ライフサイエンスコーパス: acridinium

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1 hydrolysis profiles and reduced affinity for acridinium affinity resin.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

18 Chemiluminescent acridinium ester labels are widely used in clinical diag

19 lution hybridization with a chemiluminescent acridinium ester oligonucleotide probe.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 A novel acridinium sensitizer provides enhanced reactivity withi

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

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