• Skip to primary navigation
  • Skip to main content
  • Skip to footer

LKT Labs

Biochemicals for Life Science Research

  • Products
    • New Products
    • Cancer Biology
    • Cardiovascular
    • Endocrine Signaling and Immunology
    • Metabolic and GI Pathology
    • Microbiology
    • Natural Products
    • Neuroscience
    • Peptides
    • Pharmaceutical Impurities and Derivatives
    • Stem Cell Modulators
  • Services
    • Custom Synthesis
    • Natural Product Isolation
    • Analytical Services
  • Int’l Distributors
  • Support
    • About LKT Labs
    • General Inquiry
    • Bulk Quote Request
    • Document Request
    • Technical Support
    • Catalog Request
    • Product Flyers
  • Contact Us
  • Cart
  • Login / Register
YM-201636

YM-201636

Product ID Y4802
Cas No. 371942-69-7
Purity ≥98%
Product Unit SizeCostQuantityStock
1 mg $107.00 In stock
5 mg $274.20 In stock
10 mg $438.80 In stock
Bulk Quote

Quicklinks

  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Custom Order

Description

YM-201636 is an inhibitor of PIKfyve, decreasing the synthesis of phosphatidylinositol 3,5-disphosphate. YM-210636 decreases muscular contraction-stimulated glucose uptake in vitro and induces autophagy-dependent neuronal death in other cellular models. Additionally, YM-210636 inhibits endomembrane transport and retroviral budding in vitro.

Product Info

Cas No.

371942-69-7

Purity

≥98%

Formula

C25H23N7O3

Formula Wt.

469.50

IUPAC Name

6-amino-N-[3-(4-morpholin-4-ylpyrido[2,3]furo[2,4-b]pyrimidin-2-yl)phenyl]pyridine-3-carboxamide

Solubility

DMSO 35 mg/mL (74.86 mM) Water Insoluble Ethanol Insoluble

Appearance

Beige-Yellow Powder

Shipping and Storage

Store Temp

-20°C

Ship Temp

Ambient

Downloads

MSDS

Y4802 MSDS PDF

Info Sheet

Y4802 Info Sheet PDF

References

Liu Y, Lai YC, Hill EV, et al. Phosphatidylinositol 3-phosphate 5-kinase (PIKfyve) is an AMPK target participating in contraction-stimulated glucose uptake in skeletal muscle. Biochem J. 2013 Oct 15;455(2):195-206. PMID: 23905686.

Martin S, Harper CB, May LM, et al. Inhibition of PIKfyve by YM-201636 dysregulates autophagy and leads to apoptosis-independent neuronal cell death. PLoS One. 2013;8(3):e60152. PMID: 23544129.

Jefferies HB, Cooke FT, Jat P, et al. A selective PIKfyve inhibitor blocks PtdIns(3,5)P(2) production and disrupts endomembrane transport and retroviral budding. EMBO Rep. 2008 Feb;9(2):164-70. PMID: 18188180.

Custom Order

  • Size of single unit expressed as number (e.g. '500' in the case of 500 mg)
  • Total quantity of unit size desired (e.g. '10' in the case of 10 x 500 mg). If only one unit is desired, you may leave this blank.
  • This field is for validation purposes and should be left unchanged.

Related Products

  • S8344

    R,S-(±)-Sulpiride

    GHB agonist, D2/3 antagonist.
    ≥98%
  • U6856

    Urocortin II, human

    Endogenous peptide, involved in stress signaling; ...
    ≥95%
  • A1332

    Adipokinetic Hormone II from Locusta migratoria

    Neuropeptide found in Locusta migratoria.
    ≥98%
  • C1619

    CEF3

    Peptide, vSrc-induced cytokine.
    ≥95%
  • C1844

    Celastrol

    Triterpene isolated Trypterigium wilfordii; HSP90 ...
    ≥98%
  • I7356

    Isopropyl Thiogalactoside

    Galactose analog, allolactose mimic, induces activ...
    ≥98%
  • T3094

    Thymopentin Acetate

    Peptide fragment of thymopoietin, immunostimulant.
    ≥95%
  • O4658

    Olopatadine Hydrochloride

    Mast cell stabilizer; histamine H1/2/3 antagonist.
    ≥99%
  • N3350

    Nimorazole

    Nitroimidazole; hypoxic modifier and radiosensitiz...
    ≥98%
  • C1624

    Cefuroxime Sodium

    β-lactam; penicillin binding protein inhibitor.
    ≥98%
  • T2935

    Thiamphenicol

    Chloramphenicol derivative; protein translation in...
    ≥98%
  • H9718

    2-Hydroxyflutamide

    Non-steroid; AR antagonist.
    ≥98%
  • T7156

    Tropisetron Hydrochloride

    α7 nAChR partial agonist, 5-HT3 antagonist.
    ≥98%
  • S7601

    Statil

    Aldose reductase inhibitor.
    ≥98%
  • V5870

    Vortioxetine

    5-HT1A agonist, 5-HT1B partial agonist, 5-HT3A/7 a...
    ≥98%
  • A7656

    Atomoxetine Hydrochloride

    NET and SERT inhibitor, NMDA antagonist.
    ≥99%
  • P0013

    P7C3

    Aminopropyl carbazole, neuroprotective.
    ≥98%
  • M8007

    Mubritinib, Free Base

    EGFR2 inhibitor.
    ≥98%
  • D3448

    Dimethyl Fumarate

    Fumaric acid methyl ester; nAChR agonist, indirect...
    ≥98%
  • U6802

    Urapidil Hydrochloride

    5-HT1A agonist, α1-adrenergic antagonist.
    ≥98%

Footer

  • Contact Us
  • About Us
  • Site Map
  • Terms and Conditions
LKT Laboratories, Inc.
545 Phalen Blvd.
St. Paul MN, 55130

Ph: (888)-558-5227
Fax: (888)-558-7329

©2025 LKT Laboratories, All Rights Reserved - Products for research use only