Bexicaserin

SKU:BHB21902208
Overview
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Bexicaserin (CAS 2035818-24-5) is an agonist supplied as a solid. Reported to act on 5-HT 2C Receptor. Relevant to GPCR/G Protein and Neuronal Signaling research. Molecular formula C15H19F2N3O, molecular weight 295.33 g/mol.
CAS Number 2035818-24-5
Molecular Weight 295.33 g/mol
Form Solid
Target 5-HT 2C Receptor
Storage 4°C as supplied; in solvent -80°C
Options selector
Catalog no. Size
HY-156601-5MG 5 mg
HY-156601-10MG 10 mg
HY-156601-25MG 25 mg
HY-156601-50MG 50 mg
HY-156601-100MG 100 mg
HY-156601-1MLX10MM 1 mL x 10 mM (in DMSO)
Available Options

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

  • Options: Size: 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 1 mL x 10 mM (in DMSO)
  • Lead time: shown per option in the variant selector.
  • Storage: 4°C, sealed storage, away from moisture and light. In solvent: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light).
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: refrigerate at 4°C as soon as possible.
Field Specification
Target 5-HT 2C Receptor
Alternative names LP352
CAS no. 2035818-24-5
Applications
  • Functional Assay (In Vitro)
Molecular weight 295.33
Molecular formula C15H19F2N3O
SMILES FC(F)CNC(C1=C2C3=C(C=C1)CNCCN3C[C@@H]2C)=O
Form Solid
Storage 4°C, sealed storage, away from moisture and light. In solvent: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light).
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-156601
Main SKU BHB21902208
Agonists

Compound Overview

Bexicaserin (LP352) is a 5-HT2C receptor agonist with potential for studying obesity and psychiatric-related disorders such as epilepsy[1][2]. It is supplied as a white to off-white solid (C15H19F2N3O, MW 295.33).

Physical & Chemical Properties

CAS Number 2035818-24-5
Molecular Formula C15H19F2N3O
Molecular Weight 295.33 g/mol
Appearance Solid
Color White to off-white
SMILES FC(F)CNC(C1=C2C3=C(C=C1)CNCCN3C[C@@H]2C)=O
Target 5-HT 2C Receptor
Signaling Pathway GPCR/G Protein; Neuronal Signaling
Solubility In Vitro: DMSO: 50 mg/mL (169.30 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Storage 4°C, sealed storage, away from moisture and light. In solvent: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light).
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Pędzich BD, et al. Effects of a psychedelic 5-HT2A receptor agonist on anxiety-related behavior and fear processing in mice. Neuropsychopharmacology. 2022 Jun;47(7):1304-1314.

[2]. Kaye R, et al. Searching for safer and more effective medications in the management of seizure disorders: a 5-HT2C superagonist[C]//EPILEPSIA. 111 RIVER ST, HOBOKEN 07030-5774, NJ USA: WILEY, 2023, 64: 315-315.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

SolventSolubilityNotes
DMSO50 mg/mL (169.30 mM)requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility)

Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); sealed storage, away from moisture and light; avoid repeated freeze-thaw cycles.

In Vivo

Choose the formulation that suits the animal model and route of administration; percentages are volume ratios of the final working solution. Start from a clear DMSO stock (see In Vitro above), add the co-solvents one at a time in the order listed, mixing after each addition, and prepare the working solution fresh on the day of dosing. If precipitation or phase separation occurs, gentle warming or sonication can help.

Protocol 1

Composition10% DMSO + 40% PEG300 + 5% Tween-80 + 45% saline
Result≥ 2.5 mg/mL (8.47 mM); clear solution
How to prepareGives a clear solution at ≥ 2.5 mg/mL (saturation not determined). For 1 mL of working solution: add 100 μL DMSO stock (25.0 mg/mL) to 400 μL PEG300; then 50 μL Tween-80; then 450 μL saline to bring the volume to 1 mL. Saline: dissolve 0.9 g sodium chloride in ddH2O and make up to 100 mL.

Protocol 2

Composition10% DMSO + 90% (20% SBE-β-CD in saline)
Result≥ 2.5 mg/mL (8.47 mM); clear solution
How to prepareGives a clear solution at ≥ 2.5 mg/mL (saturation not determined). For 1 mL of working solution: add 100 μL DMSO stock (25.0 mg/mL) to 900 μL 20% SBE-β-CD in saline. 20% SBE-β-CD in saline: dissolve 2 g SBE-β-CD powder in 10 mL saline until clear (4°C, store up to one week).

Protocol 3

Composition10% DMSO + 90% Corn Oil
Result≥ 2.5 mg/mL (8.47 mM); clear solution
How to prepareGives a clear solution at ≥ 2.5 mg/mL (saturation not determined). Use with caution if continuous dosing will exceed two weeks. For 1 mL of working solution: add 100 μL DMSO stock (25.0 mg/mL) to 900 μL corn oil.

Data provided by the manufacturer.

In Vitro

At 10 μM for 24 or 48 hours, Bexicaserin acts as a superagonist of the 5-HT2C receptor (a ligand eliciting a larger response than the endogenous agonist) and its Ki is 44 nM. In dynamic mass redistribution (DMR) assays, Bexicaserin elicited a maximal cellular response in HEK293 cells expressing the human 5-HT2C receptor, higher than the response elicited by the endogenous agonist 5-HT[2].

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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