ng/kg (intravenous)Administration:Oral, 75 minutes before trigeminal stimulation or intravenous, 10 minutes before trigeminal stimulationResult:When given intravenously 10 minutes before stimulation, inhibited inflammation with an ID50 (median infective dose) of 0.6 ng/kg. When administered orally 75 minutes before trigeminal stimulation, an ID50 of 1.2 ng/kg was obtained.Animal Model:Male C57BL/6 mice, Parkinson’s disease modelDosage:2 mg/kg Administration:Intraperitoneal injection, daily for 14d beginning 7d post-lesion Result:Attenuated TH-ir loss in the striatum and substantia nigra compared to vehicle-treated lesioned animals, also increased locomotor activity in 6-hydroxydopamine lesioned mice, while vehicle treatment had no effect.
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SynonymsLY-344864 | LY344864 | LY-344864 HCl
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PathwayAngiogenesis
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TargetFGFR
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Recptor5-HT1F
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number186544-26-3
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Formula Weight351.42
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Molecular FormulaC21H22FN3O
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Purity>98% (HPLC)
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SolubilityDMSO : ≥ 350 mg/mL; 995.96 mM
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SMILESCN(C)[C@@H]1CCc2c(C1)c1c([nH]2)ccc(c1)NC(=O)c1ccc(cc1)F.Cl
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Chemical NameN-[(3R)-3-(Dimethylamino)-2,3,4,9-tetrahydro-1H-carbazol-6-yl]-4-fluorobenzamide hydrochloride
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Phebus LA, et al. Life Sci. 1997;61(21):2117-26.
molnova catalog
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