LTI-291

CAS No. 1919820-28-2

LTI-291( LTI-291 | LTI 291 | LTI291 )

Catalog No. M18176 CAS No. 1919820-28-2

LTI-291 is a glucocerebrosidase (Gcase) activator.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 53 In Stock
5MG 87 In Stock
10MG 147 In Stock
25MG 295 In Stock
50MG 475 In Stock
100MG 692 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    LTI-291
  • Note
    Research use only, not for human use.
  • Brief Description
    LTI-291 is a glucocerebrosidase (Gcase) activator.
  • Description
    LTI-291 is a glucocerebrosidase (Gcase) activator for treatment of Parkinson's disease (PD).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    LTI-291 | LTI 291 | LTI291
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    β-glucosidase
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    1919820-28-2
  • Formula Weight
    358.49
  • Molecular Formula
    C20H30N4O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 50 mg/mL 139.48 mM;
  • SMILES
    O=C(C1=C2N=C(C)C=C(C)N2N=C1)N[C@H]3CC[C@H](OCCCCC)CC3
  • Chemical Name
    5,7-Dimethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (trans-4-pentyloxy-cyclohexyl)-amide

Shipping & Storage Information

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

Reference

1.Renato T. Skerlj, et al. Methods of treatment and combination therapies using gcase activator heterobicyclic and related compounds. WO 2017192841 A1.
molnova catalog
related products
  • [D-Phe12]-Bombesin

    [D-Phe12]-Bombesin is a derivative of Bombesin and an antagonist for bombesin receptor with Ki of 4.7 μM. [D-Phe12]-Bombesin inhibits the Bombesin -induced amylase release, with IC50 of 4 μM.

  • Glycyrrhizinic acid ...

    Glycyrrhizinic acid potassium salt?can reduce ventricular arrhythmias caused by veratrol.

  • ELA-21 (human)

    High affinity apelin receptor agonist. Binds apelin receptors in left ventricle from normal and pulmonary arterial hypertensive (PAH) hearts (pKi values are 9.31 and 9.46, respectively). Bioactive fragment of ELA-32. Inhibits forskolin-induced cAMP production and stimulates β-arrestin recruitment in vitro.