In rats, ibutamoren at 10 mg/kg stimulated GH release with lower potency than compound 4b at 0.1 mg/kg.
In plain wordsIn rats, ibutamoren was less potent than compound 4b at stimulating natural growth hormone release.
- Peptide
- MK-677 (ibutamoren)
- Outcome
- DecreaseGH release potency
- Study
ratsn: not reported in source
- Comparator
- compound 4b
- Outcome group
- Growth hormone and IGF-1 · Endocrine and hormones
- Studied dose
- 10 mg/kg · oralAs given in this study (rats).
Source sentences
Starting from capromorelin, we designed, synthesized, and characterized a novel orally active GHSR-1a agonist, compound 4b (hGHSR-1a EC50 = 0.49 nM), which effectively stimulates endogenous GH release in rats at oral doses as low as 0.1 mg/kg─100-fold more potent than ibutamoren (10 mg/kg).