• 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
Chaetocin

Chaetocin

Product ID C281006
Cas No. 28097-03-2
Purity ≥98%
Product Unit SizeCostQuantityStock
1 mg $245.00 In stock
5 mg $900.00 In stock
Bulk Quote

Quicklinks

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

Description

Chaetocin is naturally produced by Chaetomium species fungi. In human melanoma cells, treatment with chaetocin suppressed proliferation, induced apoptosis, and increased the level of reactive oxygen species. In Epstein-Barr virus cells, chaetocin apparently up-regulated lytic transcription and DNA replication via the ROS pathways. In a rat model of chronic heart failure, chaetocin treatment prolonged survival and restored mitochondrial dysfunction. Using NCI-60 screening found chaetocin to inhibit proliferation in all tested solid tumor cells even more so than multiple myeloma cells. Chaetocin was also observed to cause a 25-fold induction of latent HIV-1 expression which may be an effective way to purge cells of latent HIV-1.

Product Info

Cas No.

28097-03-2

Purity

≥98%

Formula

C30H28N6O6S4

Formula Wt.

696.83

Chemical Name

Chaetocin

IUPAC Name

(1~{S},3~{R},11~{R},14~{S})-14-(hydroxymethyl)-3-[(1~{S},3~{R},11~{R},14~{S})-14-(hydroxymethyl)-18-methyl-13,17-dioxo-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0^{1,12}.0^{3,11}.0^{4,9}]octadeca-4,6,8-trien-3-yl]-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0^{1,12}.0^{3,11}.0^{4,9}]octadeca-4,6,8-triene-13,17-dione

Shipping and Storage

Store Temp

-20°C

Ship Temp

Ambient

Downloads

MSDS

C281006 MSDS PDF

Info Sheet

C281006 Info Sheet PDF

References

Han X, Han Y, Zheng Y, et al. Chaetocin induces apoptosis in human melanoma cells through the generation of reactive oxygen species and the intrinsic mitochondrial pathway, and exerts its anti-tumor activity in vivo. PLoS One. 2017 Apr 18;12(4):e0175950. PMID: 28419143.

Zhang S, Yin J, Zhong J. Chaetocin reactivates the lytic replication of Epstein-Barr virus from latency via reactive oxygen species. Sci China Life Sci. 2017 Jan;60(1):66-71. PMID: 28063010.

Ono T, Kamimura N, Matsuhashi T, et al. The histone 3 lysine 9 methyltransferase inhibitor chaetocin improves prognosis in a rat model of high salt diet-induced heart failure. Sci Rep. 2017 Jan 4;7:39752. PMID: 28051130.

Isham CR, Tibodeau JD, Bossou AR, et al. The anticancer effects of chaetocin are independent of programmed cell death and hypoxia, and are associated with inhibition of endothelial cell proliferation. Br J Cancer. 2012 Jan 17;106(2):314-323. PMID: 22187030.

Bernhard W, Barreto K, Saunders A, et al. The Suv39H1 methyltransferase inhibitor chaetocin causes induction of integrated HIV-1 without producing a T cell response. FEBS Lett. 2011 Nov 16;585(22):3549-3554. PMID: 22020221.

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

  • A4930

    7-Aminoactinomycin D

    Actinomycin derivative used to study apoptosis and...
    ≥97%
  • M1335

    Mdivi-1

    Quinazolinone; mitochondrial division inhibitor.
    ≥98%
  • V0269

    Vardenafil Dihydrochloride

    PDE5 inhibitor.
    ≥98%
  • N8604

    NVP-BGT226

    PI3K and mTOR inhibitor.
    ≥98%
  • E9819

    Ezetimibe

    NPC1L1 inhibitor.
    ≥99%
  • I5315

    Indomethacin

    NSAID; COX-1/2 inhibitor.
    ≥98%
  • T5846

    Tolfenamic Acid

    NSAID; COX-1/2 inhibitor.
    ≥98%
  • P7034

    Prion Peptide (106-126), human

    Synthetic peptide fragment, prion protein analog; ...
    ≥95%
  • A464768

    Altertoxin 1

    Mycotoxin contaminant in food and feed.
    ≥97%
  • L0254

    Lansoprazole

    H+/K+ ATPase inhibitor.
    ≥98%
  • F5874

    Fosfomycin Calcium

    MurA and isopentenyl mevalonate kinase inhibitor.
    ≥97%
  • T0081

    Taurine

    Endogenous sulfonic acid involved in Ca2+ signalin...
    ≥98%
  • AS107

    Caffeic Acid Esters Standards Kit

    Caffeic Acid Esters Standards Kit Contents: -Colum...
  • R5773

    Rosiglitazone

    Thiazolidinedione; PPARγ agonist.
    ≥98%
  • A0961

    Adrenocorticotropic Hormone (1-39), rat

    Endogenous peptide hormone, involved in stress sig...
    ≥95%
  • A9814

    AZD-4547

    FGFR inhibitor.
    ≥98%
  • A1330

    Adipokinetic Hormone

    Neuropeptide hormone found in insects, involved in...
    ≥95%
  • V2792

    VGX-1027

    TLR4 inhibitor.
    ≥98%
  • O4400

    Olanzapine

    AMPK activator, D1-4, 5-HT1A/2/3/6/7, M1-5 mAChR, ...
    ≥98%
  • G3253

    8-Gingerol

    Phenol found in Zingiber; 5-HT3 antagonist.
    ≥99%

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

©2026 LKT Laboratories, All Rights Reserved - Products for research use only