Vildagliptin

SKU:BHB11900345
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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Vildagliptin is a research-grade small-molecule inhibitor of Anti-diabetic supporting Neuroscience and Neurodegeneration research. Supplied as a white powder with >98% purity (CAS 274901-16-5, MW 303.4) dissolvable in DMSO; store at -20°C. For research use only.
Cas No. 274901-16-5
Molecular Formula C17H25N3O2
Purity >98% (HPLC); NMR (Conforms)
Application Notes Anti-diabetic agent
Options selector
Catalog no. Size
SIH-567-20MG 20 mg
SIH-567-100MG 100 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size (2) — 100 mg, 20 mg.
  • Lead time: options listed as “in stock at manufacturer” typically ship in 2-3 business days; other statuses may take longer.
  • Storage: -20ºC
  • Shipping: ships at ambient temperature.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Alternative names (S)-1-[N-(3-hydroxy-1-adamantyl)glycyl]pyrrolidine-2-carbonitrile; LAF237
CAS no. 274901-16-5
Applications
  • Functional Assay (In Vitro)
Source Synthetic
Molecular weight 303.4
Molecular formula C17H25N3O2
Purity >98% (HPLC); NMR (Conforms)
Bioactivity Inhibitor
Activity
  • Inhibitor
Solubility May be dissolved in DMSO (45 mg/ml); or DMF (20 mg/ml); or ethanol (20 mg/ml)
SMILES C1C[C@@H](C#N)N(C1)C(=O)CN[C@]12C[C@@H]3C[C@H](C1)C[C@@](C3)(C2)O
InChIKey SYOKIDBDQMKNDQ-NHMCJKAESA-N
Form White powder
Storage -20ºC
Shipping Shipped Ambient
Catalog no. (Mfr.) SIH-567
Main SKU BHB11900345

Vildagliptin is a potent inhibitor of dipeptidyl peptidase IV (DPP-IV), an enzyme responsible for degrading glucagon-like peptide-1 (GLP-1). By delaying GLP-1 degradation, Vildagliptin enhances insulin secretion and suppresses glucagon release, thereby improving glycemic control. In neurodegenerative disease research, Vildagliptin has shown promise in ameliorating cognitive deficits in models of Alzheimer’s disease. It also exhibits protective effects on pancreatic β-cells by reducing endoplasmic reticulum stress. These neuroprotective and anti-inflammatory properties make Vildagliptin a candidate for exploring the metabolic-neurodegenerative interface, particularly in diabetes-associated cognitive decline.

Signal Word:

  • Warning GHS Classifcation: GHS07 Acute toxicity (oral, dermal, inhalation), category 4
  • Skin irritation, category 2
  • Eye irritation, category 2
  • Skin sensitisation, category 1
  • Specific Target Organ Toxicity – Single exposure, category 3 Hazard statement(s):
  • H302 H315 Causes skin irritation.
  • H319 Causes serious eye irritation.
  • H335 May cause respiratory irritation.

Precautionary statement(s):

P301 + P312 + P330-P305 + P351 + P338

Vildagliptin (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-567)

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

1. B Balas et al. J. Clin. Endocrinol. Metab. 2007 92:1249
2. B Ahren et al. J. Clin. Endocrinol. Metab. 2004 89:2078
3. J Kosaraju et al. J. Pharm. Pharmacol. 2013 65:1773
4. S Shimizu et al. J. Mol. Endocrinol. 2012 49:125

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