ライフサイエンスコーパス: nitrobenzoate

1 ation with Ellman's reagent 5,5'-dithiobis(2-nitrobenzoate).

2 4,4'-dipyridyl disulfide or 5,5'-dithiobis(2-nitrobenzoate).

3 ples are 4-chlorophenyl and 4-bromophenyl 4'-nitrobenzoate.

4 nate and nitroethane and the inhibition by m-nitrobenzoate.

5 s by collisional activation of o-, m-, and p-nitrobenzoate.

6 allyl and 3-(4-chlorophenyl)-1-phenylallyl 4-nitrobenzoates.

7 etics of the native enzyme toward glycidyl-4-nitrobenzoates, 1, indicate the rate-limiting step in th

8 /[3 + 2] nitroalkene cycloaddition involving nitrobenzoate 13, chiral vinyl ether 16c, and vinyl sila

9 d using Ellman's reagent, 5,5'-dithio-bis (2-nitrobenzoate) (3), to detect the resulting thiols.

10 matic compounds, such as the conversion of 4-nitrobenzoate (4-NBA) to protocatechuate by the bacteria

11 quantified using the chromophore 4-hydroxy-3-nitrobenzoate (4H3N).

12 x-electron oxidation of p-aminobenzoate to p-nitrobenzoate and contains the EX2HX60-180EX2H sequence

13 ed to the elimination of 2 equiv of 5-thio-2-nitrobenzoate and partial recovery of activity.

14 (Ar-NH(2), where Ar = 4-carboxyphenyl) to p-nitrobenzoate (Ar-NO(2)) in the biosynthesis of the anti

15 n the NADPH-dependent DTNB [5,5'-dithiobis(2-nitrobenzoate)] assay.

16 -benzotriazin-4(3H)-one]yl)-5,5'-dithiobis-2-nitrobenzoate (BDTNB), and displacement with glutathione

17 When either 5-thio-2-nitrobenzoate-derivatized C16S or C55S PRK, as mimics of

18 e corresponding S-nitrosothiols and 5-thio-2-nitrobenzoate dianion.

19 (NEM), and to a lesser extent, dithio(bis)-p-nitrobenzoate (DTNB), improved the heat stability of WPI

20 he thiol-modifying reagents 5,5-dithiobis (2-nitrobenzoate) (DTNB) and methyl methanethiosulfonate (M

21 tein sulfhydryl groups with 5,5'-dithiobis(2-nitrobenzoate) (DTNB) under carefully controlled conditi

22 nethiolsulfonate (MMTS) and 5,5'-dithiobis(2-nitrobenzoate) (DTNB), including the appropriate Cys -->

23 urified amidase contained 11 5,5-dithiobis(2-nitrobenzoate) (DTNB)-titratable sulfhydryl (SH) groups.

24 The dianions of p-cyano- and p-nitrobenzoate esters are rather stable on the voltammetr

25 thyl L-glutamate with methyl 2-bromomethyl-4-nitrobenzoate followed by catalytic reduction of the nit

26 to induce stereoelectronic effects (fluoro, nitrobenzoate), handles for heteronuclear NMR ((19)F:flu

27 ivative of aldol adduct 1b and the 2-bromo-5-nitrobenzoate of 3b, which were established by single-cr

28 above synthetic route produced the 17 beta-p-nitrobenzoate of 7 alpha-[125I]IDHT in carrier-free form

29 e, oxidoreductases can transform PNBM into 4-nitrobenzoate (PNBA).

30 ron oxidation of p-aminobenzoate (pABA) to p-nitrobenzoate (pNBA).

31 ucture revealed an exo ring pucker, with the nitrobenzoate pseudoaxial on the pyrrolidine envelope an

32 The S-nitroso derivative of 5-thio-2-nitrobenzoate was synthesized from 5,5'-dithiobis(2-nitr

33 (2S,4R)-4-Hydroxyproline(4-nitrobenzoate) was synthesized.

34 The reaction of DGD with dithiobis(nitrobenzoate) was used to probe the preexisting forms o

35 astic crystals, of the type 4-bromophenyl 4'-nitrobenzoate where the halogen bonding and C-H...O hydr