TY - JOUR
T1 - Reverse docking, molecular docking, absorption, distribution, and toxicity prediction of artemisinin as an anti-diabetic candidate
AU - Ruswanto, Ruswanto
AU - Mardianingrum, Richa
AU - Siswandono, Siswandono
AU - Kesuma, Dini
N1 - Publisher Copyright:
© 2020, Universitas Jenderal Soedirman. All rights reserved.
PY - 2020/7
Y1 - 2020/7
N2 - Aldose reductase is an enzyme that catalyzes one of the steps in the sorbitol (polyol) pathway that is responsible for fructose formation from glucose. In diabetes, aldose reductase activity increases as the glucose concentration increases. The purpose of this research was to identify and develop the use of artemisinin as an anti-diabetic candidate through in silico studies, including reverse docking, receptor analysis, molecular docking, drug scan, absorption, and distributions and toxicity prediction of artemisinin. Based on the results, we conclude that artemisinin can be used as an anti-diabetic candidate through inhibition of aldose reductase.
AB - Aldose reductase is an enzyme that catalyzes one of the steps in the sorbitol (polyol) pathway that is responsible for fructose formation from glucose. In diabetes, aldose reductase activity increases as the glucose concentration increases. The purpose of this research was to identify and develop the use of artemisinin as an anti-diabetic candidate through in silico studies, including reverse docking, receptor analysis, molecular docking, drug scan, absorption, and distributions and toxicity prediction of artemisinin. Based on the results, we conclude that artemisinin can be used as an anti-diabetic candidate through inhibition of aldose reductase.
KW - Aldose reductase
KW - Artemisinin
KW - Molecular docking
KW - Reverse docking
UR - http://www.scopus.com/inward/record.url?scp=85090619951&partnerID=8YFLogxK
U2 - 10.20884/1.jm.2020.15.2.579
DO - 10.20884/1.jm.2020.15.2.579
M3 - Article
AN - SCOPUS:85090619951
SN - 1907-9761
VL - 15
SP - 88
EP - 96
JO - Molekul
JF - Molekul
IS - 2
ER -