• 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
YC-1

YC-1

Product ID Y0800
Cas No. 170632-47-0
Purity ≥98%
Product Unit SizeCostQuantityStock
1 mg $47.30 Please Inquire
5 mg $153.70 Please Inquire
25 mg $614.70 Please Inquire
Bulk Quote

Quicklinks

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

Description

YC-1 is a guanylyl cyclase activator and HIF-1α inhibitor. YC-1 displays anti-fibrotic, anticancer chemotherapeutic, anti-atherosclerotic, and neuroprotective activities. In vitro, YC-1 decreases secretion of sENG and sFlt-1, reversing endothelial dysfunction. In hepatic stellate cells, this compound decreases cell viability and increases apoptosis, potentially through suppressing expression of αSMA. In canine lymphoma cells, YC-1 inhibits cell proliferation; in similar animal models, it induces tumor regression. In other animal models, YC-1 decreases ox-LDL-induced cholesterol accumulation. Additionally, this compound suppresses neuronal death induced by amyloid-β (Aβ) peptides.

Product Info

Cas No.

170632-47-0

Purity

≥98%

Formula

C19H16N2O2

Formula Wt.

304.35

Chemical Name

[5-(1-Benzyl-1H-indazol-3-yl)-2-furyl]methanol

IUPAC Name

[5-(1-Benzyl-1H-indazol-3-yl)-2-furyl]methanol

Synonym

3-(5'-Hydroxymethyl-2'-furyl)-1-benzylindazole

Solubility

Soluble in DMSO, methanol or dichloromethane.

Appearance

White to pale yellow powder.

Shipping and Storage

Store Temp

-20°C

Ship Temp

Ambient

Downloads

MSDS

Y0800 MSDS PDF

Info Sheet

Y0800 Info Sheet PDF

References

Brownfoot FC, Tong S, Hannan NJ, et al. YC-1 reduces placental sFlt-1 and soluble endoglin production and decreases endothelial dysfunction: A possible therapeutic for preeclampsia. Mol Cell Endocrinol. 2015 Sep 15;413:202-8. PMID: 26159901.

Xiao J, Jin C, Liu Z, et al. The design, synthesis, and biological evaluation of novel YC-1 derivatives as potent anti-hepatic fibrosis agents. Org Biomol Chem. 2015 Jul 14;13(26):7257-64. PMID: 26055070.

Kambayashi S, Igase M, Kobayashi K, et al. Hypoxia inducible factor 1α expression and effects of its inhibitors in canine lymphoma. J Vet Med Sci. 2015 Jun 6. [Epub ahead of print]. PMID: 26050843.

Tsou CY, Chen CY, Zhao JF, et al. Activation of soluble guanylyl cyclase prevents foam cell formation and atherosclerosis. Acta Physiol (Oxf). 2014 Apr;210(4):799-810. PMID: 24299003.

Purohit R, Fritz BG, The J, et al. YC-1 binding to the β subunit of soluble guanylyl cyclase overcomes allosteric inhibition by the α subunit. Biochemistry. 2014 Jan 14;53(1):101-14. PMID: 24328155.

Tsai YC, Lee YM, Lam KK, et al. The role of heat shock protein 70 in the protective effect of YC-1 on β-amyloid-induced toxicity in differentiated PC12 cells. PLoS One. 2013 Jul 26;8(7):e69320. PMID: 23922702.

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

  • P3462

    Piperacillin

    β-lactam; penicillin binding protein inhibitor...

    ≥95%
  • M7200

    MS436

    BRD4 inhibitor.

    ≥99%
  • L4796

    LY-294002

    PI3K inhibitor.

    ≥99%
  • I5752

    Ionomycin, Free Acid

    Polyether Ca2+ ionophore.

    ≥98%, TLC, HPLC
  • T5608

    α-Tocotrienol

    Antioxidant, vitamin E derivative found in vege...

    ≥98%
  • E9317

    Exemestane

    Aromatase inhibitor.

    ≥97%
  • A488246

    AMG-232

    MDM2-p53 inhibitor

    ≥99%
  • L1616

    LEE-011

    CDK4/6 inhibitor.

    ≥98%
  • G124080

    GDC-0994

    ERK1/2 inhibitor.

    ≥98%
  • C0378

    Catharanthine Tartrate

    Alkaloid found in Catharanthus, precursor in sy...

    ≥97%
  • I611325

    IPI-549

    Selective inhibitor of the γ isoform of PI3K (...

    ≥98%
  • D5746

    Dolasetron

    5-HT3 antagonist.

    ≥98%
  • P2502

    Phenethyl Glucosinolate Potassium

    Found in cruciferous vegetables.

    ≥97%
  • C9615

    Cyclosporin B

    Cyclic peptide; calcineurin inhibitor.

    ≥95%
  • A5378

    Antimycin A

    Oxidative phosphorylation inhibitor.  
  • P1917

    Phenylethyl 3-methylcaffeate

    Derivative of methyl caffeate, hydroxycinnamic ...

    ≥97%
  • D3329

    7,8-Dihydroxyflavone Hydrate

    TrkB agonist.

    ≥99%
  • A0965

    Adrenocorticotropic Hormone (1-14)

    Endogenous peptide hormone fragment, involved i...

    ≥95%
  • B6959

    Bromosporine

    BRD2/4/9 and CECR2 inhibitor.

    ≥99%
  • Z5653

    Zonisamide

    Sulfonamide; carbonic anhydrase inhibitor, volt...

    ≥96%

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