ライフサイエンスコーパス: NDA

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1 NDA cycloadducts were not obtained from other hydroxamic

2 NDA/CN- is placed in the inlet vial between the sampling

3 ments demonstrate that while the twisted 3,7-NDA-based P1 is a poor semiconductor, the planar 2,6-fun

4 range for the determination of amino acids, NDA can undergo reaction with OH- ions, but OPA does not

5 , which were trapped in nitroso-Diels-Alder (NDA) reactions with various dienes to afford the corresp

6 here we describe optimized fluorescamine and NDA derivatization reactions that enhance the accuracy o

7 n principle, the optimized fluorescamine and NDA microplate procedures reported here can be utilized

8 For both fluorescamine and NDA, we have shown that the RFI values of 16 of 19 amino

9 between GCL activities measured by HPLC and NDA-microtiter plate analyses.

10 sing the possible reaction mechanism between NDA and HCys.

11 ular, a specific neuropeptide, which we call NDA-1, contributes to the reduction of Gram-positive bac

12 the latter with naphthalene-2,3-dialdehyde (NDA) and quantification by reverse-phase high-performanc

13 a basic solution of naphthalene dialdehyde (NDA) and taurine.

14 camine and naphthalene-2,3-dicarboxaldehyde (NDA) have proven to be excellent fluorogenic reagents fo

15 tized with naphthalene-2,3-dicarboxaldehyde (NDA) was investigated using a combination of high-perfor

16 he reaction of naphthalene dicarboxaldehyde (NDA) with GSH or gamma-GC to form cyclized products that

17 stants 0.0018 s-1 for OPA and 0.0012 s-1 for NDA.

18 lts suggest that the degradation pathway for NDA derivatives is similar to the previously reported pa

19 (1-phenylethylurea) 3 (same conditions) gave NDA cycloadducts in high yields (97-99%) with no ene pro

20 luenediamine (6TDA), 1,5-naphthalenediamine (NDA), and p-phenylenediamine (PPDA) in human urine.

21 ino groups, 2,3-naphthalenedicarboxaldehyde (NDA) can selectively react with HCys to form a 6-membere

22 For 2,3-naphthalenedicarboxaldehyde (NDA) these values were estimated to be 15, 7, and 78%.

23 Under optimal NDA derivatization conditions, the SAHH-based probe show

24 of this method is evaluated, and the optimum NDA/CN- concentration and separation conditions for this

25 adation of the isoindole derivative L-serine-NDA-beta-mercaptoethanol was found to follow pseudo-firs

26 In aqueous solutions, NDA is less strongly hydrated than OPA.

27 osine-NDA and ceramidase-derived sphingosine-NDA were 9.6 and 12.3 fmol, respectively, and the limits

28 The limits of detection for sphingosine-NDA and ceramidase-derived sphingosine-NDA were 9.6 and

29 Finally, in photobleaching studies, NDA derivatives rapidly degraded into a variety of produ

30 The NDA and nitroso-ene reaction pathways of nitroso interme

31 reactive and that activation energies in the NDA processes are lower than the isomerization barriers

32 d to evaluate and compare the utility of the NDA method with an assay based on monobromobimane deriva

33 by the addition of beta-cyclodextrin to the NDA reaction.

34 sing sodium periodate, resulting in variable NDA yields (13-51%) from hydroxamic acids 1-10 with cycl

35 vage of SAH, the generated HCys reacted with NDA to form highly fluorescent products with a quantum y

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