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516481 Pepstatin A, Synthetic - CAS 26305-03-3 - Calbiochem

Pepstatin A, Synthetic, CAS 26305-03-3, is a reversible inhibitor of aspartic proteases. Inhibits cathepsin D, pepsin, and renin.

Pepstatin A, Synthetic - CAS 26305-03-3 - Calbiochem: Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles.

Sinónimos: Iva-Val-Val-Sta-Ala-Sta, Isovaleryl-Val-Val-4-amino-3-hydroxy-6-methylheptanoyl-Ala-4-amino-3-hydroxy-6-methylheptanoic Acid

Primary Target: cathepsin D
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516481
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Descripción

Replacement Information

Tabla espec. clave

CAS #Empirical Formula
26305-03-3C₃₄H₆₃N₅O₉

Precios y disponibilidad

Número de referencia DisponiblidadEmbalaje Cant./Env. Precio Cantidad
516481-100MG
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      516481-25MG
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          516481-5MG
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          Debe confirmarse disponibilidad
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              Description
              OverviewA reversible inhibitor of aspartic proteases. Inhibits cathepsin D, pepsin, and renin. Reported to block apoptosis induced by CA-074 (Cat. No. 205530) in PC12 cell lines. Also available as a 25 mM solution in DMSO (Cat. No. 508437).
              Effective concentration: 1.0 µM.
              Catalogue Number516481
              Brand Family Calbiochem®
              SynonymsIva-Val-Val-Sta-Ala-Sta, Isovaleryl-Val-Val-4-amino-3-hydroxy-6-methylheptanoyl-Ala-4-amino-3-hydroxy-6-methylheptanoic Acid
              References
              ReferencesIsahara, K., et al. 1999. Neuroscience 91, 233.
              Kanamori, S., et al. 1998. Biochem. Biophys. Res. Commun. 251, 204.
              Szewczuk, Z., et al. 1992. Int. J. Pept. Prot. Res. 40, 233.
              Carraway, R.E., et al. 1991. Peptides 12, 107.
              Eid, M., et al. 1981. Biochem. J. 197, 465.
              Umezawa, H., et al. 1970. J. Antibiot. 23, 259.
              Product Information
              CAS number26305-03-3
              ATP CompetitiveN
              FormWhite solid
              Hill FormulaC₃₄H₆₃N₅O₉
              Chemical formulaC₃₄H₆₃N₅O₉
              HS Code2924 19 99
              Optical rotationOptical rotation: -90.0 ± 5° (c = 0.5, MeOH, 20°C).
              ReversibleY
              Quality SegmentMQ100
              Applications
              Biological Information
              Primary Targetcathepsin D
              Primary Target IC<sub>50</sub>EC50 = 1.0 µM in blocking apoptosis induced by CA-074 in PC12 cell lines
              Purity≥98% by HPLC
              Physicochemical Information
              Cell permeableN
              Dimensions
              Materials Information
              Toxicological Information
              Safety Information according to GHS
              RTECSSC6155000
              Safety Information
              Product Usage Statements
              Storage and Shipping Information
              Ship Code Ambient Temperature Only
              Toxicity Standard Handling
              Storage +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 4 months at -20°C.
              Packaging Information
              Transport Information
              Supplemental Information
              Specifications
              Global Trade ITEM Number
              Número de referencia GTIN
              516481-100MG 04055977198812
              516481-25MG 07790788055837
              516481-5MG 04055977198836

              Documentation

              Pepstatin A, Synthetic - CAS 26305-03-3 - Calbiochem Ficha datos de seguridad (MSDS)

              Título

              Ficha técnica de seguridad del material (MSDS) 

              Pepstatin A, Synthetic - CAS 26305-03-3 - Calbiochem Certificados de análisis

              CargoNúmero de lote
              516481

              Referencias bibliográficas

              Visión general referencias
              Isahara, K., et al. 1999. Neuroscience 91, 233.
              Kanamori, S., et al. 1998. Biochem. Biophys. Res. Commun. 251, 204.
              Szewczuk, Z., et al. 1992. Int. J. Pept. Prot. Res. 40, 233.
              Carraway, R.E., et al. 1991. Peptides 12, 107.
              Eid, M., et al. 1981. Biochem. J. 197, 465.
              Umezawa, H., et al. 1970. J. Antibiot. 23, 259.

              Folleto

              Cargo
              Western Blotting Tools

              Licencias necesarias e Información técnica

              Cargo
              Protein Blotting Handbook: 6th Edition
              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.

              Revision11-October-2013 JSW
              SynonymsIva-Val-Val-Sta-Ala-Sta, Isovaleryl-Val-Val-4-amino-3-hydroxy-6-methylheptanoyl-Ala-4-amino-3-hydroxy-6-methylheptanoic Acid
              DescriptionA reversible inhibitor of aspartic proteases. Inhibits cathepsin D, pepsin, and renin. Reported to block apoptosis induced by CA-074 (Cat. No. 205530) in PC12 cells. Effective concentration: 1 µM.
              FormWhite solid
              Recommended reaction conditions
              Activity:
              Activity is measured by inhibition of pepsin. 1 U corresponds to the amount of inhibitor that reduces the activity of pepsin by 1 U (1 U of enzyme corresponds to the amount of enzyme that results in the increases the absorbance at 280 nm by 0.001 per min at pH 2.0, 37°C.)
              CAS number26305-03-3
              RTECSSC6155000
              Chemical formulaC₃₄H₆₃N₅O₉
              Purity≥98% by HPLC
              SolubilityDMSO (1 mg/ml) or Methanol (1 mg/ml)
              Storage +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 4 months at -20°C.
              Toxicity Standard Handling
              Merck USA index14, 7147
              ReferencesIsahara, K., et al. 1999. Neuroscience 91, 233.
              Kanamori, S., et al. 1998. Biochem. Biophys. Res. Commun. 251, 204.
              Szewczuk, Z., et al. 1992. Int. J. Pept. Prot. Res. 40, 233.
              Carraway, R.E., et al. 1991. Peptides 12, 107.
              Eid, M., et al. 1981. Biochem. J. 197, 465.
              Umezawa, H., et al. 1970. J. Antibiot. 23, 259.