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
5MG 50 In Stock
10MG 80 In Stock
25MG 152 In Stock
50MG 281 In Stock
100MG 500 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    LY344864
  • Note
    Research use only, not for human use.
  • Brief Description
    LY344864, a specifc receptor agonist, is an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor.
  • Description
    LY344864 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.
  • In Vitro
    LY 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.
  • In Vivo
    LY 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.
  • Synonyms
    LY-344864 | LY344864 | LY-344864 HCl
  • Pathway
    Angiogenesis
  • Target
    FGFR
  • Recptor
    5-HT1F
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    186544-26-3
  • Formula Weight
    351.42
  • Molecular Formula
    C21H22FN3O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 350 mg/mL; 995.96 mM
  • SMILES
    CN(C)[C@@H]1CCc2c(C1)c1c([nH]2)ccc(c1)NC(=O)c1ccc(cc1)F.Cl
  • Chemical Name
    N-[(3R)-3-(Dimethylamino)-2,3,4,9-tetrahydro-1H-carbazol-6-yl]-4-fluorobenzamide hydrochloride

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Phebus LA, et al. Life Sci. 1997;61(21):2117-26.
molnova catalog
related products
  • Alofanib

    Alofanib is a selective allosteric inhibitor of FGFR2 and has a dramatic inhibitory effect on FGF2-induced phosphorylation of FRS2a in KATO III cells (IC50 <10 nM).

  • Sunitinib Malate

    Potent, ATP-competitive VEGFR, PDGFRβ and KIT inhibitor.

  • Derazantinib

    Derazantinib (ARQ-087) is a novel potent, ATP competitive multi-kinase inhibitor with IC50 of FGFR1/2/3 with IC50 of 1.8-4.5 nM.