FTase Inhibitor I

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Names

[ CAS No. ]:
149759-96-6

[ Name ]:
FTase Inhibitor I

[Synonym ]:
(2S)-2-[[(2S)-2-[[(2S)-2-[[(2R)-2-amino-3-sulfanylpropyl]amino]-3-methylbutyl]amino]-3-phenylpropanoyl]amino]-4-methylsulfanylbutanoic acid
B581

Chemical & Physical Properties

[ Density]:
1.161g/cm3

[ Boiling Point ]:
716.1ºC at 760mmHg

[ Molecular Formula ]:
C22H38N4O3S2

[ Molecular Weight ]:
470.69

[ Flash Point ]:
386.9ºC

[ Exact Mass ]:
470.23900

[ PSA ]:
180.58000

[ LogP ]:
3.25410

[ Appearance of Characters ]:
solid | white

[ Vapour Pressure ]:
1.6E-21mmHg at 25°C

[ Index of Refraction ]:
1.566

[ Storage condition ]:
−20°C

[ Water Solubility ]:
H2O: soluble

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

[Anti tumor activity of farnesyl transferase inhibitor].

Gan To Kagaku Ryoho. 24(2) , 145-55, (1997)

Posttranslational farnesylation by farnesyltransferase (FTase) is critical for the function of ras oncogene product and FTase has attracted attention as the new target of anticancer agents. B956 and B...

Bcl-2 differentially targets K-, N-, and H-Ras to mitochondria in IL-2 supplemented or deprived cells: implications in prevention of apoptosis.

Oncogene 18(35) , 4930-9, (1999)

IL-2 deprivation triggers apoptosis in the murine T cell line TS1alphabeta, a process that can be blocked by overexpression of Bcl-2. Here we show that Bcl-2 and Ras proteins interact in mitochondria ...

Peptidomimetic inhibitors of Ras farnesylation and function in whole cells.

J. Biol. Chem. 268(25) , 18415-8, (1993)

The ras protooncogene is involved in regulation of cell growth. Mutations that activate the protein result in uncontrolled cell growth. Ras undergoes a series of posttranslational processing events, t...


More Articles

Related Compounds

  • FTase Inhibitor II
  • ftase inhibitor iv
  • Ftase inhibitor III
  • Aromatase Inhibitor I
  • Wee1 Inhibitor I
  • trypsin inhibitor I, Lycopersiconperuvianum
  • (2-phenyl-2H-1,2,3-triazol-4-yl)(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidin-1-yl)methanone
  • (4-methyl-2-(1H-pyrrol-1-yl)thiazol-5-yl)(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidin-1-yl)methanone
  • 3-[1-(2-Phenyl-1,3-thiazole-4-carbonyl)pyrrolidin-3-yl]-5-(trifluoromethyl)-1,2,4-oxadiazole
  • (E)-3-(furan-2-yl)-1-(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidin-1-yl)prop-2-en-1-one
  • (7-Methoxybenzofuran-2-yl)(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidin-1-yl)methanone
  • (2-Methylthiazol-4-yl)(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidin-1-yl)methanone
  • 2-methyl-6-(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidine-1-carbonyl)pyridazin-3(2H)-one
  • 2-(1-methyl-1H-indol-3-yl)-1-(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidin-1-yl)ethanone
  • Benzo[d]thiazol-6-yl(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidin-1-yl)methanone
  • Benzo[d][1,3]dioxol-5-yl(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)pyrrolidin-1-yl)methanone
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