Novel fatty acid chain modified GLP-1 derivatives with prolonged in vivo glucose-lowering ability and balanced glucoregulatory activity.
Bioorg Med Chem · 2018
Last updated 2026-05-28Researchers modified two versions of a GLP-1 hormone (Cys-Gly-GLP-1(7-36)-NH and Cys-Gly-GLP-1(7-37)-NH) by attaching fatty acid chains to help them last longer in the body. One version, called I-6, showed the strongest ability to lower blood sugar in tests. When given once daily to diabetic mice, I-6 improved blood sugar control, reduced body weight, and had positive effects on blood chemistry over time.
AI summary of the abstract below.
| Journal | Bioorg Med Chem, 2018 |
|---|---|
| Citations | 10 |
| Relative citation ratio | 0.44 |
| NIH percentile | 26 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes |
Abstract
Glucagon-like peptide-1 is a potent hypoglycemic hormone with beneficial properties for the treatment of diabetes. However, its half-life is short because the rapid metabolic degradation. This study aims to prolong the half-life of glucagon-like peptide-1 through conjugation with the fatty acid side chain which helps the conjugates to interact with the albumin. Firstly, we chose two optimized polypeptide chains which have tremendous hypoglycemic effect named Cys-Gly-GLP-1(7-36)-NH and Cys-Gly-GLP-1(7-37)-NH, and various fatty acid chains were modified. All conjugates preserved relatively strong GLP-1R activation and I-6 behaved best in glucose-lowering ability. The prolonged antidiabetic effects of I-6 were further confirmed by hypoglycemic efficacy test in vivo. Meanwhile, once daily injection of I-6 to diabetic mice achieved long-term beneficial effects on glucose tolerance, body weight and blood chemistry. It is concluded that I-6 is a promising agent for further investigation of its potential to treat obese patients with diabetes.
Verbatim abstract via PubMed 29673717 ↗