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401481 IKK-2 Inhibitor IV - CAS 507475-17-4 - Calbiochem

The IKK-2 Inhibitor IV, also referenced under CAS 507475-17-4, controls the biological activity of IKK-2. This small molecule/inhibitor is primarily used for Inflammation/Immunology applications.

Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles.

Sinónimos: [5-(p-Fluorophenyl)-2-ureido]thiophene-3-carboxamide, TPCA-1

Primary Target: IKK-2
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401481
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Descripción

Replacement Information

Tabla espec. clave

CAS #Empirical Formula
507475-17-4C₁₂H₁₀FN₃O₂S

Precios y disponibilidad

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401481-500UG
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      Description
      OverviewA cell-permeable ureidocarboxamido thiophene compound that acts as a potent, reversible, and ATP-competitive inhibitor of IKK-2 (IC50 = 18 nM) with selectivity over IKK-1, JNK and p38 MAPK. Inhibits TNF-α production in human monocytes (IC50 in the range of 0.15-2.5 µM) and blocks IL-8 and IL-6 production by synovial fibroblasts (IC50 = 100 nM). Further reduces paw oedema in rat arthritis model (~100% inhibition at a dose of 30 mg per kg). A 10 mM (500 µg/179 µl) solution of IKK-2 Inhibitor IV (Cat. No. 401484) in DMSO is available.
      Catalogue Number401481
      Brand Family Calbiochem®
      Synonyms[5-(p-Fluorophenyl)-2-ureido]thiophene-3-carboxamide, TPCA-1
      References
      ReferencesPodolin, P.L., et al. 2005. J. Pharmacol. Exp. Ther. 312, 373.
      Karin, M., et al. 2004. Nat. Rev. Drug Discov. 3, 17.
      Roshak, A.K., et al. 2002. Inflamm. Res. 51, S4.
      Product Information
      CAS number507475-17-4
      ATP CompetitiveY
      FormWhite to pale yellow solid
      Hill FormulaC₁₂H₁₀FN₃O₂S
      Chemical formulaC₁₂H₁₀FN₃O₂S
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetIKK-2
      Primary Target IC<sub>50</sub>18 nM against IKK-2
      Purity≥95% by HPLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Standard Handling
      Storage +2°C to +8°C
      Protect from Light Protect from light
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Número de referencia GTIN
      401481-500UG 04055977211962

      Documentation

      Licencias necesarias

      Título
      PRODUCTO REGULADO POR LA SECRETARÍA DE SALUD

      IKK-2 Inhibitor IV - CAS 507475-17-4 - Calbiochem Ficha datos de seguridad (MSDS)

      Título

      Ficha técnica de seguridad del material (MSDS) 

      IKK-2 Inhibitor IV - CAS 507475-17-4 - Calbiochem Certificados de análisis

      CargoNúmero de lote
      401481

      Referencias bibliográficas

      Visión general referencias
      Podolin, P.L., et al. 2005. J. Pharmacol. Exp. Ther. 312, 373.
      Karin, M., et al. 2004. Nat. Rev. Drug Discov. 3, 17.
      Roshak, A.K., et al. 2002. Inflamm. Res. 51, S4.
      Ficha técnica

      Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

      Revision10-July-2023 JSW
      Synonyms[5-(p-Fluorophenyl)-2-ureido]thiophene-3-carboxamide, TPCA-1
      DescriptionA cell-permeable, reversible, ATP-competitive, and potent inhibitor of IKK-2 (IC50 = 18 nM) that exhibits selectivity over IKK-1, JNK, and p38 MAPK. Inhibits TNF-α production in human monocytes (IC50 in the range of 0.15-2.5 µM) and blocks IL-8 and IL-6 production by synovial fibroblasts (IC50 = 100 nM). Shown to reduce paw oedema in rat arthritis model (~100% inhibition at a dose of 30 mg per kg).
      FormWhite to pale yellow solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number507475-17-4
      Chemical formulaC₁₂H₁₀FN₃O₂S
      Structure formulaStructure formula
      Purity≥95% by HPLC
      SolubilityDMSO (10 mg/ml)
      Storage Protect from light
      +2°C to +8°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
      Toxicity Standard Handling
      ReferencesPodolin, P.L., et al. 2005. J. Pharmacol. Exp. Ther. 312, 373.
      Karin, M., et al. 2004. Nat. Rev. Drug Discov. 3, 17.
      Roshak, A.K., et al. 2002. Inflamm. Res. 51, S4.