• 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
Temsirolimus

Temsirolimus

Product ID T176503
Cas No. 162635-04-3
Purity ≥98%
Product Unit SizeCostQuantityStock
5 mg $100.00 In stock
25 mg $341.00 In stock
100 mg $893.00 In stock
Bulk Quote

Quicklinks

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

Description

Temsirolimus is an analog of rapamycin found to be active against several cancer types. Like rapamycin, temsirolimus is also an mTOR inhibitor. Temsirolimus has shown activity against brain, rhabdomyosarcoma, multiple myeloma, breast, tuberous sclerosis complex, acute lymphoblastic leukemia, pancreatic, prostate, neuroendocrine, renal cell carcinoma, neuroblastoma, and several other cancer types. When treated with temsirolimus, oral squamous cell carcinoma cell’s proliferation and migration were inhibited in vitro and growth of xenografts was suppressed in vivo. Furthermore, in animal models of Parkinson’s disease, treatment with temsirolimus led to increased expression of markers including tyrosine hydroxylase and dopamine transporter and also decreased the upregulation of alpha-synuclein in the substantia nigra after MPTP-induced neurotoxicity. Temsirolimus was found to modulate the autophagic process and the neuroinflammatory pathway in Parkinson’s disease, demonstrating a neuroprotective effect.

Product Info

Cas No.

162635-04-3

Purity

≥98%

Formula

C56H87NO16

Formula Wt.

1030.30

Chemical Name

Temsirolimus

IUPAC Name

[(1~{R},2~{R},4~{S})-4-[(2~{R})-2-[(1~{R},9~{S},12~{S},15~{R},16~{E},18~{R},19~{R},21~{R},23~{S},24~{Z},26~{E},28~{E},30~{S},32~{S},35~{R})-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.0^{4,9}]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl] 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate

Synonym

CCI-779; NSC 683864; rapamycin, 42-(3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate)

Shipping and Storage

Store Temp

4°C

Ship Temp

Ambient

Downloads

MSDS

T176503 MSDS PDF

Info Sheet

T176503 Info Sheet PDF

References

Geoerger B, Kerr K, Tang CB, et al. Antitumor activity of the rapamycin analog CCI-779 in human primitive neuroectodermal tumor/medulloblastoma models as single agent and in combination chemotherapy. Cancer Res. 2001 Feb 15;61(4):1527-1532. PMID: 11245461.

Gera JF, Mellinghoff IK, Shi Y, et al. AKT activity determines sensitivity to mammalian target of rapamycin (mTOR) inhibitors by regulating cyclin D1 and c-myc expression. J Biol Chem. 2004 Jan 23;279(4):2737-2746. PMID: 14576155.

Okui T, Shimo T, Fukazawa T, et al. Antitumor effect of temsirolimus against oral squamous cell carcinoma associated with bone destruction. Mol Cancer Ther. 2010 Nov;9(11):2960-2969. PMID: 20858724.

Siracusa R, Paterniti I, Cordaro M, et al. Neuroprotective effects of temsirolimus in animal models of Parkinson’s disease. Mol Neurobiol. 2018 Mar;55(3):2403-2419. PMID: 28357809.

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

  • M1676

    Methotrexate Hydrate

    DHF reductase inhibitor.

    ≥98%
  • U8000

    U-74389G

    Antioxidant shown to improve renal function.

    ≥95%
  • N1769

    Nerolidol, synthetic

    AChE inhibitor, F0F1-ATP synthase modulator.

    A mixture of cis and trans isomers, ≥96%
  • E6245

    Eplerenone

    Mineralocorticoid antagonist.

    ≥99%
  • N5550

    Nomilin

    Triterpene found in species of Citrus; HIV-1 pr...

    ≥98%
  • L1780

    Levocetirizine Dihydrochloride

    L-isomer of cetirizine; histamine H1 antagonist...

    ≥98%
  • I5753

    Ionomycin Calcium

    Polyether Ca2+ ionophore.

    ≥98%
  • C0020

    Cafestol

    Diterpene found in brewed, unfiltered coffee; F...

    ≥98%
  • A5280

    Angiotensin II (3-8), human

    Endogenous peptide fragment, involved in vasoco...

    ≥95%
  • T9969

    Tyrphostin AG490

    JAK2 inhibitor, potential EGFR inhibitor.

    ≥98%
  • L3551

    Limonin Glucoside

    Furanolactone found in Citrus.

    ≥95%
  • V1870

    Verruculogen

    Mycotoxin produced by Aspergillus; BK K+ channe...

    ≥95%
  • T2934

    Thiamphenicol Palmitate

    Chloramphenicol derivative; protein translation...

    ≥98%
  • A9662

    AZ-628

    B-Raf and c-Raf inhibitor.

    ≥96%
  • S1607

    Secretin, rat

    Endogenous peptide hormone, involved in feeding...

    ≥95%
  • N1894

    Nexturastat A

    HDAC6 inhibitor.

    ≥98%
  • M5793

    Moxifloxacin Free Base

    Fluoroquinolone; topoisomerase IV, topoisomeras...

    ≥98%
  • D3219

    Diflubenzuron

    Benzoylurea, insect growth regulator; chitin sy...

    ≥95%
  • P1770

    Perillyl Alcohol

    Terpene found in various plant and fruit source...

    ≥95%
  • C9809

    Cyclopiazonic Acid

    SERCA inhibitor.

    ≥98%, TLC

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