ライフサイエンスコーパス: authentic sample

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1 FT calculations and by the preparation of an authentic sample.

2 as unambiguously assigned by comparison with authentic samples.

3 by using them to predict the identity of new authentic samples.

4 y Fe(II)/ascorbic acid through spiking in of authentic samples.

5 ion products were confirmed by comparison to authentic samples.

6 mined by total synthesis and comparison with authentic samples.

7 nfirm the relationship between the model and authentic samples.

8 ilic and aqueous extracts of 20 monovarietal authentic samples.

9 ivative with Marfey's reagent and that of an authentic sample (7) obtained by enantiospecific synthes

10 In the authentic samples, 73% of all 777 drug intakes were dete

11 ions were detectable in the ESI(-)-MS of the authentic samples aged in oak (m/z 197, 241, 301 and 307

12 ble differences between the ESI(-)-MS of the authentic samples (aged in oak or amburana casks) and th

13 These authentic samples allowed the definition of a confidence

14 as validated with an independent test set of authentic samples belonging to the seven selected brands

15 taste differences between counterfeited and authentic samples but the assessors were unable to corre

16 Obtaining an authentic sample containing 2uPFOA and 2HPFOA, we optimi

17 The results from analysis of authentic samples demonstrated that the SPE-UPLC-MS/MS m

18 X-ray studies and syntheses of authentic samples establish that the published assignmen

19 MS, (1)H and (13)C NMR, and comparison to an authentic sample made by reaction of MeGeCl(3) with NaOM

20 ate the transient anhydride 5 en route to an authentic sample of 4.

21 An authentic sample of obtusallene V was studied by NMR spe

22 orted by voltammetric investigations with an authentic sample of the anionic [AuI2](-) complex.

23 ynthetic MC-LF were identical to those of an authentic sample of the natural product.

24 thyl sulfides were proven by comparison with authentic samples of 2a-f, thus eliminating one of two p

25 culations (B3LYP/LanL2DZ) and comparisons to authentic samples of PIDA have confirmed the data analys

26 ansformation studies were also undertaken on authentic samples of two of the identified photoproducts

27 ied by GC and GC-mass spectral comparison to authentic samples produced independently; in some cases,

28 e same compounds; however, without access to authentic samples this cannot be unequivocally proven.

29 hesized using this approach are identical to authentic samples when tested by a variety of analytical

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