• 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
Pifithrin-α Hydrobromide

Pifithrin-α Hydrobromide

Product ID P327211
Cas No. 63208-82-2
Purity ≥98%
Product Unit SizeCostQuantityStock
5 mg $75.10 In stock
10 mg $120.20 In stock
25 mg $285.60 In stock
100 mg $788.90 In stock
Bulk Quote

Quicklinks

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

Description

Pifithrin-alpha is a small molecule inhibitor of p53 shown to prevent neuronal death induced by DNA damage. Pifithrin-alpha has also been found to interfere in heat shock and glucocorticoid receptor signaling pathways. Both in vivo and in vitro pifithrin-alpha inhibited firefly luciferase activity.

Product Info

Cas No.

63208-82-2

Purity

≥98%

Formula

C16H18N2OS • HBr

Formula Wt.

367.31

Chemical Name

2-(2-imino-4,5,6,7-tetrahydro-1,3-benzothiazol-3-yl)-1-(4-methylphenyl)ethanone;hydrobromide

IUPAC Name

2-(2-Imino-4,5,6,7-tetrahydro-1,3-benzothiazol-3(2H)-yl)-1-(4-methylphenyl)ethanone hydrobromide (1:1)

Synonym

Pifithrin-alpha.HBr, PFT-alpha

Solubility

Soluble in DMSO to 100 mM

Shipping and Storage

Store Temp

-20°C

Ship Temp

Ambient

Downloads

MSDS

P327211 MSDS PDF

Info Sheet

P327211 Info Sheet PDF

References

Komarova EA, Nenanov N, Komarov PG, et al. p53 inhibitor pifithrin alpha can suppress heat shock and glucocorticoid signaling pathways. J Biol Chem. 2003 May 2;278(18):15465-15468. PMID: 12637507.

Rocha S, Campbell KJ, Roche KC, et al. The p53-inhibitor pifithrin-alpha inhibits firefly luciferase activity in vivo and in vitro. BMC Mol Biol. 2003 Sep 11;4:9. PMID: 12967348.

Kanno S, Kurachi K, Tomizawa A, et al. Pifithrin-alpha has a p53-independent cytoprotective effect on docosahexaenoic acid-induced cytotoxicity in human hepatocellular carcinoma HepG2 cells. Toxicl Lett. 2015 Jan 22, 232(2):393-402. PMID: 25448278.

Murphy PJ, Galigniana MD, Morishima Y, et al. Pifithrin-alpha inhibits p53 signaling after interaction of the tumor suppressor protein with hsp90 and its nuclear translocation. J Biol Chem. 2004 Jul 16;279(29):30195-30201. PMID: 15145929.

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

  • P3469

    Pirfenidone

    Collagen synthesis inhibitor.

    ≥98%
  • B1879

    Betamethasone Valerate

    Synthetic steroid hormone; glucocorticoid agoni...

    ≥98%
  • L1981

    Leucokinin VIII

    Peptide found in insects.

    ≥95%
  • L582694

    Lorlatinib

    Third generation macrocyclic ALK inhibitor.

    ≥98%
  • A5284

    [Val5]-Angiotensin II, human

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

    ≥95%
  • K0117

    Kaempferol

    Flavonol found in various plant sources.

    ≥98%
  • U6857

    Urodilatin CCC

    ANP fragment, natriuretic peptide; Na+/K+ ATPas...

    ≥98%
  • T0105

    Taxol C

    Taxane synthesis intermediate.

    ≥95%
  • D5709

    Docetaxel

    Semi-synthetic analog of taxol; microtubule depoly...
    ≥98%
  • N3322

    Niflumic Acid

    NSAID; NMDA inverse agonist, T-type Ca2+ and Cl...

    ≥98%
  • E6259

    Epoxiconazole

    Triazole; 14-α demethylase inhibitor, potentia...

    ≥95%
  • C000171

    C-171

    STING inhibitor

    ≥98%
  • P2012

    PF-04217903

    Triazolopyrazine; c-MET inhibitor.

    ≥98%
  • E4668

    ELR-510444

    Microtubule polymerization inhibitor.

    ≥98%
  • E6376

    Eptifibatide

    Glycoprotein IIb/IIIa inhibitor.

    ≥98%
  • T2404

    TG101348

    JAK2 inhibitor.

    ≥98%
  • K0144

    Kallikrein Inhibitor

    Peptide; serine protease inhibitor.  
    ≥95%
  • B1753

    Benfotiamine

    Thiamine/vitamin B derivative, antioxidant.

    ≥98%
  • I761004

    Itaconic Acid

    Polymer precursor

    ≥99%
  • S6800

    SR1001

    RORα/γ inverse agonist.

    ≥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

©2025 LKT Laboratories, All Rights Reserved - Products for research use only