Selenomethionine

drug
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Also known as NSC-760370SID50125779SID144206245

Summary

Selenomethionine (CHEMBL113178) is an approved small molecule; indicated across 8 conditions including colorectal adenocarcinoma and follicular lymphoma.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Indications: 8 conditions
  • Clinical trials: 11
  • Chemistry: 196.12 Da · C5H11NO2Se

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL113178
NameSelenomethionine
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID105024
ChEBICHEBI:30021
Molecular formulaC5H11NO2Se
Molecular weight196.12
InChIKeyRJFAYQIBOAGBLC-BYPYZUCNSA-N

SMILES: C[Se]CC[C@@H](C(=O)O)N

IUPAC name: (2S)-2-amino-4-methylselanylbutanoic acid

ChEBI definition: The L-enantiomer of selenomethionine.

Also known as: NSC-760370, Selenomethionine, SID50125779, SID144206245, SELENOMETHIONINE, selenomethionine

Parent form; salt/anhydrous children: CHEMBL1201054

Patent coverage: 5,947 distinct patent families (13,599 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: 4’-phosphopantetheinyl transferase ffp.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

8 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
colorectal adenocarcinoma2MONDO:0005008EFO:0000365
follicular lymphoma2MONDO:0018906MONDO:0018906
Hashimoto thyroiditis2MONDO:0007699EFO:0003779
lung neoplasm2MONDO:0021117MONDO:0008903
colorectal neoplasm2MONDO:0005335MONDO:0005575
clear cell renal carcinoma1MONDO:0005005EFO:0000349
colorectal adenoma1MONDO:0005484EFO:0005406

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 11.

Phase distribution

PhaseTrials
PHASE26
PHASE1/PHASE22
EARLY_PHASE11
PHASE11
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05363631PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSeleno-L Methionine (SLM)-Axitinib-Pembrolizumab
NCT00526890PHASE2TERMINATEDCarboplatin, Paclitaxel, Selenomethionine, and Radiation Therapy in Treating Patients With Stage III Non-Small Cell Lung Cancer That Cannot Be Removed by Surgery
NCT00625183PHASE2TERMINATEDCapecitabine, Oxaliplatin, Selenomethionine, and Radiation Therapy in Treating Patients Undergoing Surgery For Newly Diagnosed Stage II or III Rectal Adenocarcinoma
NCT00736164PHASE2WITHDRAWNSelenomethionine in Treating Patients Undergoing Surgery or Internal Radiation Therapy for Stage I or Stage II Prostate Cancer
NCT00736645PHASE2COMPLETEDSelenomethionine and Finasteride Before Surgery or Radiation Therapy in Treating Patients With Stage I or Stage II Prostate Cancer
NCT01682031PHASE2TERMINATEDSelenomethionine in Reducing Mucositis in Patients With Locally Advanced Head and Neck Cancer Who Are Receiving Cisplatin and Radiation Therapy
NCT02302768PHASE2UNKNOWNEffect of Semet (80 and 160 mcg) Versus Placebo in Euthyroid Patients With AIT
NCT02535533PHASE1/PHASE2COMPLETEDSLM + Axitinib for Clear Cell RCC
NCT04952129PHASE1COMPLETEDOptimal Selenium for Bowel Polyps (OSCAR)
NCT01211561EARLY_PHASE1UNKNOWNColon Cancer Prevention Using Selenium
NCT01112449Not specifiedCOMPLETEDInfluence of Selenium on Prostate Cancer Related Biomarkers

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.