ライフサイエンスコーパス: hydrogen donor

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1 hemistry, where an alcohol plays the role of hydrogen donor.

2 l conditions, but employing isopropanol as a hydrogen donor.

3 which the phenolic group could also serve as hydrogen donor.

4 onadiabatic tunneling, the dominant reactive hydrogen donor-acceptor distance (DAD) is typically ca.

5 is accompanied by the disruption of a single hydrogen donor-acceptor pair.

6 tors reveals that E(G) is centered about the hydrogen donor/acceptor ionization energy epsilon(+/-).

7 uch higher phenol content (2- to 7-fold) and hydrogen donor activity (1.5- to 4-fold) than widely con

8 H-transfer efficiency, the distance between hydrogen donor and acceptor is a very important factor.

9 ores that influence the distance between the hydrogen donor and acceptor.

10 en bonds, in which a carbon atom acts as the hydrogen donor and an electronegative atom Y (Y=N, O or

11 emperature using tri-n-butyltin hydride as a hydrogen donor and without the aide of a radical initiat

12 om a 1.28 A resolution structure, to contain hydrogen donors and acceptors that are satisfied by inte

13 e hydrogen bonding between the amine groups (hydrogen-donor) and the phosphate/carbonyl groups or wat

14 Using o-phenylenediamine (OPD) as a hydrogen donor (citrate-phosphate as pH buffer), the opt

15 of the T4 infection cycle and can serve as a hydrogen donor for the phage ribonucleotide reductase in

16 aredoxin 2 is shown to be the most effective hydrogen donor for the reduction of arsenate by ArsC.

17 itous redox proteins that were discovered as hydrogen donors for ribonucleotide reductase, the key en

18 Due to the increasing number of hydrogen-donors from DPPE molecules with increasing conc

19 Moreover, our simulations suggest that hydrogen donor functionalities close to the metabolic si

20 enzyme (APR1p) can use GSH efficiently as a hydrogen donor in vitro, showing aKm[GSH] approximately

21 tion of benzaldehydes using formate salts as hydrogen donors in aqueous isopropanol.

22 ducts of the alkyl-transfer reactions act as hydrogen donors in the presence of aromatic N-heterocycl

23 xplain why fluorescence quenching induced by hydrogen donors is less general for (1)(pi,pi*) than for

24 mixture of a decanoic acid ester precursor, hydrogen donor molecules, and a ruthenium-based photocat

25 Psi has two hydrogen donors (N1 and N3 imino protons) and two hydrog

26 , in animal cells, Trx may not be the direct hydrogen donor or that there may be a Trx-independent re

27 Only guests with two strong hydrogen donors, such as O-H bonds or amide N-H bonds, t

28 of reactions carried out in the presence of hydrogen donors supported the findings from DFT calculat

29 uction in which the NHC borane serves as the hydrogen donor, thus obviating the use of tin-based reag

30 sized 4'-hydroxy flavyliums were examined as hydrogen donors to DPPH, ABTS and hydroxyl radicals, and

31 er of these substrates, a huge excess of the hydrogen donor was not necessary.

32 The peroxidase activity of POD-A toward hydrogen donors was both pH- and concentration-dependent

33 general model for fluorescence quenching by hydrogen donors, where the radiationless decay occurs at

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