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Supplier NameMedChemExpress (MCE)
Contactsales
Tel609-228-6898
Mobile609-228-6898
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Emailsales@medchemexpress.com; tech@medchemexpress.com
Websitehttps://www.medchemexpress.com/
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Product NameFTI-277 (hydrochloride)
SynonymsFTI 277
CS-1757
FTI 277 HCl
FTI 277 HCL
FTI 277 HYDROCHLORIDE
FTI-277 (hydrochloride)
FTI-277 TRIFLUOROACETATE SALT

Synonyms

FTI 277
CS-1757
FTI 277 HCl
FTI 277 HCL
FTI 277 HYDROCHLORIDE
FTI-277 (hydrochloride)
FTI-277 TRIFLUOROACETATE SALT
4-[2(R)-amino-3-mercaptopropyl]amino-2-phenylbenzoyl-(S)-methionine methyl ester hydrochloride
(S)-methyl 2-(5-(((R)-2-amino-3-mercaptopropyl)amino)-[1,1'-biphenyl]-2-ylcarboxamido)-4-(methylthio)butanoate FTI 277 HCl
CAS180977-34-8
EINECS604-604-1
Chemical FormulaC22H30ClN3O3S2
Molecular Weight484.075
inchi
Package10 mM * 1 mL;1 mg;2 mg;5 mg;10 mg;50 mg
PriceEmail to quote
DescriptionsFTI-277 hydrochloride

FTI-277 hydrochloride

MedChemExpress (MCE)

HY-15872A

180977-34-8

98.29%

4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months

Descriptions

FTI-277 hydrochloride

FTI-277 hydrochloride

MedChemExpress (MCE)

HY-15872A

180977-34-8

98.29%

4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months
-20°C, 1 month (sealed storage, away from moisture)

Room temperature in continental US
may vary elsewhere.

FTI-277 hydrochloride is an inhibitor of farnesyl transferase (FTase)
a highly potent Ras CAAX peptidomimetic which antagonizes both H- and K-Ras oncogenic signaling. FTI-277 hydrochloride can inhibit hepatitis delta virus (HDV) infection.

Treatment with FTI-277 (20 microM) for 48 h prior to irradiation led to a significant decrease in survival of radioresistant cells expressing the 24-kDa isoform (HeLa 3A) but had no effect on the survival of control cells (HeLa PINA). The radiosensitizing effect of FTI-277 is accompanied by a stimulation of postmitotic cell death in HeLa 3A cells and by a reduction in G(2)/M-phase arrest in both cell types [1]. Treatment of PC-3 cells with GGTI-298 and FTI-277 inhibited migration and invasion in a time- and dose-dependent manner [3].

FTI-277 treatment prevented increased PTP-1B and PTEN protein expression in burned mice as compared with vehicle alone. In contrast, FTI-277 did not significantly alter protein expression of PTP-1B and PTEN in sham-burned mice [2].

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[1]. Cohen-Jonathan E, et al. The farnesyltransferase inhibitor FTI-277 suppresses the 24-kDa FGF2-induced radioresistance in HeLa cells expressing wild-type RAS. Radiat Res. 1999 Oct
152(4):404-11.
[Content Brief]

[2]. Nakazawa H, et al. Role of protein farnesylation in burn-induced metabolic derangements and insulin resistance in mouse skeletal muscle. PLoS One. 2015 Jan 16
10(1):e0116633.
[Content Brief]

[3]. Virtanen SS, et al. Inhibition of GGTase-I and FTase disrupts cytoskeletal organization of human PC-3 prostate cancer cells. Cell Biol Int. 2010 Aug
34(8):815-26.
[Content Brief]

[4]. Bordier BB, et al. A prenylation inhibitor prevents production of infectious hepatitis delta virus particles. J Virol. 2002 Oct
76(20):10465-72.
[Content Brief]

Supplier Websitehttps://www.medchemexpress.com/FTI-277-hydrochloride.html
Last Update2025-05-21 16:50:25
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