ライフサイエンスコーパス: acridinium

1 Moreover, the acridinium/acridane conversion leads to a significant ch

2 hydrolysis profiles and reduced affinity for acridinium affinity resin.

3 n demonstrated by use of resolvable N-linked acridinium and 2,7-dimethoxyacridinium ester labeled pro

4 ds, consisting of cationic trialkylammonium, acridinium, and tacrine ligands with tethers of varying

5 In sharp contrast, the acridinium-based biradicals, most with the radical sites

6 of the key radical intermediate state of an acridinium-based conPET catalyst and detailed investigat

7 -atom skeletal editing approach to construct acridinium-based crystalline COFs through an irreversibl

8 The structure of the stable acridinium-based radical photoproduct was unambiguously

9 catalysts is described based upon dicationic acridinium/carbene hybrids.

10 ion of H2O2 with 10-methyl-9-(p-formylphenyl)acridinium carboxylate trifluoromethanesulfonate and a m

11 oxylate, while the reaction is zero-order in acridinium catalyst, consistent with another finding sug

12 tionalize arenes that are not oxidized by an acridinium catalyst, such as benzene and toluene, thus s

13 sible by an oxidative (E*(red) = 2.15 V) N-H acridinium catalyst, which allowed for the functionaliza

14 ltrifluoroborates to nitriles via a Fukuzumi acridinium-catalyzed process.

15 ith a fluorinated pentacyclic quino[4,3,2-kl]acridinium cation (RHPS4).

16 ridin-9-ylamino)ethyl]-1,3-dimethylthiourea, acridinium cation, 1), the prototype of a new class of c

17 , and acridine orange (3,6-bis(dimethylamino)acridinium chloride), as well as 140 copies of therapeut

18 For the monochlorinated acridinium compound, a highly selective ring-closing rea

19 Although, chemiluminescence from acridinium compounds was discovered more than 50 years a

20 The methodology relies on the use of an acridinium dye to generate the boron-centered radicals f

21 A highly chemiluminescent reporter molecule, acridinium ester (AE), was tethered to single-stranded o

22 robes labeled with a highly chemiluminescent acridinium ester (AE).

23 robes labeled with a highly chemiluminescent acridinium ester (AE).

24 The acridinium ester 4-(2-succinimidyloxycarbonylethyl)pheny

25 tein conjugate that has been labeled with an acridinium ester as the chemiluminescent probe and secon

26 upon energy transfer (ET) from an in-common, acridinium ester chemiluminophore to a covalently conjug

27 Chemiluminescent acridinium ester labels are widely used in clinical diag

28 lution hybridization with a chemiluminescent acridinium ester oligonucleotide probe.

29 dan-9-carboxylate produces the corresponding acridinium ester, which reacts with hydrogen peroxide fo

30 an anti-human superoxide dismutase, dimethyl acridinium ester-labeled monoclonal antibody for detecti

31 e, transcription-mediated amplification, and acridinium ester-labeled probe chemistry on the automate

32 Chemiluminescence (CL) of acridinium esters (AE) has found widespread use in analy

33 h as hexa(ethylene)glycol to generate unique acridinium esters that are stable and are useful in impr

34 fficiency for the carboxylates to quench the acridinium excited state.

35 nt, converting the xanthylium precursor into acridinium frameworks.

36 kl]acridines and 8,13-dimethylquino[4,3,2-kl]acridinium iodides bearing bulky saturated (3-acetoxy)pr

37 Moreover, acridinium-labeling of AtRALF1 indicated that the bindin

38 ,4,5-tetra(4-aminophenyl)benzene (TADB) into acridinium-linked COFs, denoted as Acr-TAPB and Acr-TADB

39 ed as desired at the 3'-phenyl position with acridinium-mediated photoredox radiodeoxyfluorination in

40 -Difluoro-6,8,13-trimethyl-8H-quino[4,3,2-kl]acridinium methosulfate (12d, RHPS4, NSC 714187) has a h

41 (i) upon addition of nucleophiles converting acridinium moieties into the non-aromatic acridane deriv

42 ), and aryl diazonium salts engaging mesityl acridinium perchlorate as a photocatalyst.

43 eas di- and tri-C(sp(3))-H alkylation by the acridinium photocatalyst follows the SET mechanism.

44 osphoramides and thiophosphoramides using an acridinium photocatalyst is reported with good yield and

45 per catalytic turnover, while commonly used acridinium photocatalysts are not able to perform the ch

46 catalyst system is comprised of the Fukuzumi acridinium photooxidant (1) and a substoichiometric quan

47 edox-based catalyst system, consisting of an acridinium photooxidant and a nitroxyl radical, promotes

48 halofunctionalization through the use of an acridinium photooxidant in conjunction with a copper coc

49 no- and oxycyanation of olefins utilizing an acridinium photooxidant in conjunction with copper catal

50 The catalytic system consists of a Fukuzumi acridinium photooxidant with phenyldisulfide acting as a

51 es via direct C-H functionalization using an acridinium photoredox catalyst and trimethylsilyl cyanid

52 e oxidative and reductive capabilities of an acridinium photoredox catalyst to forge the densely func

53 nes, by direct C-H functionalization with an acridinium photoredox catalyst under an aerobic atmosphe

54 roducing the chlorine functionalities in the acridinium precursor, positions complementary to those p

55 ting methoxy groups at C-2 and/or C-7 in the acridinium ring with increased light output.

56 The pentacyclic acridinium salt RHPS4 displays anti-tumour properties in

57 rate that an air-stable photoredox catalyst (acridinium salt), together with a mild and air-stable re

58 f unactivated alkenes using CF(3)SO(2)Na and acridinium salt.

59 ensive series of quaternized quino[4,3,2- kl]acridinium salts against tumor cell lines in vitro have

60 Herein, we report a series of novel acridinium salts as alternatives to iridium photoredox c

61 nt o-(dimethylamino)aryl ketones, acridones, acridinium salts, and 1H-indazoles has been developed st

62 A novel acridinium sensitizer provides enhanced reactivity withi

63 well understood particularly in relation to acridinium structure and overall light output.

64 multi-responsive receptor consisting of two (acridinium-Zn(II) porphyrin) conjugates has been designe

65 Interestingly, for the bis(acridinium-Zn(II) porphyrin) receptor, charge-transfer l