Millipore Sigma Vibrant Logo

110145 D-erythro-Sphingosine, N-Acetyl- - CAS 3102-57-6 - Calbiochem

Biologically active, cell-permeable, non-physiological ceramide analog.

FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.

Synonymes: C₂ Ceramide

View Products on Sigmaaldrich.com
110145
Voir les Prix & la Disponibilité

Aperçu

Replacement Information

Tableau de caractéristiques principal

CAS #Empirical Formula
3102-57-6C₂₀H₃₉NO₃

Prix & Disponibilité

Référence DisponibilitéConditionnement Qté Prix Quantité
110145-5MG
Récupération des données relatives à la disponibilité...
—
Disponibilité limitée Disponibilité limitée
En stock 
Interrompu(e)
Disponible en quantités limitées
Disponibilité à confirmer
    Pour le restant : Nous vous tiendrons informé
      Pour le restant : Nous vous tiendrons informé
      Nous vous tiendrons informé
      Contacter le Service Clients
      Contact Customer Service

      		 Ampoule plast. 5 mg
      Prix en cours de récupération
      Le prix n'a pas pu être récupéré
      La quantité minimale doit être un multiple de
      Maximum Quantity is
      À la validation de la commande Plus d'informations
      Vous avez sauvegardé ()
       
      —
      Demander le prix
      		 —
      Description
      OverviewBiologically active, cell-permeable, non-physiological ceramide analog. Inhibits cell growth and induces apoptosis in HL-60 cells. Induces intranucleosomal DNA fragmentation. An activator of heterotrimeric protein phosphatase 2A (PP2A). Stimulates a cytosolic serine/threonine protein phosphatase in T9 cells at concentrations as low as 100 nM. Activates stress activated protein kinase (SAPK) in HL-60 human promyelocytic cells.
      Catalogue Number110145
      Brand Family Calbiochem®
      SynonymsC₂ Ceramide
      References
      ReferencesWestwick, J.K., et al. 1995. J. Biol. Chem. 270, 22689.
      Cifone, M.G., et al. 1994. J. Exp. Med. 180, 1547.
      Hannun, Y.A. 1994. J. Biol. Chem. 269, 3125.
      Bielawska, A., et al. 1993. J. Biol. Chem. 268, 26226.
      Obeid, L.M., et al. 1993. Science 259, 1769.
      Ballou, L.R., et al. 1992. J. Biol. Chem. 267, 20044.
      Dobrowsky, R.T., and Hannun, Y.A. 1992. J. Biol. Chem. 267, 5048.
      Product Information
      CAS number3102-57-6
      ATP CompetitiveN
      FormWhite to off-white solid
      Hill FormulaC₂₀H₃₉NO₃
      Chemical formulaC₂₀H₃₉NO₃
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetInhibits cell growth and induces apoptosis in HL-60 cells
      Purity≥98% by TLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      R PhraseR: 36/37/38

      Irritating to eyes, respiratory system and skin.
      S PhraseS: 26-36

      In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
      Wear suitable protective clothing.
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Irritant
      Storage -20°C
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). DMSO stock solutions are stable for up to 1 month at -20°C. Alcohol stock solutions are stable for <1 week at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Référence GTIN
      110145-5MG 07790788055585

      Documentation

      D-erythro-Sphingosine, N-Acetyl- - CAS 3102-57-6 - Calbiochem Certificats d'analyse

      TitreNuméro de lot
      110145

      Références bibliographiques

      Aperçu de la référence bibliographique
      Westwick, J.K., et al. 1995. J. Biol. Chem. 270, 22689.
      Cifone, M.G., et al. 1994. J. Exp. Med. 180, 1547.
      Hannun, Y.A. 1994. J. Biol. Chem. 269, 3125.
      Bielawska, A., et al. 1993. J. Biol. Chem. 268, 26226.
      Obeid, L.M., et al. 1993. Science 259, 1769.
      Ballou, L.R., et al. 1992. J. Biol. Chem. 267, 20044.
      Dobrowsky, R.T., and Hannun, Y.A. 1992. J. Biol. Chem. 267, 5048.

      Brochure

      Titre
      Bioactive Lipids Technical Bulletin
      Caspases and other Apoptosis Related Tools Brochure
      Fiche technique

      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.

      Revision07-April-2008 RFH
      SynonymsC₂ Ceramide
      DescriptionBiologically active, cell-permeable, non-physiological ceramide analog. Inhibits cell growth and induces apoptosis of HL-60 cells. Induces intranucleosomal DNA fragmentation. An activator of heterotrimeric protein phosphatase 2A. Stimulates a cytosolic serine/threonine protein phosphatase in T9 cells at concentrations as low as 100 nM. Activates stress-activated protein (SAP) kinase in HL-60 human promyelocytic cells.
      FormWhite to off-white solid
      CAS number3102-57-6
      Chemical formulaC₂₀H₃₉NO₃
      Structure formulaStructure formula
      Purity≥98% by TLC
      SolubilityDMSO (25 mg/ml), Ethanol (5 mg/ml) or Methanol (5 mg/ml). When diluting into aqueous solution, sonication may be necessary to achieve a uniform suspension.
      Storage -20°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). DMSO stock solutions are stable for up to 1 month at -20°C. Alcohol stock solutions are stable for <1 week at -20°C.
      Toxicity Irritant
      ReferencesWestwick, J.K., et al. 1995. J. Biol. Chem. 270, 22689.
      Cifone, M.G., et al. 1994. J. Exp. Med. 180, 1547.
      Hannun, Y.A. 1994. J. Biol. Chem. 269, 3125.
      Bielawska, A., et al. 1993. J. Biol. Chem. 268, 26226.
      Obeid, L.M., et al. 1993. Science 259, 1769.
      Ballou, L.R., et al. 1992. J. Biol. Chem. 267, 20044.
      Dobrowsky, R.T., and Hannun, Y.A. 1992. J. Biol. Chem. 267, 5048.