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Search Results for " farnesyltransferase inhibitor "
Targets Recommended: Transferase

28

抑制剂 & 化合物

1

天然产物

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Cat. No. Product Name Target Signaling Pathways
T2678 LB42708

Transferase Metabolism
LB42708 是一种口服有活力的特异性法尼基转移酶抑制剂。它对H-Ras、N-Ras 和K-Ras4B 的法尼基化均有抑制作用,其IC50分别为 0.8 nM、1.2 nM 和 2.0 nM。
T38050 CP-609754

Transferase Metabolism
CP-609754 是高效的、可逆的法尼基转移酶抑制剂,对重组人 H-Ras 和重组 K-Ras 法尼基化的 IC50分别为 0.57 ng/mL 和 46 ng/mL。CP-609754有潜在的抗癌作用。
T17102 Tipifarnib (S enantiomer)

Tipifarnib S enantiomer,(S)-(-)-R-115777,(S)-Tipifarnib,IND-58359 S enantiomer

Transferase Metabolism
Tipifarnib S enantiomer ((S)-(-)-R-115777) 是Tipifarnib 的 S 型对映体,它比 Tipifarnib 特性低。其中 Tipifarnib 是farnesyltransferase 高效特异性抑制剂,IC50=0.6 nM。
T27773L L-739750 2HCl

L-739750 2HCl(160141-08-2 Free base)

Transferase Metabolism
L-739750 2HCl 是一种有效的拟肽法尼基转移酶的抑制剂,是一种新型假肽模拟物,具有潜在的抗癌活性。
T2700 FTI-277 hydrochloride

FTI 277 HCl

Apoptosis; Transferase; Ras Apoptosis; GPCR/G Protein; MAPK; Metabolism
FTI-277 hydrochloride (FTI 277 HCl) 是一种法尼基转移酶FTase 抑制剂,高效 Ras CAAX 肽模拟物,可抑制H-Ras 和K-Ras 信号转导,还可抑制hepatitis delta virus 感染。
T24273 Kurasoin B

Kurasoin-B

Others Others
Kurasoin B is an inhibitor of protein farnesyltransferase.
T24351 L 731735

L-731,735,L731735,L-731735,L731,735,L 731,735

Others Others
L 731735 is a farnesyltransferase inhibitor.
T15770 (Rac)-CP-609754

LNK754

Influenza Virus Microbiology/Virology
LNK754 is a farnesyltransferase inhibitor. It is used for the treatment of cancer and Alzheimer's disease.
T27773 L-739750

Others Others
L-739,750 is an inhibitor (FTI) of peptidomimetic farnesyltransferase.
T40331 Ftase inhibitor III

Others Others
Ftase Inhibitor III, derived from a phenotypic screen, functions as an anion-dependent inhibitor of Farnesyltransferase.
T71375 FTI-2600

Others Others
FTI-2600 is a farnesyltransferase inhibitor.
T24350 L 731734

L-731,734,L 731,734,L731734,L731,734,L-731734

Others Others
L 731734 is a farnesyltransferase inhibitor.
T11331L FTI 276

Others Others
FTI-276 is an inhibitor of protein farnesyltransferase (PFT) (IC50s: 0.9 and 0.5 nM for Plasmodium falciparum and human).
T69710 LB42908

Others Others
LB42908 is a highly potent Ras farnesyltransferase inhibitor(IC(50)=0.9 nM against H-Ras and 2.4 nM against K-Ras) with potential anticancer activity.
T25939 Pepticinnamin E

Others Others
Pepticinnamin E is a naturally occurring bisubstrate farnesyltransferase inhibitor.
T70372 FTI-249

Others Others
FTI-249 is a Farnesyltransferase inhibitor, which potently inhibited FTase (IC50 = 100–200 nM).
T70554 Chaetomellic acid A

Others Others
Chaetomellic acid A is a potent inhibitor of farnesyltransferase in isolated enzyme assays (IC50=55nM) but is inactive in whole cells. Inhibition of farnesyltransferase is selective over geranylgeranyltransferase I and II (IC50=92µM and 34µM respectively).
T70405 L-744832

Others Others
L-744832, also known as L-744,832, is a potent Farnesyltransferase inhibitor with potential anticancer activity.
T68923 FTI-2628

Others Others
FTI-2628 is a novel inhibitor of protein farnesyltransferase (FT), inhibiting the growth of P. falciparum in red blood cells and suppressing parasitemia.
T68227 BMS-214662 HCl

Others Others
BMS-214662 is a Farnesyltransferase inhibitor , is also a nonsedating benzodiazepine derivative with potential antineoplastic activity. BMS-214662 inhibits the enzyme farnesyltransferase and the post-translational farnesylation of number of proteins involved in signal transduction, which may result in the inhibition of Ras function and apoptosis in susceptible tumor cells. This agent may reverse the malignant phenotype of H-Ras-transformed cells and has been shown to be active against tumor cell...
T15353 FTI-2153

Others Others
FTI-2153 is a potent and highly selective farnesyltransferase (FTase) inhibitor (IC50: 1.4 nM). FTI-2153 is >3000-fold more potent at blocking H-Ras (IC50, 10 nM) than Rap1A processing.
T64101 FTI-2153 TFA

Others Others
FTI-2153 TFA 是一种高选择性的、有效的法尼基转移酶 farnesyltransferase (FTase) 抑制剂 (IC50: 1.4 nM)。FTI-2153 TFA 可有效抑制 H-Ras 蛋白的加工修饰 (IC50: 10 nM),对其抑制活性是对 Rap1A 蛋白加工的 3000 多倍。
T69993 BIM-46068

Others Others
BIM-46068 is a potent and specific inhibitor of human farnesyltransferase. In regard to a panel of cell lines, using the Compare analysis to determine the Pearson coefficient correlation, the anti-proliferative spectrum of BIM-46068 has been shown to be distinct from the profile of typical chemotherapeutic agents.
T69994 BIM-46050

Others Others
BIM-46050 is a potent and specific inhibitor of human farnesyltransferase. BIM-46050 is free acidic form of BIM-46068. The IC50 values for in vitro inhibition of human brain FTase indicate that BIM-46050 and the ester form BIM-46068 are potent inhibitors of farnesyltransferase. Their potencies are in the nanomolar range and compare favorably with the compounds B581, FTI-277 and L745,631. B581 is an analog of the tetrapeptide Cys-Val-Phe-Met obtained by replacement of the amino-terminal amide bon...
T62675 FTI-277

Others Others
FTI-277 是一种法尼基转移酶 FTase 抑制剂,也是一种高效 Ras CAAX 肽模拟物。FTI-277 对 H-Ras 和 K-Ras 信号转导具有抑制作用,能够抑制 hepatitis delta virus (HDV) 感染。
T70287 BMS-186511

Others Others
BMS-186511 is a Farnesyltransferase (FT) inhibitor with potential anticancer activity. BMS-186511 is a bisubstrate analogue inhibitor of FT, would inhibit the malignant growth properties of a cell line established from malignant schwannoma of an NF1 patient. Following treatment with BMS-186511 , ST88-14 cells became flat, nonrefractile, were contact-inhibited, and lost their ability to grow in soft agar. BMS-186511 was found to specifically inhibit FT, but not geranylgeranyltransferase I, a clos...
T85180 GGTI 2133 TFA

Others Others
GGTI 2133, a peptidomimetic inhibitor of geranylgeranyl transferase type I (GGTase I; IC50= 38 nM), exhibits 140-fold selectivity towards GGTase I compared to farnesyltransferase (IC50= 5,400 nM). The compound effectively inhibits the geranylgeranylation of RAP1A (IC50= 10 µM) without affecting the farnesylation of H-Ras (IC50= >30 µM). Moreover, GGTI 2133 reduces the growth, migration, and invasion of oral squamous cell carcinoma (OSSC) cells to 75, 45, and 27% of control levels, respectively. ...
T10512 Prenyl-IN-1

Transferase Metabolism
Prenyl-IN-1 是一种具有有效性和选择性的 prenylation 抑制剂,对香叶烯基转移酶 (geranylgeranyltransferase) 或法尼基转移酶 (farnesyltransferase) 具有抑制作用。Prenyl-IN-1 在帕金森模型中显示出抗氧化应激作用。

化合物

LB42708
Cat.No: T2678
Synonym:
Target: Transferase
CP-609754
Cat.No: T38050
Synonym:
Target: Transferase
Tipifarnib (S enantiomer)
Cat.No: T17102
Synonym: Tipifarnib S enantiomer,(S)-(-)-R-115777,(S)-Tipifarnib,IND-58359 S enantiomer
Target: Transferase
L-739750 2HCl
Cat.No: T27773L
Synonym: L-739750 2HCl(160141-08-2 Free base)
Target: Transferase
FTI-277 hydrochloride
Cat.No: T2700
Synonym: FTI 277 HCl
Target: Apoptosis, Transferase, Ras
Kurasoin B
Cat.No: T24273
Synonym: Kurasoin-B
Target: Others
L 731735
Cat.No: T24351
Synonym: L-731,735,L731735,L-731735,L731,735,L 731,735
Target: Others
(Rac)-CP-609754
Cat.No: T15770
Synonym: LNK754
Target: Influenza Virus
L-739750
Cat.No: T27773
Synonym:
Target: Others
Ftase inhibitor III
Cat.No: T40331
Synonym:
Target: Others
FTI-2600
Cat.No: T71375
Synonym:
Target: Others
L 731734
Cat.No: T24350
Synonym: L-731,734,L 731,734,L731734,L731,734,L-731734
Target: Others
FTI 276
Cat.No: T11331L
Synonym:
Target: Others
LB42908
Cat.No: T69710
Synonym:
Target: Others
Pepticinnamin E
Cat.No: T25939
Synonym:
Target: Others
FTI-249
Cat.No: T70372
Synonym:
Target: Others
Chaetomellic acid A
Cat.No: T70554
Synonym:
Target: Others
L-744832
Cat.No: T70405
Synonym:
Target: Others
FTI-2628
Cat.No: T68923
Synonym:
Target: Others
BMS-214662 HCl
Cat.No: T68227
Synonym:
Target: Others
FTI-2153
Cat.No: T15353
Synonym:
Target: Others
FTI-2153 TFA
Cat.No: T64101
Synonym:
Target: Others
BIM-46068
Cat.No: T69993
Synonym:
Target: Others
BIM-46050
Cat.No: T69994
Synonym:
Target: Others
FTI-277
Cat.No: T62675
Synonym:
Target: Others
BMS-186511
Cat.No: T70287
Synonym:
Target: Others
GGTI 2133 TFA
Cat.No: T85180
Synonym:
Target: Others
Prenyl-IN-1
Cat.No: T10512
Synonym:
Target: Transferase
Cat. No. Product Name Target Signaling Pathways
T16011 Manumycin A

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
Manumycin A is an antibiotic. Manumycin A induces apoptosis and exerts antitumor activity. Manumycin A inhibits exosome biogenesis and secretion via targeted inhibition of Ras/Raf/ERK1/2 signaling. Manumycin A acts as a selective, competitive inhibitor of

天然产物

Manumycin A
Cat.No: T16011
Synonym:
Target: Prostaglandin Receptor
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