Date published: 2025-12-5

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FTI-277 trifluoroacetate salt (CAS 170006-73-2 (free base))

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Application:
FTI-277 trifluoroacetate salt is a peptidomimetic farnesyl transferase inhibitor
CAS Number:
170006-73-2 (free base)
Purity:
≥95%
Molecular Weight:
447.61
Molecular Formula:
C22H29N3O3S2•xC2HF3O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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FTI-277 trifluoroacetate salt is an inhibitor of farnesyl transferase (FTase). Studies show the compound to be a highly potent Ras CAAX peptidomimetic which antagonizes both H- and K-Ras oncogenic signaling. It is used in scientific research for its ability to inhibit the activity of farnesyltransferase, an enzyme involved in protein prenylation. FTI-277 trifluoroacetate salt is the trifluoroacetate salt form of the compound. As a potent FTI, FTI-277 trifluoroacetate salt exerts its inhibitory effects on farnesyltransferase by binding to the enzyme and preventing the transfer of a farnesyl group to target proteins. This inhibition disrupts the normal signaling pathways regulated by farnesylated proteins, which are involved in various cellular processes such as cell proliferation and survival. In scientific research, FTI-277 trifluoroacetate salt is widely utilized to study the role of farnesyltransferase and farnesylation in different biological systems. It has been employed to investigate the impact of farnesyltransferase inhibition on cancer cells, as certain proteins involved in tumor growth and metastasis require farnesylation for their proper function. By inhibiting farnesyltransferase, FTI-277 trifluoroacetate salt shows potential as an anticancer agent by interfering with the signaling pathways that drive tumor progression.


FTI-277 trifluoroacetate salt (CAS 170006-73-2 (free base)) References

  1. The farnesyltransferase inhibitor FTI-277 suppresses the 24-kDa FGF2-induced radioresistance in HeLa cells expressing wild-type RAS.  |  Cohen-Jonathan, E., et al. 1999. Radiat Res. 152: 404-11. PMID: 10477917
  2. Targeting the mevalonate pathway is a novel therapeutic approach to inhibit oncogenic FoxM1 transcription factor in human hepatocellular carcinoma.  |  Ogura, S., et al. 2018. Oncotarget. 9: 21022-21035. PMID: 29765517
  3. The anti-tubercular activity of simvastatin is mediated by cholesterol-driven autophagy via the AMPK-mTORC1-TFEB axis.  |  Bruiners, N., et al. 2020. J Lipid Res. 61: 1617-1628. PMID: 32848049
  4. Depletion of essential isoprenoids and ER stress induction following acute liver-specific deletion of HMG-CoA reductase.  |  De Giorgi, M., et al. 2020. J Lipid Res. 61: 1675-1686. PMID: 33109681
  5. Amino Acids Enhance Polyubiquitination of Rheb and Its Binding to mTORC1 by Blocking Lysosomal ATXN3 Deubiquitinase Activity.  |  Yao, Y., et al. 2020. Mol Cell. 80: 437-451.e6. PMID: 33157014
  6. A stable hepatitis D virus-producing cell line for host target and drug discovery.  |  Bach, C., et al. 2023. Antiviral Res. 209: 105477. PMID: 36511319

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

FTI-277 trifluoroacetate salt, 1 mg

sc-215058
1 mg
$160.00

FTI-277 trifluoroacetate salt, 5 mg

sc-215058A
5 mg
$581.00