ライフサイエンスコーパス: sulfonation

1 aries are greatly dependent on the degree of sulfonation.

2 nd C(537) are involved in OONO(-)-mediated S-sulfonation.

3 ration during subsequent sample handling and sulfonation.

4 n may also be catalytically important in the sulfonation.

5 rol: The title reaction is effective for the sulfonation and alkylation of arenes bearing directing g

6 expressionof C53A DJ-1 enhanced both Cys-106 sulfonation and cell death.

7 ferase (EST), the enzyme responsible for the sulfonation and inactivation of estrogens, plays an impo

8 S-Sulfonation and S-cysteinylation are prevalent TTR modif

9 teinylation, glycosylation, fragmentation, S-sulfonation, and 3-chlorotyrosine formation.

10 tion, formylation, carboxylation, nitration, sulfonation, and others are discussed in detail, particu

11 O2 also induce cell death, with DJ-1 Cys-106 sulfonation appearing causal in these events, as express

12 y important PTMs such as phosphorylation and sulfonation, are difficult to multiply charge in positiv

13 ined with another derivatization, N-terminal sulfonation, as evidenced by tandem mass spectrometry (M

14 Upon sulfonation, carcinogenic hydroxyarylamines such as N-hy

15 Sulfonation conditions were developed for several BODIPY

16 subjected to regioselective deprotection and sulfonation conditions, which were optimized with the ai

17 Co-derivatization with N-terminal sulfonation confirmed the identity of low-abundance prot

18 Sulfonation controls the affinities of ligands for their

19 (410-427) and to evaluate the requirement of sulfonation for effective thrombin interaction.

20 vation, doping of heteroatoms, halogenation, sulfonation, grafting, polymer coating, noncovalent func

21 dditional information obtained by N-terminal sulfonation in combination with IRMPD provided significa

22 o be possible to accurately predict Phase II sulfonation in silico.

23 DJ-1 Cys-106 hyperoxidation (sulfination or sulfonation) in myocytes, perfused heart, or HEK cells.

24 method for localizing peptide and protein O-sulfonation involves derivatization of nonsulfonated tyr

25 Sulfonation is an important pathway in the biotransforma

26 Sulfonation is prized for its ability to impart water-so

27 lowing steps: chemical N-deacetylation and N-sulfonation leading to N-sulfoheparosan (-GlcA(1,4)GlcNS

28 S(1,4)GlcNS6S-); and selective enzymatic 3-O-sulfonation leading to the anticoagulant heparin, contai

29 heparin (-IdoA2S(1,4)GlcNS-); enzymatic 6-O-sulfonation leading to the heparin backbone (-IdoA2S(1,4

30 nditions where 5mC is resistant to analogous sulfonation leading to thymine (T).

31 ); enzyme-catalyzed C5-epimerization and 2-O-sulfonation leading to undersulfated heparin (-IdoA2S(1,

32 ansferase (PST) preferentially catalyzes the sulfonation of "simple" planar phenols, and levels of ac

33 Sulfonation of 5 and 6 with concentrated sulfuric acid a

34 ere prepared as the tetrasodium salts by the sulfonation of 5,10,15, 20-tetraphenyl-21,23-dithiaporph

35 ndrosterone sulfotransferase (Std) catalyzes sulfonation of androgenic steroids and certain aromatic

36 The human SULTs catalyzed the sulfonation of benzo[a]pyrene-7,8-catechol and generated

37 Sulfotransferase sulfonation of beta-hydroxy-acyl-ACP is followed by TE h

38 o quantitatively convert C to uracil (U) via sulfonation of denatured, single-stranded gDNA under con

39 otein ubiquitination based on the N-terminal sulfonation of diglycine branched peptides.

40 The 3-O-sulfonation of glucosamine residues in heparan sulfate (

41 Sulfonation of graphitic carbon nitride (g-CN) affords a

42 transferase is primarily responsible for the sulfonation of N-OH-2AAF in rat liver.

43 We investigated whether sulfonation of PAH catechols by human sulfotransferases

44 Different degrees of sulfonation of polyphenylenesulfone (PPSU) were adopted

45 Moreover, a selective ST-mediated sulfonation of the (R)-beta-hydroxyl group was found to

46 TAM adducts are primarily formed via sulfonation of the alpha-hydroxylated TAM metabolites.

47 Androgen inactivation via sulfonation of the hormone by dehydroepiandrosterone sul

48 ty due to mutation or prior oxidation (e.g., sulfonation) of the critical cysteine thiol, could thus

49 It has been established that the degree of sulfonation plays a role in both creating a macrovoid-fr

50 -5 '-phosphosulfate, the cosubstrate for the sulfonation reaction.

51 The sulfonation reagent Alexa Fluor 350 (AF350) provided the

52 s controlled by the sulfonation time and the sulfonation solution composition and can be as high as 3

53 We determined that S-sulfonation stabilized TTR tetramer stability by a facto

54 Upon sulfonation, SULT2A1 substrates become polar and water-s

55 Following sulfonation, the capillaries were coated with 65-nm-diam

56 n of the water dip varies with the degree of sulfonation; the elution order is normal (water dip appe

57 ation exchange capacity is controlled by the sulfonation time and the sulfonation solution compositio

58 Chemical derivatization by N-terminal sulfonation was carried out on several model peptides fo

59 De(acetylation), glucosylation and sulfonation were the main metabolic pathways activated.

60 mmodate sites of phosphorylation in place of sulfonation without sacrificing binding affinity.