Pasireotide
A broader-spectrum somatostatin analog hitting more receptor subtypes.
Identity
- Class
- Somatostatin analog (cyclic hexapeptide)
- Source
- Synthetic analog of somatostatin
- Receptor
- Somatostatin receptors (SSTR1, 2, 3, and 5)
Key properties
Molecular weight
~1,047.2 Da
Approximate values for the native hormone. Engineered analogs are often deliberately larger and far longer-acting.
Mechanism
Pasireotide binds a wider range of somatostatin receptor subtypes than octreotide — including SSTR1, 2, 3, and 5 — giving it a different activity profile, notably more SSTR5 engagement that underlies its use in conditions octreotide addresses less well.
Reference notes
- Its broader SSTR-subtype coverage is the key distinction from octreotide and lanreotide.
- Greater SSTR5 affinity drives a different clinical profile.
- Illustrates how analog receptor-selectivity engineering changes effects.
Selected literature
Curated peer-reviewed reviews, sourced from PubMed. Selected for relevance, not exhaustive — open any entry on PubMed for the full record and its primary citations.
- 1.Diagnosis and Treatment of Pituitary Adenomas: A Review · JAMA, 2017 · PMID 28170483
- 2.Acromegaly · Nature reviews. Disease primers, 2019 · PMID 30899019