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Octreotide

also known as Sandostatin

approved hormone endocrinegastrointestinal sequence not characterised
SSOOOOOOOOOONNNNNNNNNNHHHHHHHHHHHHHHH
71 heavy atoms · 141 bonds · drag to pan, scroll to zoom C49O10N10S2

Skeletal structure drawn from the computed atomic coordinates in PubChem CID 448601. Carbons are implicit vertices; hydrogens on carbon are suppressed, as in any structural formula. Nothing here is estimated — every atom sits where PubChem placed it.

Research reference only. The observations below are recorded in the cited literature. Nothing here is advice or a recommendation, and no dosing information is published on this site.

Sequence

Primary structure not characterised in the public records this index draws on. Nothing is shown rather than something invented.

D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr(ol) — a disulfide-cyclised octapeptide with D-residues and a C-terminal amino alcohol.

Molecular data

Chemical fields come from the PubChem compound record; computed values are derived from the sequence shown above.
molecular formulaC49H66N10O10S2
molecular weight1019.2 Da (PubChem)
computed backbone massnot characterised
lengthnot characterised
net charge (pH 7.4)not characterised
mean hydropathynot characterised
half-lifenot characterised
delivery routesubcutaneous, intramuscular
PubChem CID448601
PDBnot characterised
UniProt parentnot characterised

Mechanism

Somatostatin analogue with SSTR2/SSTR5 selectivity.

Reported targets: SSTR2 SSTR5

Experimental structure

No experimental structure of this peptide is deposited in the PDB. Nothing is rendered here — a predicted fold would not be a structure, and this site does not draw one.

Reported effects

Each row is an outcome described in the literature indexed for this peptide. Reported in the cited work — not a claim, not a recommendation.

Reported observations and the corpus they are drawn from.
reported outcomewhere it appears
GH suppressionAcromegaly Secondary to Ectopic Growth Hormone-Releasing Hormone Secretion F… Cureus 2026
acromegaly outcomes in trialsOctreotide and direct/indirect lung injury Research in pharmaceutical sciences 2025

Registered trials

Records from ClinicalTrials.gov. Listed for reference — this project sponsors no trial and is not involved in any of them.
NCTtitlestatusphase
NCT00113360RAD001 Plus Octreotide Depot in Metastatic or Unresectable Low Grade Neuroendocrine CarcinomCOMPLETEDPHASE2
NCT01137682Efficacy and Safety of Pasireotide Long Acting Release (LAR) Versus Octreotide LAR or LanreoCOMPLETEDPHASE3
NCT05361668Study to Evaluate the Safety, PK, and Dose Response of Paltusotine in Subjects With CarcinoiCOMPLETEDPHASE2
NCT00383708Lanreotide Autogel and Pegvisomant Combination Therapy in Acromegalic PatientsCOMPLETEDPHASE3
NCT00049023Radiolabeled Octreotide in Treating Children With Advanced or Refractory Solid TumorsCOMPLETEDPHASE1

Literature (8)

Acromegaly Secondary to Ectopic Growth Hormone-Releasing Hormone Secretion From Metastatic Bronchial Carcinoid Tumor: A Case Report — Cureus 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42571548 · DOI 10.7759/cureus.112355

Octreotide and direct/indirect lung injury — Research in pharmaceutical sciences 2025

Background and purposeLung injury is one of the most important diseases, which is accompanied by hypoxemia, organ failure, and a high mortality rate. There are several symptoms and causes of lung injuries. In the past years, special attention has been given to investigating the pathophysiology and the treatment of this disease. Octreotide, as an anti-inflammatory, anti-secretory, tissue-repairing, and anti-fibrotic drug, has been considered and administered for the treatment of lung injury. This review article considered the pharmacological effects of octreotide on physiopathological conditions in patients or animal models that have direct or indirect lung injury.Search strategy and findingsKeywords including "octreotide" OR "sandostatin" AND "lung injury" OR "ARDS" OR "respiratory distress" OR "lung fibrosis" were searched in the database of PubMed, and 44 articles were found. According…

open access ↗ · PMID 40933598 · DOI 10.4103/rps.rps_67_24

A Case Report: Fatal Mesenteric Microvascular Compromise Following Methamphetamine use and Insulin Overdose Treated with Octreotide — South Dakota medicine : the journal of the South Dakota State Medical Association 2025

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42470334

Long-Term Results of Long-Acting Somatostatin Analog Therapy in Children with Congenital Hyperinsulinism — Journal of clinical research in pediatric endocrinology 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42619456 · DOI 10.4274/jcrpe.galenos.2026.2026-3-12

Impact of Duration of Intravenous Octreotide Infusion on Achieving Hemostasis in Patients With Acute Variceal Hemorrhage — The Annals of pharmacotherapy 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42661447 · DOI 10.1177/10600280261478164

Octreotide as Adjunctive Therapy for Catecholamine-Secreting Pheochromocytoma and Paraganglioma — The Journal of clinical endocrinology and metabolism 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42626938 · DOI 10.1210/clinem/dgag343

Octreotide-assisted endoscopy versus octreotide-assisted TIPS for acute esophagogastric variceal bleeding with and without terlipressin intensification: A real-world study — Research Square 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · DOI 10.21203/rs.3.rs-10679798/v1

Combined SSTR2-targeted Analogue with <sup>177</sup>Lu-DOTATATE radionuclide and octreotide therapy for refractory meningioma: a case report — Frontiers in oncology 2026

Meningiomas are the most common primary intracranial tumor in adults. Beyond surgery and radiation, no standard of care therapy exists. Meningiomas overexpress somatostatin receptor 2 (SSTR2), providing the rationale for somatostatin analogue-based therapies, including octreotide. The addition of everolimus, a mammalian target of rapamycin inhibitor, to octreotide marginally improves the 6-month progression-free survival (PFS) rate. For this reason, novel therapies have emerged for the treatment of refractory meningiomas, including somatostatin receptor targeted radionuclide therapy. However, preliminary results with refractory meningiomas treated with single agent 177Lu-DOTATATE, a β-emitting peptide receptor radionuclide therapy (PRRT), demonstrated outcomes comparable to those observed with combination octreotide and everolimus. In contrast, in neuroendocrine tumors (NETs), octreotide…

open access ↗ · PMID 42370133 · DOI 10.3389/fonc.2026.1820428

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