• 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
Gabexate Mesylate

Gabexate Mesylate

Product ID G0104
Cas No. 56974-61-9
Purity ≥99%
Product Unit SizeCostQuantityStock
10 mg $155.80 In stock
100 mg $778.60 In stock
250 mg $1,557.20 In stock
Bulk Quote

Quicklinks

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

Description

Gabexate displays anticancer chemotherapeutic, anti-angiogenic, anti-inflammatory, and antiviral activities. In vitro, gabexate inhibits the activation of NF-κB, ERK1/2, and Akt, downregulates the production of matrix metalloproteinases 2 and 9, VEGF, and IL-8, and increases expression of protein and phosphatase and tensin homolog (PTEN). Gabexate acts as a proteasome inhibitor, inhibiting activity of tumor-associated trypsinogen and urokinase-type plasminogen activator and decreasing the invasiveness of pancreatic cancer cells. Additionally, gabexate inhibits production of TNF-α, preventing activation of MAPK signaling cascades in vitro. This compound also exhibits antiviral activity against the influenza virus, inhibiting cleavage of hemagglutinin.

Product Info

Cas No.

56974-61-9

Purity

≥99%

Formula

C16H24N3O4 • CH3O3S

Formula Wt.

417.48

Chemical Name

ethyl 4-[6-(diaminomethylideneamino)hexanoyloxy]benzoate;methanesulfonic acid

IUPAC Name

ethyl 4-[6-(diaminomethylideneamino)hexanoyloxy]benzoate;methanesulfonic acid

Synonym

4-[[6-[ (aminoiminomethyl) amino]-1-oxohexyl]oxyl]benzoic acid ethyl ester mesylate salt

Melting Point

90-93℃

Appearance

White to off white powder

Shipping and Storage

Store Temp

Ambient

Ship Temp

Ambient

Downloads

MSDS

G0104 MSDS PDF

Info Sheet

G0104 Info Sheet PDF

References

Brandi G, Tavolari S, Guarnieri T, et al. Antiprotease strategy in pancreatic cancer treatment: emergence from a preclinical study. Pancreas. 2014 Jan;43(1):53-63. PMID: 24201777.

Hsieh HP, Hsu JT. Strategies of development of antiviral agents directed against influenza virus replication. Curr Pharm Des. 2007;13(34):3531-42. PMID: 18220789.

Uchima Y, Sawada T, Nishihara T, et al. Inhibition and mechanism of action of a protease inhibitor in human pancreatic cancer cells. Pancreas. 2004 Aug;29(2):123-31. PMID: 15257104.

Yuksel M, Okajima K, Uchiba M, et al. Gabexate mesilate, a synthetic protease inhibitor, inhibits lipopolysaccharide-induced tumor necrosis factor-alpha production by inhibiting activation of both nuclear factor-kappaB and activator protein-1 in human monocytes. J Pharmacol Exp Ther. 2003 Apr;305(1):298-305. PMID: 12649382.

Aosasa S, Ono S, Mochizuki H, et al. Mechanism of the inhibitory effect of protease inhibitor on tumor necrosis factor alpha production of monocytes. Shock. 2001 Feb;15(2):101-5. PMID: 11220636.

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

  • B3374

    Bisacodyl

    Diphenylmethane derivative, stimulates colonic ...

    ≥98%
  • N1610

    Necrostatin-1

    RIP1 inhibitor.

    ≥99%
  • H965143

    Hydrolyzed Fumonisin B2

    Mycotoxin produced by Fusarium fungi that infec...

    ≥97% by ELSD
  • S771339

    STING Agonist-12

    STING activator

    ≥99%
  • C294458

    Chlorzoxazone

    Centrally acting muscle relaxant.

    ≥99%
  • L1780

    Levocetirizine Dihydrochloride

    L-isomer of cetirizine; histamine H1 antagonist...

    ≥98%
  • P2859

    Phosphate Acceptor Peptide

    PKC and S6 kinase substrate.

    ≥95%
  • L5767

    Loratadine

    Histamine H1 antagonist, FIASMA.

    ≥98%
  • M0040

    M40

    Peptide; galanin antagonist.

    ≥95%
  • T3461

    Tiplaxtinin

    PAI-1 inhibitor.

    ≥98%
  • N3476

    Nitisinone

    Nitrobenzene; HPPD inhibitor.

    ≥99%
  • C1844

    Celastrol

    Triterpene isolated Trypterigium wilfordii; HSP...

    ≥98%
  • T5604

    Tobramycin, Free Base

    Aminoglycoside; protein translation inhibitor.<...

    ≥98%
  • B0026

    Bafilomycin B1

    Macrolide; vacuolar H+-ATPase inhibitor.

    ≥97%
  • D5868

    Doramapimod

    JNK, ALK, p38 MAPK inhibitor.

    ≥99%
  • C2802

    CH5132799

    p110α PI3K inhibitor.

    ≥98%
  • A1592

    ADX-47273

    mGluR5 positive modulator.

    ≥98%
  • R3449

    Rimonabant Hydrochloride

    CB1 inverse agonist.

    ≥98%
  • B8676

    BVT-2733

    11β-HSD1 inhibitor.

    ≥98%
  • F5968

    Foretinib

    ROS1, MET, Ron, Axl, TIE-2, VEGFR2 inhibitor.

    ≥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