• 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
NU-2058

NU-2058

Product ID N800000
Cas No. 161058-83-9
Purity ≥98%
Product Unit SizeCostQuantityStock
5 mg $88.60 In stock
25 mg $238.60 In stock
100 mg $715.60 In stock
Bulk Quote

Quicklinks

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

Description

NU-2058 is a guanine-based cyclin-dependent kinase (CDK) inhibitor with selectivity for CDK1/2. In androgen-independent prostate cancer, NU-2058 shows efficacy in bicalutamide-resistant cells. It also inhibits the proliferation of breast cancer cells lines regardless of genetic background or sensitivity to anti-estrogens. NU-2058 and other CDK1/2 inhibitors are a possible therapeutic path for endocrine-resistant breast cancer.

Product Info

Cas No.

161058-83-9

Purity

≥98%

Formula

C12H17N5O

Formula Wt.

247.30

IUPAC Name

6-(Cyclohexylmethoxy)-3H-purin-2-amine

Synonym

NU2058, O6-Cyclohexylmethylguanine

Shipping and Storage

Store Temp

4°C

Ship Temp

Ambient

Downloads

MSDS

N800000 MSDS PDF

Info Sheet

N800000 Info Sheet PDF

References

Rigas, A., Robson, C., et al. Therapeutic potential of CDK inhibitor NU2058 in androgen-independent prostate cancer. Oncogene. 26(55): 7611-7619 (2007). PMID 17599054.

Johnson N., Bentley J., et al. Pre-clinical evaluation of cyclin-dependent kinase 2 and 1 inhibition in anti-estrogen-sensitive and resistant breast cancer cells. Br J Cancer. 102(2):342-350 (2010). PMID: 20010939.

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

  • G8850

    GW-5074

    c-Raf inhibitor.

    ≥98%
  • I0801

    IC261

    Casein kinase 1 inhibitor.

    ≥98%
  • B8112

    Budesonide

    Steroid; glucocorticoid agonist.

    ≥97%
  • Y4802

    YM-201636

    PIKfyve inhibitor.

    ≥98%
  • V3345

    Vildagliptin

    DPP4 inhibitor.

    ≥98%
  • D1694

    Dexamethasone Acetate Monohydrate

    Steroid; glucocorticoid agonist.

    ≥98%
  • G691343

    Griseofulvin

    Fungistatic

    ≥98%
  • P1761

    Pepstatin

    Aspartyl protease inhibitor.

    ≥98%
  • G1658

    Gentamycin Sulfate

    Aminoglycoside; protein translation inhibitor.<...

  • N1986

    Neuropeptide Y, human/rat

    Endogenous peptide neurotransmitter, involved i...

    ≥95%
  • D5612

    2-n-Dodecylfuran

    Furan derivative.

    ≥98%
  • L8008

    D-Luciferin, firefly, Free Acid

    Heterocyclic light-emitting compound, natural l...

    ≥98%
  • W2933

    WHI-P131

    JAK3 and EGFR inhibitor.

    ≥99%
  • C0267

    Carnosol

    Diterpene compound originally found in Rosmarin...

    ≥98%
  • M177521

    Menaquinone-7

    2-methyl-1,4-naphthoquinone derivative

    98%
  • N5770

    Norfloxacin Hydrochloride

    First generation fluoroquinolone antibiotic.

    ≥98%
  • T1025

    D-Seco Paclitaxel

    D-Seco Paclitaxel is an impurity in the product...

    ≥90%
  • D760022

    DT-2216

    BCL-XL specific degrader

    ≥98%
  • A5031

    4-Aminophenylphosphate Disodium

    Alkaline phosphatase substrate used to quantify...

    ≥98%
  • F4783

    Fluvoxamine Maleate

    FIASMA, 5-HT3 and σ1 agonist, SERT inhibitor.<...

    ≥97%

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