Co 102862

SKU:BHB21300078
Overview
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Co 102862 (CAS 181144-66-1) is a potent, broad spectrum and state-dependent blocker of neuronal voltage-gated Na+ channels that interacts selectively with inactivated states as opposed to resting states of the channel1. Supplied as Lyophilized powder (purity >96% (HPLC), solubility DMSO. Centrifuge all product preparations before use (10000 x g 5 min)). Commonly used in Neuroscience studies, including patch-clamp electrophysiology and ion channel screening.
Target NaV channel
Cas No 181144-66-1
concentration 0.1-200 μM
purity >96% (HPLC)
Molecular Formula C14H12FN3O2.
Form Lyophilized powder.
Options selector
Catalog no. Size Quantity
C-160-10MG-1 10 mg
C-160-25MG-1 25 mg
C-160-5MG-1 5 mg
C-160-50MG-1 50 mg
Available Options

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

  • Options: Size (4) - 10 mg, 25 mg, 5 mg, 50 mg; Quantity: 1
  • Lead time: typically ships in 1-2 business days; timing may vary by selected option.
  • Storage: Before reconstitution: The product is shipped as a lyophilized powder at room temperature. Upon receipt, store the product at -20°C. Protect from moisture. 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: Up to four weeks at 4°C or three months at -20°C.
  • 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.
Field Specification
Mfr No C-160
Accession Number P26441
Activity
  • Blocker
Cas No. 181144-66-1
Concentration 0.1-200 μM
Form Lyophilized powder.
Product Type
  • Biochemicals
  • Small Molecules
Purity >96% (HPLC)
Reconstitution DMSO. Centrifuge all product preparations before use (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 DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
Source Synthetic
Storage Before reconstitution: The product is shipped as a lyophilized powder at room temperature. Upon receipt, store the product at -20°C. Protect from moisture. 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: Up to four weeks at 4°C or three months at -20°C.
Target NaV channel

Product details

  • Chemical name: 2-[[4-(4-Fluorophenoxy)phenyl]methylene]hydrazinecarboxamide.
  • Also known as: V102862
  • CAS number: 181144-66-1
  • Molecular formula: C14H12FN3O2.
  • Purity: >96% (HPLC)
  • Concentration: 0.1-200 μM
  • Form: Lyophilized powder.
  • Solubility: DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
  • Reconstitution: DMSO. Centrifuge all product preparations before use (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: NaV Na+ channels
  • Source: Synthetic
  • Activity: Co 102862 is a potent, broad spectrum and state-dependent blocker of neuronal voltage-gated Na+ channels that interacts selectively with inactivated states as opposed to resting states of the channel1. IC50 values are 0.28-15.9 µM in rat hippocampal neurons2. It is an anticonvulsant, demonstrating potent activity in rodent models of tonic/clonic and partial-complex seizures3.
  • Alternative names: V102862

Peptide confirmation

Confirmed by amino acid analysis and mass spectrometry

Scientific background

Voltage-gated Na+ channels play key roles in determining neuronal excitability1,2. Voltage- and use-dependent blockage of voltage-gated Na+ channels appear to be important in the mechanism of action of many anticonvulsants (e.g. phenytoin (PHT), carbamazepine (CBZ) and lamotrigine (LTG)), local anesthetics (e.g. lidocaine and bupivacaine) and Class I antiarrhythmics3-10.Co 102862 is a potent, broad spectrum and state-dependent blocker of neuronal voltage-gated Na+ channels that interacts selectively with inactivated states as opposed to resting states of the channel11. IC50 values are 0.28-15.9 μM in rat hippocampal neurons11.Co 102862 is an anticonvulsant, demonstrating potent activity in rodent models of tonic/clonic and partial-complex seizures12.

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

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

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