Brief introduction of 20980-22-7

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The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 20980-22-7, Name is 2-(Piperazin-1-yl)pyrimidine, SMILES is C1(N2CCNCC2)=NC=CC=N1, in an article , author is Mohan, Gundluru, once mentioned of 20980-22-7, Computed Properties of C8H12N4.

Excellency of pyrimidinyl moieties containing alpha-aminophosphonates over benzthiazolyl moieties for thermal and structural stability of stem bromelain

An efficient approach has been made for the synthesis of a series of novel di alpha-aminophosphonates by the reaction of terephthalaldehyde with various pyrimidine/benzthiazole amines and diethyl phosphite using sulfonated graphitic carbon nitride – SA@g-C3N4 as catalyst under room temperature and solvent free conditions. Later, the different effects of these newly synthesized alpha-aminophosphonates as a function of concentration gradient has been scrutinized on the thermal and structural stability of stem bromelain (SBM) through combining the results of various spectroscopic techniques like UV-vis, steady state fluorescence and circular dichroism(CD). Lastly the competitive and distinctive behaviour of alpha-aminophosphonates towards the stability of SBM has been envisaged using molecular docking simulations which suggest that nature of alpha-aminophosphonates plays a crucial role for their interactions with SBM. Molecular docking results clearly show that alpha-aminophosphonates with pyrimidine ring are having more number of hydrogen bonding interaction with amino acid residues of SBM than alpha-aminophosphonates with benzthiazolyl ring. Sequentially for thermal and structure stability of SBM, concentration of alpha-aminophosphonates plays an inexorable role and through these results it must be concluded that most of the alpha-aminophosphonates are stabilizing the SBM upto the 0.1 mM concentration. (C) 2020 Elsevier B.V. All rights reserved.

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Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia