Solution Behavior of IFN-β-1a: An Empirical Phase Diagram Based Approach

2005 ◽  
Vol 94 (9) ◽  
pp. 1893-1911 ◽  
Author(s):  
Haihong Fan ◽  
John Ralston ◽  
Mary Dibiase ◽  
Eric Faulkner ◽  
C. Russell Middaugh
Keyword(s):  
Phase Diagram ◽  
Solution Behavior ◽  
Empirical Phase Diagram

Stability of theClostridium botulinumType A Neurotoxin Complex:  An Empirical Phase Diagram Based Approach

2007 ◽  
Vol 4 (4) ◽  
pp. 571-582 ◽  
Author(s):  
Duane T. Brandau ◽  
Sangeeta B. Joshi ◽  
Aaron M. Smalter ◽  
Seonyoung Kim ◽  
Bryan Steadman ◽  
...  
Keyword(s):  
Phase Diagram ◽  
Empirical Phase Diagram ◽  
Neurotoxin Complex

A Molecular Dynamics Study of the Terminal Zr(Ni) Solid Solutions

1995 ◽  
Vol 400 ◽  
Author(s):  
F. Cleri ◽  
G. Mazzone ◽  
V. Rosato
Keyword(s):  
Molecular Dynamics ◽  
Phase Diagram ◽  
Solid Solutions ◽  
Tight Binding ◽  
Solid State Reactions ◽  
Binding Potential ◽  
Terminal Portion ◽  
Many Body ◽  
Empirical Phase Diagram ◽  
Dynamics Simulations

AbstractThe Zr terminal portion of the Zr-Ni phase diagram has been evaluated by means of a many-body tight-binding potential. The internal energy curves of the Zr(Ni) solid solutions at T=300 K have been calculated by Molecular Dynamics simulations. These curves exhibit positive values, contrary to former empirical phase diagram calculations. Implications of these results relevant to the problem of amorphization in metallic systems by solid-state reactions are discussed.

Water soluble palladium(ii) and platinum(ii) acyclic diaminocarbene complexes: solution behavior, DNA binding, and antiproliferative activity

2020 ◽  
Vol 44 (15) ◽  
pp. 5762-5773 ◽  
Author(s):  
Tatiyana V. Serebryanskaya ◽  
Mikhail A. Kinzhalov ◽  
Vladimir Bakulev ◽  
Georgii Alekseev ◽  
Anastasiya Andreeva ◽  
...  
Keyword(s):  
Dna Binding ◽  
Antiproliferative Activity ◽  
Water Soluble ◽  
Solution Behavior ◽  
Antitumor Potential ◽  
Acyclic Diaminocarbene

Water soluble Pd(ii) and Pt(ii)–ADC species synthesized via the metal-mediated coupling of isocyanides and 1,2-diaminobenzene have demonstrated antitumor potential.

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