T-8123 Trametinib, >99%

Synonyms : [GSK-1120212] [JTP-74057]

Related Terms : [Mekinist]

  • Size
  • US $
  • £
  • ¥
  • 10 mg
  • 38
  • 34
  • 29
  • 6,000
  • Add to Cart Qty:
  • In stock
  • 25 mg
  • 60
  • 55
  • 46
  • 9,500
  • Add to Cart Qty:
  • In stock
  • 50 mg
  • 73
  • 67
  • 56
  • 11,500
  • Add to Cart Qty:
  • In stock
  • 100 mg
  • 99
  • 90
  • 76
  • 15,700
  • Add to Cart Qty:
  • In stock
  • 200 mg
  • 134
  • 123
  • 103
  • 21,200
  • Add to Cart Qty:
  • In stock
  • 250 mg
  • 155
  • 142
  • 119
  • 24,500
  • Add to Cart Qty:
  • In stock
  • 500 mg
  • 285
  • 261
  • 219
  • 45,100
  • Add to Cart Qty:
  • In stock
  • 1 g
  • 483
  • 443
  • 372
  • 76,400
  • Add to Cart Qty:
  • In stock
  • 2 g
  • 894
  • 820
  • 689
  • 141,300
  • Add to Cart Qty:
  • In stock
  • 5 g
  • 1,770
  • 1,624
  • 1,364
  • 279,800
  • Add to Cart Qty:
  • In stock

Note: Our Euro, Pound, and Yen prices are revised regularly to account for currency exchange rate fluctuations.

To receive a Formal Quotation for catalog sizes of this product and/or any other products, please add them to your shopping cart and click on the “REQUEST A QUOTATION” box.
Click Here to Request a Quotation for Larger Quantities Free Shipping and Handling to the U.S. and 32 Other Countries
  • M.W. 615.39
  • C26H23FIN5O4
  • [871700-17-3]

Storage: Store at or below -20 ºC. Solubility: Soluble in DMSO at 20 mg/mL with warming; very poorly soluble in ethanol; very poorly soluble in water; maximum solubility in plain water is estimated to be about 5-10 µM; buffers, serum, or other additives may increase or decrease the aqueous solubility. Disposal: A.

Select Lot Number to view Certificate of Analysis

View the SDS for this product

  • More than 220 labs worldwide have purchased Trametinib from LC Labs (either directly from us or from our many distributors, many of whom resell under their own labels).
  • Trametinib is a selective MEK inhibitor.
  • Trametinib inhibited MEK1/2 kinase activity, prevented Raf-dependent MEK phosphorylation, and produced prolonged p-ERK1/2 inhibition. It blocked the cell growth potently in most tumor lines with mutant BRAF or Ras. In xenograft tumor models, trametinib inhibited tumor growth, possibly by sustained suppression of p-ERK1/2, inhibition of tumor Ki67, and stimulation of p27Kip1/CDKN1B. The largest antitumor effect in vivo was among tumors harboring mutant BRAF or Ras. Gilmartin, A.G., et al. "GSK1120212 (JTP-74057) is an inhibitor of MEK activity and activation with favorable pharmacokinetic properties for sustained in vivo pathway inhibition." Clin. Cancer Res. 17: 989-1000 (2011).
  • A phase 1 clinical trial demonstrated substantial clinical activity of trametinib in human melanoma. Falchook, G.S., et al. "Activity of the oral MEK inhibitor trametinib in patients with advanced melanoma: a phase 1 dose-escalation trial." Lancet Oncol. 13: 782-789 (2012).
  • Trametinib improved rates of progression-free and overall survival among patients who had metastatic melanoma with a BRAF V600E or V600K mutation when compared with dacarbazine or paclitaxel. Flaherty, K.T., et al. "Improved survival with MEK inhibition in BRAF-mutated melanoma." N. Engl. J. Med. 367: 107-114 (2012).
  • Both trametinib and leflunomide can suppress adjuvant-induced arthritis (AIA) and type II collagen-induced arthritis (CIA) development completely. In the CIA model, trametinib, but not leflunomide, inhibited collagen-reactive T-cell proliferation ex vivo, whereas leflunomide, but not trametinib, inhibited anti-collagen antibody production. Yamaguchi, T., et al. "Suppressive effect of an orally active MEK1/2 inhibitor in two different animal models for rheumatoid arthritis: a comparison with leflunomide." Inflamm. Res. 61: 445-454 (2012).
  • For solid tumors, RAF/RAS mutation and the expression of the DUSP6 gene were strong predictors of sensitivity to trametinib. Among hematologic cell lines, acute and chronic myeloid leukemia cell lines were particularly sensitive to trametinib. Jing, J., et al. "Comprehensive predictive biomarker analysis for MEK inhibitor GSK1120212." Mol. Cancer Ther. 11: 720-729 (2012).
  • Trametinib had favorable antitumor activities against colorectal cancers in vitro and in vivo. It exhibited an additive or a synergistic effect in combination with other chemotherapy agents including 5-fluorouracil, oxaliplatin, or SN-38. Yamaguchi, T., et al. "Antitumor activities of JTP-74057 (GSK1120212), a novel MEK1/2 inhibitor, on colorectal cancer cell lines in vitro and in vivo." Int. J. Oncol. 39: 23-31 (2011).
  • Related CAS number: 1187431-43-1 for the dimethylsulfoxide solvate of trametinib.
  • Another CAS number previously assigned to Trametinib, namely 1204531-14-5, has been deleted by CAS and is no longer in use.
  • Trametinib (as the dimethyl sulfoxide) is the active ingredient in the drug product sold under the trade name Mekinist®.  This drug is currently approved in a least one country for the treatment of patients with unresectable or metastatic melanoma with BRAF V600E or V600K mutations.  NOTE:  THE TRAMETINIB SOLD BY LC LABORATORIES FOR RESEARCH IS NOT MEKINIST®, AND IS NOT FOR HUMAN USE.
  • Sold for laboratory or manufacturing purposes only; not for human, veterinary, food, or household use.
  • This product is offered for R&D use in accordance with (i) 35 USC 271(e)+A13(1) in the U.S.; (ii) Section 69.1 of Japanese Patent Law in Japan; (iii) Section 11, No. 2 of the German Patent Act of 1981 in Germany; (iv) Section 60, Paragraph 5b of the U.K. Patents Act of 1977 in the U.K.; (v) Sections 55.2(1) and 55.2(6) and other common law exemptions of Canadian patent law; (vi) Section 68B of the Patents Act of 1953 in New Zealand together with the amendment of same by the Statutes Amendment Bill of 2002; (vii) such related legislation and/or case law as may be or become applicable in the aforementioned countries; and (viii) such similar laws and rules as may apply in various other countries.
  • Not available in some countries; not available to some institutions; not available for some uses.