Almotriptan Malate

CAS No. 181183-52-8

Almotriptan Malate ( PNU 180638E )

Catalog No. M12781 CAS No. 181183-52-8

Almotriptan Malate is a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist, used for the treatment of Migraine attacks in adults.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 35 In Stock
25MG 67 In Stock
50MG 124 In Stock
100MG 200 In Stock
500MG 498 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Almotriptan Malate
  • Note
    Research use only, not for human use.
  • Brief Description
    Almotriptan Malate is a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist, used for the treatment of Migraine attacks in adults.
  • Description
    Almotriptan Malate is a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist, used for the treatment of Migraine attacks in adults.
  • Synonyms
    PNU 180638E
  • Pathway
    Endocrinology/Hormones
  • Target
    5-HT Receptor
  • Recptor
    5-HT1B/1D
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    181183-52-8
  • Formula Weight
    469.55
  • Molecular Formula
    C17H25N3O2S·C4H6O5
  • Purity
    >98%(HPLC)
  • Solubility
    Ethanol: 53 mg/mL (112.87 mM); DMSO: 94 mg/mL (200.19 mM)
  • SMILES
    CN(CCC1=CNC2=C1C=C(CS(=O)(N3CCCC3)=O)C=C2)C.O=C(O)C(O)CC(O)=O
  • Chemical Name
    N,N-dimethyl-2-(5-((pyrrolidin-1-ylsulfonyl)methyl)-1H-indol-3-yl)ethan-1-amine 2-hydroxysuccinate

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Pindolol

    Pindolol is a nonselective β-blocker with partial beta-adrenergic receptor agonist activity, also functions as a 5-HT1A receptor weak partial agonist / antagonist (Ki=33nM).

  • WAY-100635

    A potent and selective 5-HT1A receptor antagonist; also acts as potent full agonist at the D4 receptor.

  • YL0919

    An orally active, dual 5-HT1A agonist and selective serotonin reuptake inhibitor with Ki of 0.19 nM and IC50 of 1.78 nM, respectively.