• 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
Finasteride

Finasteride

Product ID F3354
Cas No. 98319-26-7
Purity ≥98%
Product Unit SizeCostQuantityStock
100 mg $104.10 In stock
500 mg $388.50 In stock
Bulk Quote

Quicklinks

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

Description

Finasteride is an inhibitor of steroid 5-α-reductase that decreases metabolism of testosterone, decreasing cell proliferation and fluid production in the prostate; it is clinically used to treat benign prostatic hyperplasia (BPH) and male pattern baldness. Finasteride also exhibits antifungal and anticancer chemotherapeutic activities. Finasteride inhibits growth of Candida. Additionally, finasteride suppresses regrowth of regressed prostate tumors and inhibits cell proliferation in vivo and in vitro in short term application models.

Product Info

Cas No.

98319-26-7

Purity

≥98%

Formula

C23H36N2O2

Formula Wt.

372.54

Chemical Name

(5α,17β)-N-(1,1-Dimethylethyl)-3-oxo-4-azaandrost- 1-ene-17-carboxamide

IUPAC Name

(1S,3aS,3bS,5aR,9aR,9bS,11aS)-N-tert-butyl-9a,11a-dimethyl-7-oxo-1,2,3, 3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide

Synonym

Finastid, Propecia, Proscar, Prostide

Melting Point

252-254°C °r 257°C

Solubility

Soluble in chloroform. DMSO, ethanol and methanol. Slighly soluble in water.

Appearance

White/off-white Crystal Powder

Shipping and Storage

Store Temp

Ambient

Ship Temp

Ambient

Downloads

MSDS

F3354 MSDS PDF

Info Sheet

F3354 Info Sheet PDF

References

Chavez-Dozal AA, Lown L, Jahng M, et al. An in vitro analysis of finasteride activity against Candida albicans urinary biofilm formation and filamentation. Antimicrob Agents Chemother. 2014 Jul 21. [Epub ahead of print]. PMID: 25049253.

Masoodi KZ, Ramos Garcia R, Pascal LE, et al. 5α-reductase inhibition suppresses testosterone-induced initial regrowth of regressed xenograft prostate tumors in animal models. Endocrinology. 2013 Jul;154(7):2296-307. PMID: 23671262.

Zager MG, Barton HA. A multiscale, mechanism-driven, dynamic model for the effects of 5α-reductase inhibition on prostate maintenance. PLoS One. 2012;7(9):e44359. PMID: 22970204.

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

  • P7608

    PTC124

    Read-through agent and nonsense mutation targeter.
    ≥98%
  • B6916

    Brevetoxin 1

    Brevetoxins are lipid-soluble polyether neurotoxin...
    ≥95%
  • A6002

    Apamin

    Peptide, bee venom toxin; SK2/3/4 K+ channel block...
    ≥95%
  • E5212

    Endonuclease Antigenic Site

    HIV-1 endonuclease CTL binding pocket fragment.
    ≥98%
  • C6982

    Crustacean Cardioactive Peptide

    Neuropeptide hormone found in arthropods.
    ≥95%
  • O9396

    Oxytetracycline

    Tetracycline; protein translation inhibitor.
    ≥96%
  • E9819

    Ezetimibe

    NPC1L1 inhibitor.
    ≥99%
  • C2803

    Chartreusin

    Binds DNA; RNA synthesis inhibitor.
    ≥98%
  • V1745

    Veliparib

    PARP inhibitor.
    ≥99%
  • Z4552

    ZLN005

    PPARγ coactivator-1α expression stimulator.
    ≥98%
  • V5725

    Voglibose

    α-glucosidase inhibitor, potential GLP-1 agonist,...
    ≥98%
  • D0262

    Dapiprazole Hydrochloride

    α1-Adrenergic antagonist.
    ≥98%
  • T3040

    Thienylpentyl Isothiocyanate

    Thienylbutyl ITC analog.
    ≥98%
  • C0156

    9-Nitro-20S-camptothecin

    Camptothecin derivative; topoisomerase I inhibitor...
    ≥98%
  • N3577

    Nitidine Chloride

    Benzophenanthridine alkaloid; topoisomerase I inhi...
    ≥98%
  • C1879

    Cetrorelix Acetate

    Peptide, GnRH analog;GnRH agonist.
    ≥95%
  • D1773

    Deshydroxy LY-411575

    γ-Secretase inhibitor.
    ≥98%
  • D0010

    3H-1,2-Dithiole-3-thione

    Induces activation of Nrf2; inhibits apoptosis in ...
    ≥98%
  • I0416

    Iberin

    Isothiocyanate found in cruciferous vegetables, ho...
    ≥97%
  • C5773

    Cortistatin-14

    Endogenous neuropeptide, somatostatin analog; soma...
    ≥95%

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