• 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
Microcystin-LR

Microcystin-LR

Product ID M3406
Cas No. 101043-37-2
Purity ≥95%
Product Unit SizeCostQuantityStock
100 µg $183.00 Please Inquire
1 mg $1,045.00 Please Inquire
Bulk Quote

Quicklinks

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

Description

Microcystin LR is a cyclic heptapeptide initially produced by species of cyanobacteria Microcystis. Microcystin LR exhibits cytotoxic, pro-oxidative, and carcinogenic properties. Microcystin LR is particularly toxic to the liver, increasing cytochrome c release and expression of Bax and caspases 3, 8, and 9; microcystin LR also decreases expression of Bcl-2. In testicular cells, this toxin increases expression of c-KIT and induces apoptosis, causing a decrease in tubular diameter and testes weight. This compound also induces cytoskeletal reorganization, increasing phosphorylation of VASP and tau and also increasing dissociation of tau from the cytoskeleton. In vitro, Microcystin LR inhibits protein phosphatases 1 (PP1) and 2A (PP2A) and induces oxidative damage by increasing levels of ROS and malondialdehyde and decreasing levels of glutathione and glutathione peroxidase. Microcystin LR also produces cognitive deficit in vivo, potentially through activation of glycogen synthase kinase-3β (GSK-3β). This compound also activates Nrf2 in cancer cells.

Product Info

Cas No.

101043-37-2

Purity

≥95%

Formula

C49H74N10O12

Formula Wt.

995.17

IUPAC Name

(5R,8S,11R,12S,15S,18S,19S,22R)-15-[3-(diaminomethylideneamino)propyl]-18-[(1E,3E,5S,6S)-6-methoxy-3,5-dimethyl-7-phenylhepta-1,3-dienyl]-1,5,12,19-tetramethyl-2-methylidene-8-(2-methylpropyl)-3,6,9,13,16,20,25-heptaoxo-1,4,7,10,14,17,21-heptazacyclopentacosane-11,22-dicarboxylic acid

Synonym

Cyanoginosin-LR, MC-LR

Solubility

Soluble in ethanol, DMSO, methanol (10 mg/mL).

Appearance

Clear film

Shipping and Storage

Store Temp

-20°C

Ship Temp

Blue Ice

Downloads

MSDS

M3406 MSDS PDF

Info Sheet

M3406 Info Sheet PDF

References

Zhou Y, Chen Y, Yuan M, et al. In vivo study on the effects of microcystin-LR on the apoptosis, proliferation and differentiation of rat testicular spermatogenic cells of male rats injected i.p. with toxins. J Toxicol Sci. 2013;38(5):661-70. PMID: 24025782.

Sun Y, Liu JH, Huang P, et al. Alterations of tau and VASP during microcystin-LR-induced cytoskeletal reorganization in a human liver cell line. Environ Toxicol. 2013 Aug 9. doi:. [Epub ahead of print]. PMID: 23929704.

Zhang H, Cai C, Fang W, et al. Oxidative damage and apoptosis induced by microcystin-LR in the liver of Rana nigromaculata in vivo. Aquat Toxicol. 2013 Sep 15;140-141:11-8. PMID: 23747548.

Wang J, Lin F, Cai F, et al. Microcystin-LR inhibited hippocampal long-term potential via regulation of the glycogen synthase kinase-3β pathway. Chemosphere. 2013 Sep;93(2):223-9. PMID: 23701903.

Liang J, Li T, Zhang YL, et al. Effect of microcystin-LR on protein phosphatase 2A and its function in human amniotic epithelial cells. J Zhejiang Univ Sci B. 2011 Dec;12(12):951-60. PMID: 22135143.

Gan N, Sun X, Song L. Activation of Nrf2 by microcystin-LR provides advantages for liver cancer cell growth. Chem Res Toxicol. 2010 Sep 20;23(9):1477-84. PMID: 20722399.

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

  • M184770

    4-O-Methylhonokiol

    Found in Magnolia officinalis.

    ≥98%
  • Z161023

    β-Zearalanol

    Mycotoxin that has structural similarity to est...

    ≥98%
  • T2932

    Thiamphenicol Glycinate Hydrochloride

    Chloramphenicol derivative; protein translation...

    ≥98%
  • P0344

    Palbociclib Isethionate

    CDK4/6 inhibitor.

    ≥98%
  • A5059

    Amoxapine

    5-HT2/3/6/7, D2/3/4, histamine H1, α1-adrenerg...

    ≥98%
  • A5284

    [Val5]-Angiotensin II, human

    Peptide, derivative of AT II, involved in vasoc...

    ≥95%
  • S9754

    Syntide 2

    Synthetic peptide, CDPK, PKC, CaMKII substrate....

    ≥95%
  • K0053

    Kanamycin A Monosulfate

    Aminoglycoside; protein translation inhibitor, ...

    ≥98%
  • M1779

    Methyldopa Sesquihydrate

    DOPA decarboxylase inhibitor, indirect α2-adre...

    ≥98%
  • T5604

    Tobramycin, Free Base

    Aminoglycoside; protein translation inhibitor.<...

    ≥98%
  • B0396

    BAY80-6946

    p110α PI3K inhibitor.

    ≥98%
  • A0902

    N-Acetyl-S-(N′-phenylhexylthiocarbamoyl)-L-cysteine

    Cysteine-ITC conjugate, antioxidant; HDAC inhib...

    ≥98%
  • G2869

    Ghrelin, rat

    Endogenous peptide hormone, involved in feeding...

    ≥95%
  • A6933

    Aristolochic Acid B

    Found in Aristolochia and Radix; potential PLA2...

    ≥95%
  • B8070

    2-tert-Butyl-4-Hydroxyanisole

    BHA derivative, antioxidative food and cosmetic...

    ≥99% single isomer
  • L1340

    LDK378

    ALK and IGF-1R inhibitor.

    ≥99%
  • T3032

    Thienyldecyl Isothiocyanate

    Thienylbutyl ITC analog.

    ≥95%
  • G0145

    Gallic Acid

    Phenol found in various plant sources, used to ...

    ≥98%
  • I0417

    R-(−)-Iberin

    Sulforaphane homolog, ITC found in cruciferous ...

    ≥98%
  • F6803

    FRAX486

    PAK inhibitor.Smo 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

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