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565771 InSolution™ γ-Secretase Inhibitor X - Calbiochem

InSolution™ γ-Secretase Inhibitor X is a 1 mM solution in DMSO. A highly potent inhibitor of g-secretase (IC₅₀ = 17, 48, 67 nM for Aβtotal, Aβ40 & Aβ42 in SHSY5Y cells overexpressing spβA4CTF).

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

Sinónimos: L-685,458, {1S-Benzyl-4R-[1-(1S-carbamoyl-2-phenethylcarbamoyl)-1S-3-methylbutylcarbamoyl]-2R-hydroxy-5-phenylpentyl}carbamic Acid tert-butyl Ester

Primary Target: Aβtotal
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565771
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Descripción

Replacement Information

Tabla espec. clave

Empirical Formula
C₃₉H₅₂N₄O₆

Precios y disponibilidad

Número de referencia DisponiblidadEmbalaje Cant./Env. Precio Cantidad
565771-250UG
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      565771-500UG
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          Contact Customer Service

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          Description
          OverviewA cell-permeable hydroxyethylene dipeptide isostere that acts as a highly specific and a potent inhibitor of γ-secretase (Aβtotal IC50 = 17 nM, Aβ40 IC50 = 48 nM, and Aβ42 IC50 = 67 nM in SHSY5Y cells overexpressing spβA4CTF). Binds to presenilin and blocks Notch intracellular domain production. Functions as a transition state analog mimic at the catalytic site of an aspartyl protease, however, it exhibits over 100-fold greater selectivity for γ-secretase than for cathepsin D.
          Catalogue Number565771
          Brand Family Calbiochem®
          SynonymsL-685,458, {1S-Benzyl-4R-[1-(1S-carbamoyl-2-phenethylcarbamoyl)-1S-3-methylbutylcarbamoyl]-2R-hydroxy-5-phenylpentyl}carbamic Acid tert-butyl Ester
          References
          ReferencesWeidemann, A., et al. 2002. Biochemistry 41, 2825.
          Doerfler, P., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 9312.
          Li, Y.M., et al. 2000. Proc. Natl. Acad. Sci. USA 97, 6138.
          Shearman, M.S., et al. 2000. Biochemistry 39, 8698.
          Product Information
          ATP CompetitiveN
          FormLiquid
          FormulationA 1 mM (250 µg in 372 µl or 500 µg in 744 µl) solution in DMSO.
          Hill FormulaC₃₉H₅₂N₄O₆
          Chemical formulaC₃₉H₅₂N₄O₆
          ReversibleN
          Structure formula ImageStructure formula Image
          Quality LevelMQ100
          Applications
          Biological Information
          Primary TargetAβtotal
          Primary Target IC<sub>50</sub>Aβtotal 17 nM, Aβ40 48 nM, and Aβ42 67 nM in SHSY5Y cells overexpressing spβA4CTF
          Purity≥90% 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 -20°C
          Protect from Light Protect from light
          Protect from Moisture Protect from moisture
          Do not freeze Ok to freeze
          Special InstructionsFollowing initial thaw, aliquot and freeze (-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
          565771-250UG 04055977267839
          565771-500UG 04055977267846

          Documentation

          Licencias necesarias

          Título
          CARTA DE USO GENERAL 2016
          PRODUCTO REGULADO POR LA SAGARPA
          PRODUCTO REGULADO POR LA SECRETARÍA DE SALUD

          InSolution™ γ-Secretase Inhibitor X - Calbiochem Ficha datos de seguridad (MSDS)

          Título

          Ficha técnica de seguridad del material (MSDS) 

          InSolution™ γ-Secretase Inhibitor X - Calbiochem Certificados de análisis

          CargoNúmero de lote
          565771

          Referencias bibliográficas

          Visión general referencias
          Weidemann, A., et al. 2002. Biochemistry 41, 2825.
          Doerfler, P., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 9312.
          Li, Y.M., et al. 2000. Proc. Natl. Acad. Sci. USA 97, 6138.
          Shearman, M.S., et al. 2000. Biochemistry 39, 8698.
          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-September-2008 RFH
          SynonymsL-685,458, {1S-Benzyl-4R-[1-(1S-carbamoyl-2-phenethylcarbamoyl)-1S-3-methylbutylcarbamoyl]-2R-hydroxy-5-phenylpentyl}carbamic Acid tert-butyl Ester
          DescriptionA cell-permeable hydroxyethylene dipeptide isostere that acts as a potent and highly specific inhibitor of γ-secretase (Aβ total IC50 = 17 nM; Aβ40 IC50 = 48 nM; and Aβ42 IC50 = 67 nM in SH-SY5Y cells overexpressing spβA4CTF). Binds to presenilin and blocks Notch intracellular domain production. Also reported to block the formation of εCTF, resulting in the accumulation of α- and βCTF. Functions as a transition state analog mimic at the catalytic site of an aspartyl protease, however, it exhibits over 100-fold greater selectivity for γ-secretase than for cathepsin D.
          FormLiquid
          FormulationA 1 mM (250 µg in 372 µl or 500 µg in 744 µl) solution in DMSO.
          Intert gas (Yes/No) Packaged under inert gas
          Chemical formulaC₃₉H₅₂N₄O₆
          Structure formulaStructure formula
          Purity≥90% by HPLC
          Storage Protect from moisture
          Protect from light
          -20°C
          Do Not Freeze Ok to freeze
          Special InstructionsFollowing initial thaw, aliquot and freeze (-20°C).
          Toxicity Standard Handling
          ReferencesWeidemann, A., et al. 2002. Biochemistry 41, 2825.
          Doerfler, P., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 9312.
          Li, Y.M., et al. 2000. Proc. Natl. Acad. Sci. USA 97, 6138.
          Shearman, M.S., et al. 2000. Biochemistry 39, 8698.