ライフサイエンスコーパス: bulkiness

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1 meso substituents of a controlled degree of bulkiness.

2 maintaining minimal perturbations in steric bulkiness and overall polarity of the triphosphate polya

3 icity, hydrophilicity, volume, surface area, bulkiness and refractivity.

4 on has not been developed yet because of the bulkiness and rigidity of conventional imaging modules a

5 The 2-Se atom bulkiness and the electronic effect are probably the mai

6 The results show that the bulkiness and the reactivity of this doubly activated in

7 such as substrate conformation, nucleophile bulkiness, and remote steric features can affect stereos

8 nic interactions (n --> pi*) and side chains bulkiness in promoting cis-amides was essentially invest

9 ketone peptide analogues with varying steric bulkiness in the P1 position and tested the ability of t

10 e supramolecular receptor not only with the "bulkiness" necessary for the NMR chemosensing approach b

11 n loss of PARG inhibition and the length and bulkiness of 8-adenosyl substituents was shown.

12 lored the possibility that by increasing the bulkiness of acrolein-adducted proteins, adduct-trapping

13 The bulkiness of amino acid residues in the C-terminal third

14 orded different products which depend on the bulkiness of aryl substituents.

15 PLM partially suffers from the high-cost and bulkiness of conventional lens-based microscopy, and its

16 dues this coupling is fostered by decreasing bulkiness of hydrophobic side chains due to larger hydra

17 h more sensitive toward the increased steric bulkiness of inhibitors compared to influenza A neuramin

18 nto the K+ channel Kv1.4, and found that the bulkiness of residues in the inactivation peptide is ess

19 phenols were investigated in relation to the bulkiness of substituents at the 2 and 6 positions of th

20 interactions become less important when the bulkiness of the alkyl groups attached to boron increase

21 ion of the substrate entry pore size and the bulkiness of the gating residues.

22 ntered on the isopropyl carbon in 2b and the bulkiness of the isopropyl group prevent the necessary r

23 aromaticity of the ligand and less so on the bulkiness of the ligand.

24 tivity can be achieved by varying the steric bulkiness of the ligand.

25 The bulkiness of the N-(1-alkyl) substituent was found to (a

26 ylated clusters is observed depending on the bulkiness of the phosphine's alkyl substituents and on t

27 rbene intermediate, which is enhanced by the bulkiness of the R group.

28 steric effect is described as the sum of the bulkiness of the R1 and R2 groups (i.e., normal steric e

29 The nature of the metal and the bulkiness of the residues at the tetramic acid chelator

30 he nature of nucleophiles and (2) the steric bulkiness of the substituents at C-2 and C-4 of the cycl

31 droxide are largely influenced by the steric bulkiness of the substituents at C-2 and C-4 of the cycl

32 upon either migratory ability or the steric bulkiness of the substituents at C1 and C5.

33 or the diastereoselectivity with the greater bulkiness of the substituents giving higher diastereosel

34 lectivity of the reaction increased with the bulkiness of the substituents of the aldehyde donor in t

35 l substitutions resulting from the different bulkiness of the substituents were demonstrated by the X

36 arameters of PSII function in these mutants, bulkiness of the substituted amino acids is highly corre

37 However, the bulkiness of the W1 region implies that the DNA conforma

38 electivity among inorganic cations or on the bulkiness of their acidic side chains at the locus of se

39 aining patterns were created based upon the "bulkiness" of the individual amino acid side-chains in t

40 r reactions because the substituent's steric bulkiness raises the activation energy of the favored C-

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