ライフサイエンスコーパス: amino nitrogen

1 sence or presence of a methyl group at the 4-amino nitrogen.

2 n active site potassium ion with the epsilon-amino nitrogen.

3 rance and suppress oxidation of BBT at the 1-amino nitrogen.

4 starch liquefaction time and increased free amino nitrogen.

5 ble nitrogen, viscosity, friability and free-amino nitrogen.

6 inding the oxazolidines together at their 3'-amino nitrogens.

7 ises from slow on-off proton exchange of the amino nitrogen, a process influenced by solution tempera

8 an index of collagen accumulation) and alpha-amino nitrogen (alpha-AN, mmol/cm, an index of total pro

9 In each polypeptide chain, the free alpha-amino nitrogen and carbonyl oxygen of the amino-terminal

10 nally, the internuclear distance between the amino nitrogens and the extent of modulation of basal [3

11 states from +5 (nitrate) to -3 (ammonium and amino-nitrogen), and its oxidation and reduction reactio

12 ltose, glucose, filterability, extract, free amino nitrogen, and fermentability.

13 bone amide nitrogen atoms and the N-terminal amino nitrogen atom in [OT - 3H + Cu](-).

14 ds were specifically labeled with 15N at the amino nitrogen atom.

15 Hg(II) with two thioether sulfur atoms, two amino nitrogen atoms, and a phenol oxygen atom arranged

16 utylsalicylidenimine) chelate built onto two amino nitrogens attached to the pz periphery; R is a sol

17 Fetal plasma glucose, lactate or alpha-amino nitrogen concentrations were unaffected by treatme

18 f reducing sugars, ethanol, acetic acid, and amino nitrogen did not differ significantly (p<0.05) bet

19 here interactions with the substrate's alpha-amino nitrogen differ between MarE and TDO, and the subs

20 The introduced epsilon-amino nitrogen in the C17K mutant occupies a significant

21 The introduced epsilon-amino nitrogen in the D206K mutant occupies a position i

22 ing their synthesis, a broad spectrum of the amino nitrogen is actively loaded into the phloem of lea

23 icyclo[3.2.1]octanes and demonstrate that an amino nitrogen is not required for binding to the DAT.

24 SAM and orient the lone pair orbital on the amino nitrogen (N) of Gly toward the donor methyl group

25 vy atom isotope effects at C-2, C-3, and the amino nitrogen of aspartate were determined for the reac

26 An (15)N R1rho NMR experiment targeting the amino nitrogen of guanine (dG-N2) provides direct eviden

27 he N(3) atom of histidine and the terminal e-amino nitrogen of lysine-occupy the same position and po

28 ase between C-4' of the PLP cofactor and the amino nitrogen of the sugar.

29 H92 to E91 to W412 to G413 pathway to the 4'-amino nitrogen of the thiamin diphosphate cofactor.

30 ity of ciprofloxacin by N-acetylation at the amino nitrogen on its piperazinyl substituent.

31 opy with selective 15N-labeling of exocyclic amino nitrogens on bases of interest, we are able to res

32 is always occupied, which may be either the amino nitrogen or the carboxy carbonyl oxygen.

33 r substrate by abstracting a H atom from the amino-nitrogen position.

34 The initial carbon to free amino nitrogen ratio of crude hydrolysates was optimised

35 We assign these to the imino and amino nitrogens, respectively, based on DFT calculations

36 d to assimilate the resulting peptides as an amino nitrogen source.

37 with secondary amino nitrogens than primary amino nitrogens tethered to the silica.

38 re found to form more readily with secondary amino nitrogens than primary amino nitrogens tethered to

39 The chemical shift of the amino nitrogen was deshielded by N1-methylation and then

40 e accessibility for formaldehyde of cytosine amino nitrogens within WC base pairs adjacent to HG base