AZD-9056 hydrochloride

SKU:BHB21300038
Overview
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AZD-9056 hydrochloride (CAS 345303-91-5) is AZD-9056 is a potent and selective, orally bioavailable antagonist of the purinergic P2X7 receptor, shown to inhibit YoPro1 uptake in HEK-hP2X7 cells with IC50 of 11.2 nM1. Supplied as Lyophilized Powder (purity >97%, solubility Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min)). Commonly used in Neuroscience studies, including binding assays and second-messenger readouts.
Target P2X7 receptor
Cas No 345303-91-5
concentration 1-100 nM.
purity >97%
Molecular Formula C24H36Cl2N2O2 (C24H35ClN2O2 · HCl).
Form Lyophilized Powder
Available Options

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

  • Options: Size (4) - 1 mg, 10 mg, 25 mg, 5 mg; Quantity: 1
  • Lead time: typically ships in 1-2 business days; timing may vary by selected option.
  • Storage: After reconstitution: The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods (up to 6 months), small aliquots should be stored at -20°C. We do not recommend storing the product in working solutions for longer than a few days. Avoid multiple freeze-thaw cycles. Storage of solutions: -20°C. It is recommended to aliquot stock solutions to prevent repeated thawing and freezing.
  • Shipping: Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Options selector
Catalog no. Size Quantity
A-425-1MG-1 1 mg
A-425-10MG-1 10 mg
A-425-25MG-1 25 mg
A-425-5MG-1 5 mg
Field Specification
Activity
  • Antagonist
Cas No. 345303-91-5
Concentration 1-100 nM.
Form Lyophilized Powder
Product Type
  • Biochemicals
  • Small Molecules
Purity >97%
Reconstitution Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
Shipping Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
Solubility Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
Source Synthetic
Storage After reconstitution: The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods (up to 6 months), small aliquots should be stored at -20°C. We do not recommend storing the product in working solutions for longer than a few days. Avoid multiple freeze-thaw cycles. Storage of solutions: -20°C. It is recommended to aliquot stock solutions to prevent repeated thawing and freezing.
Target P2X7 receptor

Product details

  • Chemical name: N-(1-adamantylmethyl)-2-chloro-5-[3-(3-hydroxypropylamino)propyl]benzamide hydrochloride.
  • Also known as: N-(1-Adamantylmethyl)-2-chloro-5-[3-(3-hydroxypropylamino)propyl]benzamide hydrochloride
  • CAS number: 345303-91-5
  • Molecular formula: C24H36Cl2N2O2 (C24H35ClN2O2 · HCl).
  • Purity: >97%
  • Concentration: 1-100 nM.
  • Form: Lyophilized Powder
  • Solubility: Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
  • Reconstitution: Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
  • Shipping: Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
  • Target: P2X7 receptors
  • Source: Synthetic
  • Activity: AZD-9056 is a potent and selective, orally bioavailable antagonist of the purinergic P2X7 receptor, shown to inhibit YoPro1 uptake in HEK-hP2X7 cells with IC50 of 11.2 nM1. AZD-9056 shows pain-relieving and anti-inflammatory effects in vivo2.
  • Alternative names: N-(1-Adamantylmethyl)-2-chloro-5-[3-(3-hydroxypropylamino)propyl]benzamide hydrochloride

Scientific background

AZD-9056 hydrochloride is an adamantane amide that acts as a potent and selective antagonist of P2X7 receptors. It inhibits YoPro1 (membrane-impermeable fluorescent dye) uptake in HEK-hP2X7 cells with IC50 value of 11.2 nM1. Studies show that treatment with AZD-9056 exerts pain-relieving and anti-inflammatory effects1,2.The P2X7 receptor is a member of the ligand-gated ion channels activated by extracellular ATP. There are seven receptor subtypes: P2X1-P2X7. P2X7 receptors participate in a variety of cellular responses such as membrane permeabilization, activation of caspases, cytokine release, cell proliferation, and apoptosis. P2X7 receptors are highly expressed throughout autonomic, sensory and central neurons and in visceral smooth muscle, immune cells and epithelia3,4.

Lead time: 1-2 Business Days

Country of origin: Israel/IL

Applications key

Application key: FC- Flow cytometry, IFC- Indirect flow cytometry, IHC- Immunohistochemistry,LCI- Live cell imaging, Calcium imaging assay,Cell survival assay, Electrophysiology, Neurite outgrowth assay.

Bioassay tested: Yes

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  • 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

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