A Straightforward Synthesis and Structure–Activity Relationship of Highly Efficient Initiators for Two-Photon Polymerization

2013 ◽  
Vol 46 (2) ◽  
pp. 352-361 ◽  
Author(s):  
Zhiquan Li ◽  
Niklas Pucher ◽  
Klaus Cicha ◽  
Jan Torgersen ◽  
Samuel C. Ligon ◽  
...  
Keyword(s):  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Two Photon ◽  
Highly Efficient ◽  
Structure Activity ◽  
Relationship Of ◽  
Two Photon Polymerization

scholarly journals Synthesis and structure-activity relationship of several aromatic ketone-based two-photon initiators

2011 ◽  
Vol 49 (17) ◽  
pp. 3688-3699 ◽  
Author(s):  
Zhiquan Li ◽  
Marton Siklos ◽  
Niklas Pucher ◽  
Klaus Cicha ◽  
Aliasghar Ajami ◽  
...  
Keyword(s):  
Structure Activity Relationship ◽  
Aromatic Ketone ◽  
Activity Relationship ◽  
Two Photon ◽  
Structure Activity ◽  
Relationship Of

Silyl-based initiators for two-photon polymerization: from facile synthesis to quantitative structure–activity relationship analysis

2017 ◽  
Vol 8 (43) ◽  
pp. 6644-6653 ◽  
Author(s):  
Zhiquan Li ◽  
Arnulf Rosspeintner ◽  
Peng Hu ◽  
Guigang Zhu ◽  
Yuansheng Hu ◽  
...  
Keyword(s):  
Quantitative Structure Activity Relationship ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Quantitative Structure ◽  
Facile Synthesis ◽  
Two Photon ◽  
Relationship Analysis ◽  
Structure Activity ◽  
Stilbene Derivatives ◽  
Two Photon Polymerization

Silyl-based stilbene derivatives were straightforwardly prepared and successfully applied in two photon lithography as photoinitiators.

Structure-activity relationship of (-) mammea A/BB derivatives against Leishmania amazonensis

Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
MA Brenzan ◽  
CV Nakamura ◽  
BPD Filho ◽  
T Ueda-Nakamura ◽  
MCM Young ◽  
...  
Keyword(s):  
Structure Activity Relationship ◽  
Leishmania Amazonensis ◽  
Activity Relationship ◽  
Structure Activity ◽  
Relationship Of

Antineoplastic Activity, Structural Modification, Synthesis and Structure-activity Relationship of Dammarane-type Ginsenosides: An Overview

2019 ◽  
Vol 23 (5) ◽  
pp. 503-516 ◽  
Author(s):  
Qiang Zhang ◽  
Xude Wang ◽  
Liyan Lv ◽  
Guangyue Su ◽  
Yuqing Zhao
Keyword(s):  
Structural Modification ◽  
Gastrointestinal Disease ◽  
Structure Activity Relationship ◽  
Cerebrovascular Diseases ◽  
Activity Relationship ◽  
Cycle Arrest ◽  
Structure Activity ◽  
Wide Range ◽  
Structural Association ◽  
Relationship Of

Dammarane-type ginsenosides are a class of tetracyclic triterpenoids with the same dammarane skeleton. These compounds have a wide range of pharmaceutical applications for neoplasms, diabetes mellitus and other metabolic syndromes, hyperlipidemia, cardiovascular and cerebrovascular diseases, aging, neurodegenerative disease, bone disease, liver disease, kidney disease, gastrointestinal disease and other conditions. In order to develop new antineoplastic drugs, it is necessary to improve the bioactivity, solubility and bioavailability, and illuminate the mechanism of action of these compounds. A large number of ginsenosides and their derivatives have been separated from certain herbs or synthesized, and tested in various experiments, such as anti-proliferation, induction of apoptosis, cell cycle arrest and cancer-involved signaling pathways. In this review, we have summarized the progress in structural modification, shed light on the structure-activity relationship (SAR), and offered insights into biosynthesis-structural association. This review is expected to provide a preliminary guide for the modification and synthesis of ginsenosides.

Design, Facile Synthesis, Antibacterial Activity and Structure-Activity Relationship of Novel Di- and Tri-Substituted 1,3,5-Triazines

2012 ◽  
Vol 9 (3) ◽  
pp. 329-335 ◽  
Author(s):  
Surajit Kumar Ghosh ◽  
Ashmita Saha ◽  
Bornali Hazarika ◽  
Udaya Pratap Singh ◽  
Hans Raj Bhat ◽  
...  
Keyword(s):  
Antibacterial Activity ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Facile Synthesis ◽  
Structure Activity ◽  
Relationship Of
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