Abstract
Appropriate N-terminus modification can result in somatostatin (SRIF) octapeptide analogs that are both more potent and more selective in vitro for the human SRIF receptor type 2 (hsst2). In addition, these modifications can improve the duration of action and bioavailability of SRIF analogs following parenteral administration, as shown by both pharmacological and distribution studies in vivo with BIM-23190 and BIM-23197 in the rat.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 24-26 |
| Number of pages | 3 |
| Journal | Metabolism: Clinical and Experimental |
| Volume | 45 |
| Issue number | SUPPL.1 |
| DOIs | |
| State | Published - 1996 |
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism
- Endocrinology