ライフサイエンスコーパス: butoxy

1 inhibitor, 3, 4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2H)-isoquinolinone (DPQ; IC50=1 microM/l) was

2 RP inhibitor 3,4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2H)-isoquinolinone both showed increased resis

3 er by 10 muM 3,4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2H)-isoquinolinone, an established PARP inhibi

4 RP inhibitor 3,4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2h)-isoquinolinone.

5 ic inhibitor 3,4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2h)-isoquinolinone.

6 ist (R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2-ethyl-phenyl}-propionic acid (20) for the trea

7 ble L-glutamic acid derivative, (4S)-5-(tert-butoxy)-4-[(tert-butoxycarbonyl)amino]-5- oxopentanoic a

8 tert-Butoxy-(4-phenyl-quinolin-3-yl)-acetic acids (tBPQA) are

9 odamine 6G dyes with tetrakis(perfluoro-tert-butoxy)aluminate counterions (~6000 dyes per NP), and be

10 The 5'-methoxy, 5'-ethoxy, and 5'-butoxy analogs of 2,5,6-trichloro-1-(beta-D-ribofuranosy

11 a methoxy group to form ethoxy, i-propoxy, s-butoxy, and t-butoxy groups on a p-aminobenzoate peptidy

12 f substituted toluenes with tert-butyl, tert-butoxy, and tert-butylperoxyl radicals are reanalyzed he

13 blocked by the pan-caspase inhibitor N-tert-butoxy-carbonyl-Val-Ala-Asp-fluoro methylketone (zVAD-fm

14 Three chiral alpha-(nonafluoro-tert-butoxy)carboxylic acids (R)-1, (RS)-2, (R)-3 were synthe

15 Paramagnetic (13)C NMR shifts of the butoxy chains as well as all (1)H NMR chemical shifts ar

16 ong the compounds studied, n-butyl- and/or n-butoxy-containing guanidines showed superior biological

17 t-membered ring in the anion radical of tert-butoxy-COT.

18 Compound 3, the butoxy derivative, had a lower target-to-nontarget ratio

19 performed at 120-130 degrees C, whereas tert-butoxy derivatives undergo the retro-ene reaction at 90

20 p to form ethoxy, i-propoxy, s-butoxy, and t-butoxy groups on a p-aminobenzoate peptidyl carrier prot

21 Butoxy increases in surface concentration over Pt(111) w

22 y at the 2'-ribose position linked through a butoxy linker.

23 fied a substituted quinazolinone (Quin-C1, 4-butoxy-N-[2-(4-methoxy-phenyl)-4-oxo-1,4-dihydro-2H-quin

24 opoxy group of 2c was preferred over ethoxy, butoxy, or pentoxy.

25 y-3-propyl-4-[4-[4-(2H-tetrazol-5-yl)phenoxy]butoxy]phenyl) ethanone (4).

26 These mechanistic data imply that the tert-butoxy radical reacts with the C-H bonds of alkanes, and

27 oportionation pathway, catalyzed by the tert-butoxy radical, of mixed peroxides for the formation of

28 cal traps support the intermediacy of a tert-butoxy radical, which forms an alkyl radical intermediat

29 is the C-H cleavage of cyclohexane by a tert-butoxy radical.

30 mply that C-H bond cleavage occurs by a tert-butoxy radical.

31 to vapors of trimethylaluminum and tris(tert-butoxy)silanol deposits highly conformal layers of amorp

32 d to monitor the rapid reaction of tris(tert-butoxy)silanol with triflic anhydride in a T(1) -correct

33 supported by sterically demanding tris(tert-butoxy)siloxide ligands induces a large cooperative effe

34 uced via grafting reactions of the tris(tert-butoxy)siloxy iron(III) complex Fe[OSi(O(t)Bu)(3)](3)(TH

35 The tris(tert-butoxy)siloxy titanium complexes Ti[OSi(O(t)Bu)(3)](4) (

36 ction between the methyl hydrogens on a tert-butoxy substituent and the cyclooctatetraene (COT) ring

37 mics of nickel(II) phthalocyanine with eight butoxy substituents, NiPc(OBu)8.

38 of sulfonyl halide derivatives of (S)-(tert-butoxy)-[(tert-butoxycarbonyl)amino]oxoalkanoic acids.

39 ,5-bis{4-[di(p-anisyl)amino]styryl}-3,4-di(n-butoxy)thiophene, [1](2+) and [2](2+) respectively.

40 ndium tin oxide (ITO) reacts with tetra(tert-butoxy)tin to give surface bound alkoxytin species.

41 [(R)-3,3'-dibromo-2,2'-binaphthoxy](di-tert-butoxy)titanium(IV) (R-3) exists as a crystallographic C

42 ) or pentane (17-19); OR(f) = perfluoro-tert-butoxy) via photolysis of the precursor complex [(HEB)Re