20 Results for "

protein farnesyltransferase

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "protein farnesyltransferase" in MCE Product Catalog:

Cat. No.: HY-15873A
CAS No.: 1217471-51-6
Purity:  98.03%
Research Areas:  

Cancer

FTI 276 TFA is a farnesyltransferase (FTase) inhibitor with an IC50 of 0.5 nM, and it exhibits selectivity for FTase over geranylgeranyltransferase I (GGTase I). FTI 276 TFA blocks the farnesylation of H-Ras and K-Ras4B, causes inactive Ras-Raf complexes to accumulate in the cytoplasm, and inhibits constitutive MAPK activation. FTI 276 TFA reduces the number, incidence and volume of tumors, and restricts the growth of tumors expressing activated K-ras. FTI 276 TFA can be used in research related to pulmonary adenoma .
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Cat. No.: HY-118563
CAS No.: 135784-48-4
Farnesylthioacetic acid is a competitive, non-substrate inhibitor of Prenylcysteine α-carboxyl methyltransferase. It acts as a non-substrate competitive inhibitor of Arabidopsis thaliana Prenylcysteine α-carboxyl methyltransferase and blocks methyltransferase activity. Farnesylthioacetic acid does not inhibit protein farnesyltransferase activity in Arabidopsis. It induces Apoptosis. Farnesylthioacetic acid regulates the subcellular localization of Ras protein, reducing the proportion of cytoplasmic Ras protein without disrupting membrane binding. It enhances ABA-induced seed dormancy, delays seed germination, and promotes maximum stomatal closure at lower exogenous ABA concentrations. Farnesylthioacetic acid can be used in studies related to promyelocytic leukemia .
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Cat. No.: HY-16111A
CAS No.: 195981-08-9
Research Areas:  

Cancer

BMS-214662 hydrochloride is an inhibitor of farnesyltransferase (Farnesyl Transferase). BMS-214662 hydrochloride can effectively block the localization and function of Ras proteins on the cell membrane by inhibiting the prenylation modification of Ras proteins, thereby exerting anti-tumor activity. The IC50 value of BMS-214662 hydrochloride for H-Ras is 1.3 nM, and for K-Ras it is 8.4 nM. BMS-214662 hydrochloride can be used in the research of tumor diseases related to Ras .
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Cat. No.: HY-15872
CAS No.: 170006-73-2
FTI-277 is a farnesyltransferase (FTase) inhibitor. FTI-277 inhibits Ras farnesylation, blocks the phosphorylation of downstream ERK1/2 and mTOR, and reduces membrane-bound active N-ras protein. FTI-277 activates caspase 3, upregulates Bim expression, induces cell apoptosis, suppresses regulatory T cell expansion, enhances macrophage phagocytosis, and improves bacterial clearance. FTI-277 activates the PI3K/Akt signaling pathway, inhibits osteoblast differentiation, and reduces the proliferation ability of neuroblastoma cells. FTI-277 can be used in research related to head and neck squamous cell carcinoma, neuroblastoma, sepsis, and vascular calcification .
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Cat. No.: HY-110038
CAS No.: 1217447-06-7
FTI-277 TFA is a farnesyltransferase (FTase) inhibitor. FTI-277 TFA inhibits Ras farnesylation, blocks the phosphorylation of downstream ERK1/2 and mTOR, and reduces membrane-bound active N-ras protein. FTI-277 TFA activates caspase 3, upregulates Bim expression, induces cell apoptosis, suppresses regulatory T cell expansion, enhances macrophage phagocytosis, and improves bacterial clearance. FTI-277 TFA activates the PI3K/Akt signaling pathway, inhibits osteoblast differentiation, and reduces the proliferation ability of neuroblastoma cells. FTI-277 TFA can be used in research related to head and neck squamous cell carcinoma, neuroblastoma, sepsis, and vascular calcification .
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Cat. No.: HY-116254
CAS No.: 160141-08-2
Target:  

Farnesyl Transferase

Research Areas:  

Others

L-739750 is a selective protein farnesyltransferase (PFTase) inhibitor (IC50: 0.4 nM). PFTase utilizes farnesyl diphosphate to farnesylate the cysteine residue of protein substrates having a C-terminal CAAX motif. L-739750 is a selective CAAX peptidomimetic .
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Cat. No.: HY-151566
CAS No.: 2842067-19-8
Research Areas:  

Infection

Antifungal agent 46 (compound 2f) is a potent antifungal agent. Antifungal agent 46 prevents Ras signaling by inhibiting protein farnesyltransferase .
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Cat. No.: HY-U00327
CAS No.: 360561-53-1
Research Areas:  

Neurological Disease

Prenyl-IN-1 is a protein prenylation inhibitor, especially a geranylgeranyltransferase (GGT) or a farnesyltransferase (FT) inhibitor, exhibiting potent activity against oxidative stress, and particularly in the treatment of Parkinson's Disease.
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Cat. No.: HY-117893
CAS No.: 201487-53-8
Research Areas:  

Cancer

BIM-46068 is a potent, selectively human brain Farnesyltransferase (FTase) inhibitor (IC50 = 91.4 nM). BIM-46068 can specifically inhibit Ras processing in MiaPaCa-2 cancer cells. BIM-46068 can be used for the study of pancreatic cancer .
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Cat. No.: HY-N13874
CAS No.: 174232-43-0
Andrastin C is a protein farnesyltransferase inhibitor. Andrastin C has a common androstane skeleton .
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Cat. No.: HY-N13876
CAS No.: 184432-08-4
Andrastin D is a protein farnesyltransferase inhibitor. Andrastin D has a common androstane skeleton .
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Cat. No.: HY-N9604
CAS No.: 174232-44-1
Target:  

Farnesyl Transferase

Research Areas:  

Cancer

Andrastin B is a protein farnesyltransferase inhibitor. Andrastin B has a common androstane skeleton .
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Cat. No.: HY-122469
CAS No.: 193696-42-3
Target:  

Farnesyl Transferase

Research Areas:  

Cancer

Kurasoin B is a protein farnesyltransferase inhibitor (IC50: 58.7 μM). Kurasoin B can be produced by Paecilomyces sp. FO-3684 .
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Cat. No.: HY-P701885
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: FNTA; Type I protein Geranyl-Geranyltransferase Subunit Alpha; farnesyltransferase, CAAX Box, Subunit Alpha; CAAX farnesyltransferase Subunit Alpha; protein farnesyltransferase/Geranylgeranyltransferase Type-1 Subunit Alpha; farnesyltransferase, CAAX Box,
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P701886
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: FNTA; Type I protein Geranyl-Geranyltransferase Subunit Alpha; farnesyltransferase, CAAX Box, Subunit Alpha; CAAX farnesyltransferase Subunit Alpha; protein farnesyltransferase/Geranylgeranyltransferase Type-1 Subunit Alpha; farnesyltransferase, CAAX Box,
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P72193
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: FDFT1; Farnesyl-Diphosphate farnesyltransferase; Farnesyl-Diphosphate farnesyltransferase 1; Presqualene-Di-Diphosphate Synthase; SQS; Squalene Synthetase; Squalene Synthase; DGPT; FPP:FPP farnesyltransferase; ERG9; SS; SQSD
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P83099
Synonyms: FNTB; protein farnesyltransferase subunit beta; FTase-beta; CAAX farnesyltransferase subunit beta; Ras proteins prenyltransferase subunit beta

Host:  

Rabbit

Application:  

WB, IP

Reactivity:  

Human

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Cat. No.: HY-P83099A
Synonyms: FNTB; protein farnesyltransferase subunit beta; FTase-beta; CAAX farnesyltransferase subunit beta; Ras proteins prenyltransferase subunit beta

Host:  

Rabbit

Application:  

WB, IP

Reactivity:  

Human

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Cat. No.: HY-P88009
Synonyms: protein farnesyltransferase subunit beta, FTase-beta, CAAX farnesyltransferase subunit beta, Ras proteins prenyltransferase subunit beta, FNTB

Host:  

Rabbit

Application:  

WB, FC, ICC/IF

Reactivity:  

Human

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Cat. No.: HY-183421
CAS No.: 146016-64-0
Synonyms: Gliotoxin monoacetate
Acetylgliotoxin (Gliotoxin monoacetate) is a farnesyltransferase (FTase) inhibitor with an IC50 of 4.4 μM against human targets. Acetylgliotoxin inhibits the growth of fungal, bacterial, and viral pathogens; it binds to free protein thiols and induces ROS production. Acetylgliotoxin increases the survival rate of Caenorhabditis elegans infected with Candida albicans, but exhibits toxicity at higher concentrations. Acetylgliotoxin is applicable to research related to Candida albicans infections .
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