• 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
Evodiamine

Evodiamine

Product ID E8657
Cas No. 518-17-2
Purity ≥98%
Product Unit SizeCostQuantityStock
100 mg $97.20 In stock
250 mg $194.60 In stock
1 g $544.50 In stock
Bulk Quote

Quicklinks

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

Description

Evodiamine is an indole alkaloid originally found in Evodia rutaecarpa. This compound exhibits anticancer, anti-diabetic, antiviral, anti-angiogenic, and gastrointestinal motility modulating activities. In bladder cancer cells, evodiamine decreases levels of Mcl-1, inhibits signaling of mTOR, and enhances TRAIL-induced apoptosis. Evodiamine directly inhibits topoisomerases I and II (topoI, topoII), inducing G2/M phase cell cycle arrest in leukemia cells. In other in vitro models, evodiamine decreases VEGF release and tube formation. In diabetic/obese animal models, evodiamine decreases mTOR signaling and increases phosphorylation of AMPK, improving glucose tolerance. Additionally, this compound inhibits viral replication of Influenza A and suppresses gastric emptying and transit.

Product Info

Cas No.

518-17-2

Purity

≥98%

Formula

C19H17N3O

Formula Wt.

303.36

IUPAC Name

(1S)-21-methyl-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15,17,19-heptaen-14-one

Melting Point

265-278°C

Appearance

Light Yellow Fine Powder

Shipping and Storage

Store Temp

Ambient

Ship Temp

Ambient

Downloads

MSDS

E8657 MSDS PDF

Info Sheet

E8657 Info Sheet PDF

References

Zhang T, Qu S, Shi Q, et al. Evodiamine Induces Apoptosis and Enhances TRAIL-Induced Apoptosis in Human Bladder Cancer Cells through mTOR/S6K1-Mediated Downregulation of Mcl-1. Int J Mol Sci. 2014 Feb 21;15(2):3154-71. PMID: 24566141.

Wang T, Kusudo T, Takeuchi T, et al. Evodiamine inhibits insulin-stimulated mTOR-S6K activation and IRS1 serine phosphorylation in adipocytes and improves glucose tolerance in obese/diabetic mice. PLoS One. 2013 Dec 31;8(12):e83264. PMID: 24391749.

Dai JP, Li WZ, Zhao XF, et al. A drug screening method based on the autophagy pathway and studies of the mechanism of evodiamine against influenza A virus. PLoS One. 2012;7(8):e42706. PMID: 22900043.

Pan X, Hartley JM, Hartley JA, et al. Evodiamine, a dual catalytic inhibitor of type I and II topoisomerases, exhibits enhanced inhibition against camptothecin resistant cells. Phytomedicine. 2012 May 15;19(7):618-24. PMID: 22402246.

Shyu KG, Lin S, Lee CC, et al. Evodiamine inhibits in vitro angiogenesis: Implication for antitumorgenicity. Life Sci. 2006 Apr 4;78(19):2234-43. PMID: 16280136.

Wu CL, Hung CR, Chang FY, et al. Effects of evodiamine on gastrointestinal motility in male rats. Eur J Pharmacol. 2002 Dec 20;457(2-3):169-76. PMID: 12464363.

Sung B, Prasad S, Ravindran J, et al. Capsazepine, a TRPV1 antagonist, sensitizes colorectal cancer cells to apoptosis by TRAIL through ROS-JNK-CHOP-mediated upregulation of death receptors. Free Radic Biol Med. 2012 Nov 15;53(10):1977-1987. PMID: 22922338.

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

  • M1977

    Metronidazole

    Nitroimidazole; DNA synthesis inhibitor.

    ≥98%
  • G4479

    Glucagon (19-29), human

    Endogenous peptide hormone, glugagon fragment; ...

    ≥95%
  • A985130

    AZD-7762

    CHK1 inhibitor.

    ≥98%
  • D1720

    Deferiprone

    Iron chelator.

    ≥99%
  • T2833

    1-Thio-β-D-glucose Tetraacetate

    Imaging agent; Maillard reaction inhibitor.

    ≥98%
  • I5440

    INK128

    mTOR inhibitor.

    ≥99%
  • D324094

    Diclofenac Related Compound A

    Impurity of diclofenac

    ≥98%
  • A9602

    Azacitidine

    Nucleoside (cytidine) analog; DNMT inhibitor, p...

    ≥98%
  • R1877

    all-trans-Retinol, ≥98 %

    Diterpene vitamin A; RAR/RXR agonist.

    ≥98%
  • G1210

    GDC-0623

    MEK inhibitor.

    ≥98%
  • C1635

    Ceftazidime Hydrate

    β-lactam cephalosporin; penicillin binding pro...

    ≥97%
  • S0245

    Salmeterol

    β2-adrenergic agonist.

    ≥98%
  • T0142

    TAK-733

    MEK inhibitor.

    ≥98%
  • T0298

    Tazobactam

    β-lactamase inhibitor.

    ≥98%
  • E9418

    Exendin 3 (9-39)

    Peptide, GLP-1 analog found in Heloderma; GLP-1...

    ≥95%
  • E6781

    (±)-Equol

    Isoflavone, phytoestrogen found in soy; ER agon...

    ≥98%
  • P2994

    Physalaemin

    Amphibian tachykinin neuropeptide.

    ≥95%
  • T9945

    Tylosin Tartrate

    Macrolide; peptidyl transferase inhibitor, prot...

    ≥90%
  • P0144

    Paliperidone

    D2 and 5-HT2A antagonist.

    ≥97%
  • G4798

    Glycitein

    Aglycone isoflavone found in soy and red clover...

    ≥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