Safiglipron Research Reference

Catalog classification, reference sizes, lab math links, and source-backed data. Educational use only — not medical advice.

Researched for: PepTools vendor-neutral scientific reference catalog

Glucagon-like peptide-1 receptor agonist; antidiabetic compound Reference needs_revision Best effort · source review pending

Also known as: HRS-7535, HRS7535, GLP-1 receptor agonist 15, EX-A16881, CHEMBL6160879

Best-effort research profile: this record has not passed full two-source scientific verification. Descriptive fields, research protocols, storage/handling notes, and interaction guidance below are shown with their evidence labels, but calculator presets and exact dosing math remain hidden until the record is verified or reaches Community-Supported status.

Quick Facts

Reference Sizes
Not standardized / source review pending

Best-Effort Research Profile

Safiglipron is a structurally distinct, once-daily oral small-molecule GLP-1 receptor agonist. It has been evaluated in randomized clinical studies in adults with type 2 diabetes and obesity, including phase 2 and phase 3 studies. The compound is identified by the molecular formula C32H31ClFN3O5 and CAS Registry Number 2757506-39-9.

Source review pending. This descriptive profile is shown from the available source material as a best-effort educational reference. It has not passed the full verification bar and is not a dosing instruction, medical claim, or treatment recommendation.

Research Profile

Administration Routes (Research)
oral

Reported Research Effects

Reflects preclinical/research literature context only. Not a medical claim, dosing instruction, or treatment recommendation.

Research Notes

Evidence reviewed supports research use as a reference compound. Published studies report once-daily oral clinical regimens including 15–90 mg in a phase 2 type 2 diabetes study, 30–180 mg in a phase 2 obesity study, and 30, 60, or 90 mg in the OUTSTAND-1 phase 3 study; these are study regimens and not prescribing recommendations. Reliable authoritative sources reviewed did not provide a validated catalog storage condition, aqueous solubility value, or consistently reported terminal half-life for the compound.

Supplementary research context only. Not medical advice or a treatment recommendation.

Registry Identifiers

CAS RN 2757506-39-9; PubChem CID 166094939; molecular formula C32H31ClFN3O5; molecular weight 592.1 g/mol; InChIKey YPJSZRLSBAIGIE-PZGXJGMVSA-N; ChEMBL CHEMBL6160879; IUPAC name 2-[[4-[(3S)-3-(4-chloro-2-fluorophenyl)-2,3-dihydro-1,4-benzodioxin-5-yl]piperidin-1-yl]methyl]-3-[[(2S)-oxetan-2-yl]methyl]benzimidazole-5-carboxylic acid

Source-Backed Observations

Safiglipron is listed as a proposed INN in WHO Proposed INN List 134. Published clinical literature identifies safiglipron as HRS-7535. Human studies have used once-daily oral administration, with dose-escalation or titration regimens in some protocols.

Reflects published research. Educational reference — not a recommendation for use.

Sources Under Review

Safiglipron: PubChem Compound Summary
https://pubchem.ncbi.nlm.nih.gov/compound/166094939 (accessed 2026-09-30)
Oral small-molecule GLP-1 receptor agonist safiglipron in early type 2 diabetes: a randomized, double-blind, placebo-controlled trial
https://www.nature.com/articles/s41591-026-04651-9 (accessed 2026-09-30)
HRS-7535 for Type 2 Diabetes Inadequately Controlled With Metformin: A Randomized Clinical Trial
https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2849835 (accessed 2026-09-30)
HRS-7535, an oral small-molecule GLP-1 receptor agonist, in Chinese adults with obesity without diabetes: a randomized, double-blind, placebo-controlled phase 2 trial
https://www.nature.com/articles/s41467-026-73018-y (accessed 2026-09-30)

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Related Research Articles

Published articles on this site that mention Safiglipron or one of its catalog aliases.

Related Research Tools

Research Use Only. All content is for educational and research reference only. Not medical advice, a treatment recommendation, or guidance on human use. Compounds are not FDA-approved drugs unless specifically noted.

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