Type 1 Diabetes Complications 2011
DOI: 10.5772/24754
|View full text |Cite
|
Sign up to set email alerts
|

Hypoglycemia as a Pathological Result in Medical Praxis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2021
2021
2021
2021

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 75 publications
(63 reference statements)
0
1
0
Order By: Relevance
“…It was shown that the 3'-hydroxyl and 4'-hydroxyl group in the Ring B of the structure of a flavonoid, as well as the 3-hydroxyl residue in ring C, are very important for the inhibition of thrombin activity [51]. Ring B and C in flavonoids can interact with thrombin anchor S1 and S2, while ring A only partially interacts with S3 [64]. This suggests that the 3'-hydroxyl group and the 4'-hydroxyl group on the B ring of a flavonoid form hydrogen bond with amino acids to form the S1 anchor, which means that the B ring with hydroxyl groups at the position of R1 and R2 can mimic the arginine residue in P1 of thrombin substrates [65].…”
Section: Effect Of Hydroethanolic Extract On Clotting Timesmentioning
confidence: 99%
“…It was shown that the 3'-hydroxyl and 4'-hydroxyl group in the Ring B of the structure of a flavonoid, as well as the 3-hydroxyl residue in ring C, are very important for the inhibition of thrombin activity [51]. Ring B and C in flavonoids can interact with thrombin anchor S1 and S2, while ring A only partially interacts with S3 [64]. This suggests that the 3'-hydroxyl group and the 4'-hydroxyl group on the B ring of a flavonoid form hydrogen bond with amino acids to form the S1 anchor, which means that the B ring with hydroxyl groups at the position of R1 and R2 can mimic the arginine residue in P1 of thrombin substrates [65].…”
Section: Effect Of Hydroethanolic Extract On Clotting Timesmentioning
confidence: 99%