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Vincent KA Tilley GJ Quammie NC Streeter I Burgess BK Cheesman MR Armstrong FA 《Chemical communications (Cambridge, England)》2003,(20):2590-2591
Addition of an equivalent of a polyaminocarboxylate ligand (L) to a solution of a redox protein and the aqua Eu2+ ion results in the instantaneous in situ generation of a very powerful reductant Eu(II)-L that can rapidly drive an electron stoichiometrically onto a redox centre having an extremely negative reduction potential (lower than -1 V): this is exemplified by straightforward generation of the super-reduced state of the Fe-protein of nitrogenase. 相似文献
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Duygu İNCİ 《应用有机金属化学》2020,34(12):e6016
NOO-type tridentate Schiff base, N-salicylidene-2-aminobenzoic acid, (H2L), and its ternary Cu (II) complex containing H2L Schiff base and 4,7-dimethyl-1,10-phenanthroline (4,7-dmphen), [Cu(4,7-dmphen)(H2L)]27H2O, have been synthesized and characterized by CHN analysis, ESI-MS, FTIR, and single-crystal X-ray diffraction techniques. The interaction of alone H2L Schiff base ligand and ternary Cu (II) complex with biomacramolecules {calf thymus DNA (CT-DNA) and bovine serum albumin (BSA)} has been investigated by electronic absorption and fluorescence spectroscopy. The experimental results indicate that H2L Schiff base ligand and ternary Cu (II) complex bind to CT-DNA by means of a moderate intercalation mode. Furthermore, the fluorescence quenching mechanism between H2L Schiff base ligand and ternary Cu (II) complex with BSA possesses a static quenching process. Radical scavenging activity of H2L Schiff base ligand and ternary Cu (II) complex was measured in terms of EC50, using the DPPH and H2O2 methods. Biomacromolecule interactions and scavenging activity studies revealed that ternary Cu (II) complex yielded better results than H2L Schiff base ligand alone. 相似文献
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Lawrence H.Lazarus 《中国化学快报》2011,22(8):907-910
Analogues of endomorphin and tripeptidcs modified at positions 4 and 3,respectively,with various phenylalanine analogues were synthesized and their affinities for opioid receptors were evaluated.Most of the peptides exhibited potentμ-receptor affinity and selectivity,among them,compound 7(Dmt-Pro-Tmp-Tmp-NH_2) exhibited potent affinity for bothμ-andδ-receptors (K_iμ= 0.47 nmol/L,K_iδ= 1.63 nmol/L). 相似文献
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Barrette J Bellwied R Braun-Munzinger P Cleland WE Cormier T Dadusc G David G Dee J Diebold GE Dietzsch O Duek E Fatyga M Fox D Greene SV Germani JV Hall JR Hemmick TK Herrmann N Hogue RW Hong B Jayananda K Kraus D Kumar BS Lacasse R Lissauer D Llope WJ Ludlam TW Majka R Makowiecki D Mark SK Mitchell JT Muthuswamy M O'Brien E Pruneau C Rotondo FS Sandweiss J da Silva NC Simon-Gillo J Slaughter J Sonnadara U Stachel J Takai H Takagui EM Throwe TG Waters L Winter C Wolf K Wolfe D Woody CL Xu N 《Physical review letters》1993,70(12):1763-1766
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