Landipirdine

CAS No. 1000308-25-7

Landipirdine( RO-5025181 | SYN-120 )

Catalog No. M10003 CAS No. 1000308-25-7

A novel 5-HT receptor antagonist for the treatment of Parkinson's disease.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 561 In Stock
10MG 753 In Stock
25MG 1216 In Stock
50MG 1516 In Stock
100MG 2158 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Landipirdine
  • Note
    Research use only, not for human use.
  • Brief Description
    A novel 5-HT receptor antagonist for the treatment of Parkinson's disease.
  • Description
    A novel 5-HT receptor antagonist for the treatment of Parkinson's disease.Parkinson's DiseasePhase 2 Clinical.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    RO-5025181 | SYN-120
  • Pathway
    GPCR/G Protein
  • Target
    5-HT Receptor
  • Recptor
    5-HT Receptor
  • Research Area
    Neurological Disease
  • Indication
    Parkinson Disease

Chemical Information

  • CAS Number
    1000308-25-7
  • Formula Weight
    362.419
  • Molecular Formula
    C18H19FN2O3S
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O=C(N)NC[C@@H]1CCCC2=C1C=CC(S(=O)(C3=CC=CC(F)=C3)=O)=C2
  • Chemical Name
    N-(((1R)-6-(3-fluorobenzenesulfonyl)-1,2,3,4-tetrahydronaphthalen-1-yl)methyl)urea

Shipping & Storage Information

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

Reference

1. Huot P, et al. ACS Chem Neurosci. 2017 May 17;8(5):973-986.
molnova catalog
related products
  • BF-1

    BF-1 is a novel selective 5-HT2 receptor antagonist that acts by blocking neurogenic dural plasma protein extravasation induced by mCPP or BW723C86.BF-1 is used in the study of migraine.

  • Org-13011 fumarate

    Org-13011 fumarate1 is an agonist of the 5-HT1A receptor and can be used to study neurological disorders.

  • MDL 100907

    A potent, selective 5-HT2A receptor antagonist with Ki of 0.36 nM, > 80-fold selectivity for 5-HT2A over other serotonergic receptors.