Receptor studies with novel insulin analogues and photoaffinity labelling techniques

2006 ◽  
pp. 223-225
Author(s):  
D. Brandenburg ◽  
M. Fabry ◽  
Y. Fischer ◽  
H. -G. Gattner ◽  
J. Grötzinger ◽  
...  
Keyword(s):  
Insulin Analogues ◽  
Photoaffinity Labelling

Are fast insulin analogues fast enough? Switching to faster aspart may reduce glycemic variability and the risk of hypoglycemia in type 1 diabetic patients on sensor-augmented insulin pump therapy

2019 ◽  
Author(s):  
Manuel Esteban Nivelo-Rivadeneira ◽  
Agnieszka Kuzior ◽  
Paula Maria Fernandez-Trujillo-Comenge ◽  
Ana Delia Santana-Suarez ◽  
Carmen Acosta-Calero ◽  
...  
Keyword(s):  
Insulin Pump ◽  
Glycemic Variability ◽  
Insulin Analogues ◽  
Insulin Pump Therapy ◽  
Diabetic Patients ◽  
Pump Therapy ◽  
Type 1 Diabetic Patients ◽  
Fast Insulin

Receptor binding and tyrosine kinase activation by insulin analogues with extreme affinities studied in human hepatoma HepG2 cells

Diabetes ◽  
1991 ◽  
Vol 40 (11) ◽  
pp. 1488-1495 ◽  
Author(s):  
K. Drejer ◽  
V. Kruse ◽  
U. D. Larsen ◽  
P. Hougaard ◽  
S. Bjorn ◽  
...  
Keyword(s):  
Tyrosine Kinase ◽  
Receptor Binding ◽  
Hepg2 Cells ◽  
Insulin Analogues ◽  
Human Hepatoma ◽  
Kinase Activation ◽  
Human Hepatoma Hepg2 Cells ◽  
Hepatoma Hepg2

Scintigraphic studies in rats. Kinetics of insulin analogues covering wide range of receptor affinities

Diabetes ◽  
1991 ◽  
Vol 40 (5) ◽  
pp. 628-632 ◽  
Author(s):  
I. Jensen ◽  
V. Kruse ◽  
U. D. Larsen
Keyword(s):  
Insulin Analogues ◽  
Wide Range ◽  
Kinetics Of

Ultra-Fast Acting Insulin Analogues

2014 ◽  
Vol 8 (2) ◽  
pp. 117-123 ◽  
Author(s):  
Sanjay Kalra ◽  
Yashdeep Gupta
Keyword(s):  
Insulin Analogues ◽  
Acting Insulin ◽  
Fast Acting

Photoreaction of N-butyl 3,4-dimethoxy-6-nitrobenzamide with butylamine. A model study for lysine-directed photoaffinity labelling

1987 ◽  
Vol 52 (7) ◽  
pp. 1780-1785 ◽  
Author(s):  
Petr Kuzmič ◽  
Libuše Pavlíčková ◽  
Milan Souček
Keyword(s):  
Nitro Group ◽  
Aromatic Ring ◽  
Ultraviolet Irradiation ◽  
Title Compound ◽  
Reductive Coupling ◽  
Photoaffinity Labelling ◽  
Photolysis Rate ◽  
Model Study ◽  
A Minor

Ultraviolet irradiation of the title compound I in the presence of butylamine gave predominantly products of nucleophilic photosubstitution by the amine, i.e., nitroanilines IIa and IIb. Besides, small amounts of products of hydrolysis (phenol III) and reductive coupling (azoxybenzene IV) were also formed. Comparison of the overall photolysis rate of I with that of 3,4-dimethoxy-1-nitrobenzene (V) indicates a minor loss of reactivity, most probably due to some deviation from coplanarity of the activating nitro group and the aromatic ring.

Current utilisation patterns for long-acting insulin analogues including biosimilars among selected Asian countries and the implications for the future

2021 ◽  
pp. 1-1
Author(s):  
Brian Godman ◽  
Mainul Haque ◽  
Santosh Kumar ◽  
Salequl Islam ◽  
Jaykaran Charan ◽  
...  
Keyword(s):  
Insulin Analogues ◽  
Asian Countries ◽  
Acting Insulin ◽  
The Future ◽  
Long Acting

Engineering of Orally Available, Ultralong-Acting Insulin Analogues: Discovery of OI338 and OI320

2020 ◽  
Author(s):  
Thomas B. Kjeldsen ◽  
František Hubálek ◽  
Tina M. Tagmose ◽  
Lone Pridal ◽  
Hanne H. F. Refsgaard ◽  
...  
Keyword(s):  
Insulin Analogues ◽  
Acting Insulin

scholarly journals A photoaffinity labelling study of the messenger RNA-binding region of Escherichia coli ribosomes

1978 ◽  
Vol 5 (9) ◽  
pp. 3389-3408 ◽  
Author(s):  
Harry Towbin ◽  
David Elson
Keyword(s):  
Escherichia Coli ◽  
Messenger Rna ◽  
Rna Binding ◽  
Binding Region ◽  
Photoaffinity Labelling
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