Protein / target

Somatostatin receptor type 2

SSTR2P30874Homo sapiensSwiss-Prot
Clinically validated
Therapeutic maturity
7
Approved medicines
30
Clinical trials
Small-molecule tractable
Druggability
Advanced Clinical

Protein at a glance

Biological role

Somatostatin receptor activity

Primary system

Nervous system

Strongest disease association

acromegaly

Clinical evidence · score 0.61

Therapeutic maturity

Clinically validated target

7 approved medicines against this target

Druggability

Small molecule

Open Targets tractability · Advanced Clinical

Clinical development

7 approved · 7 in clinical development

30 linked trials

Derived from structured UniProt, Open Targets and literature data on this page.

Protein profile

UniProt 2026_02

Canonical identity and biological annotation from UniProt.

Function

Receptor for somatostatin-14 and -28. This receptor is coupled via pertussis toxin sensitive G proteins to inhibition of adenylyl cyclase. In addition it stimulates phosphotyrosine phosphatase and PLC via pertussis toxin insensitive as well as sensitive G proteins. Inhibits calcium entry by suppressing voltage-dependent calcium channels. Acts as the functionally dominant somatostatin receptor in pancreatic alpha- and beta-cells where it mediates the inhibitory effect of somatostatin-14 on hormone secretion. Inhibits cell growth through enhancement of MAPK1 and MAPK2 phosphorylation and subsequent up-regulation of CDKN1B. Stimulates neuronal migration and axon outgrowth and may participate in neuron development and maturation during brain development. Mediates negative regulation of insulin receptor signaling through PTPN6. Inactivates SSTR3 receptor function following heterodimerization

Subcellular location

Cell membraneCytoplasm
Domains and Gene Ontology detail (11)

Gene Ontology

  • Ccytosol
  • Cneuron projection
  • Cplasma membrane
  • Fneuropeptide binding
  • FPDZ domain binding
  • Fsomatostatin receptor activity
  • Pcellular response to estradiol stimulus
  • Pcellular response to glucocorticoid stimulus
  • PG protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
  • Pnegative regulation of cell population proliferation
  • Pneuropeptide signaling pathway

369 aa · 41 kDa · 2 isoforms

Biological roles

Reactome v97

What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.

G protein-coupled signallingGOKinase signallingUniProt
View supporting evidence

G protein-coupled signalling

  • ·G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messen…

Kinase signalling

  • ·Receptor for somatostatin-14 and -28. This receptor is coupled via pertussis toxin sensi…
View underlying pathways (2)

Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.

Interaction neighbourhood

STRING v12.0

Proteins with the strongest functional or physical association. Node size and line weight reflect STRING confidence; hover or select a partner to inspect one association.

SSTGNAI1GNAI3CORTGNAI2GNASGNB1DRD2GNG2GHRLSSTR2

10 strongest partners — larger node and heavier line mean higher confidence

Functional and physical associations from STRING v12.0. Only associations with this protein are drawn — partner-to-partner links are not part of this evidence.

Drugs targeting this protein

1

Whether each drug engages this protein directly or through a complex, and how many other targets are recorded for it. Direct binders with few recorded targets are listed first.

Somatostatin receptor binding agent

Acts on a complex — shared with SSTR5, SSTR4, SSTR1 +1 more · 1 of 5 recorded protein targets

ChEMBL mechanism, action type and target identity. Open Targets clinical status and indications.

Translational evidence

Open Targets 26

Why this target matters therapeutically — disease associations, drugs in development, tractability and safety, from Open Targets.

Highest-confidence therapeutic associations

Diseases where a drug acting on this target has already reached clinical development.

acromegaly0.99

Clinical · overall 0.61

neuroendocrine neoplasm0.94

Clinical · overall 0.59

neoplasm0.89

Clinical · overall 0.57

carcinoid tumor0.85

Clinical · overall 0.52

carcinoid syndrome0.82

Clinical · overall 0.50

Highest overall evidence

Remaining associations by Open Targets' aggregated evidence score.

ACTH-dependent Cushing syndrome0.48

Clinical

neuroendocrine carcinoma0.46

Clinical

cancer0.42

Literature

digestive system neuroendocrine tumor, grade 1/20.41

Clinical

hepatocellular carcinoma0.39

Literature

Show all associations
acromegaly0.61
neuroendocrine neoplasm0.59
neoplasm0.57
carcinoid tumor0.52
carcinoid syndrome0.50
ACTH-dependent Cushing syndrome0.48
neuroendocrine carcinoma0.46
cancer0.42
digestive system neuroendocrine tumor, grade 1/20.41
hepatocellular carcinoma0.39

Open Targets ranks 1,327 associations for this target and we store the top 10 by aggregated score. The long tail is largely literature co-mention and RNA-expression evidence, not evidence that this target drives those diseases.

Known drugs · 14 total

OCTREOTIDE ACETATEApproval

carcinoid tumor · cancer · acromegaly

LANREOTIDE ACETATEApproval

acromegaly · carcinoid syndrome

VELDOREOTIDEPhase 2

acromegaly · breast cancer

PASIREOTIDEApproval

acromegaly · ACTH-dependent Cushing syndrome · ACTH-dependent Cushing syndrome

LUTETIUM OXODOTREOTIDEPhase 3

digestive system neuroendocrine tumor, grade 1/2 · neuroendocrine neoplasm · pheochromocytoma

VAPREOTIDEPhase 3
PALTUSOTINEApproval

acromegaly · carcinoid syndrome · neuroendocrine neoplasm

OCTREOTIDEApproval

acromegaly · diabetic retinopathy · neuroendocrine neoplasm

SOMATOSTATINPhase 3

autosomal dominant polycystic kidney disease · gallbladder carcinoma · thymoma

PASIREOTIDE PAMOATEApproval

acromegaly

Tractability

SM · Advanced ClinicalSM · Structure with LigandSM · High-Quality LigandSM · Druggable FamilyAB · GO CC high confAB · UniProt loc med confAB · UniProt SigP or TMHMMPR · Small Molecule BinderOC · Approved Drug

Clinical trials

30

Trials of drugs that target this protein — reached indirectly through those drugs, so a trial listed here studies the drug, not the protein.

Show remaining trials (24)

RECRUITING · via lutetium Lu 177 dotatate · NCT04529044

RECRUITING · via lutetium Lu 177 dotatate · NCT06326190

COMPLETED · via lutetium Lu 177 dotatate · NCT06122610

ClinicalTrials.gov via the drug-target graph.

Forefront confidence

Synthesis

Our own weighting of the evidence behind each disease association. Human genetics and clinical evidence count for most; literature co-mention counts for little, because two entities sharing an abstract is not evidence that one drives the other.

acromegalyWell supported
0.75
agreement 0.600.91
Clinical95%Literature5%

Open Targets aggregate 0.61 · 2 independent evidence families

neuroendocrine neoplasmModerately supported
0.73
agreement 0.580.89
Clinical87%Literature13%

Open Targets aggregate 0.59 · 2 independent evidence families

neoplasmModerately supported
0.71
agreement 0.560.87
Clinical83%Literature17%

Open Targets aggregate 0.57 · 2 independent evidence families

carcinoid tumorModerately supported
0.65
agreement 0.490.80
Clinical96%Literature4%

Open Targets aggregate 0.52 · 2 independent evidence families

carcinoid syndromeModerately supported
0.61
agreement 0.460.77
Clinical99%Literature1%

Open Targets aggregate 0.50 · 2 independent evidence families

The evidence agreement range shows how closely the independent evidence families agree — it is not a statistical confidence interval, and nothing here is fitted to outcome data. Derived from Open Targets evidence types under Forefront weighting; the underlying per-type scores are shown above so the calculation can be checked.

What's happening now

2

Recent activity around this target, drawn from one canonical event stream. Every item is reached through a drug that targets this protein, so each event is news about that drug rather than about the protein directly.

  1. Regulatory approval2017-09-26

    Approval: Lutathera (EMA)

    ema · regulatory · ema · via lutetium Lu 177 dotatate

  2. New publication2008-05-01
    Treatment with the radiolabeled somatostatin analog [177 Lu-DOTA 0,Tyr3]octreotate: toxicity, efficacy, and survival.

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2008 · 1,022 citations · Europe PMC · via lutetium Lu 177 dotatate

Objective event titles are shown unmodified; the event kind and significance line are derived from structured fields. Forefront AttentionEvent stream aggregating Europe PMC Regulatory filings ClinicalTrials.gov.