Millipore Sigma Vibrant Logo

239802 Curcumin, Curcuma longa L. - CAS 458-37-7 - Calbiochem

A cell-permeable and irreversible antitumor and anti-inflammatory agent that acts as an inhibitor of 5-lipoxygenase (IC₅₀ = 8 µM) and cyclooxygenase (IC₅₀ = 52 µM).

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

Sinónimos: 1,7-Bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione, NOD2 Signaling Inhibitor I, Nucleotide-binding Oligomerization Domain 2 Signaling Inhibitor I, Histone Acetyltransferase Inhibitor I, HAT Inhibitor I, p300/CBP Inhibitor I

Primary Target: 5-lipoxygenase
View Products on Sigmaaldrich.com
239802
Ver precios y disponibilidad

Descripción

Replacement Information

Tabla espec. clave

CAS #Empirical Formula
458-37-7C₂₁H₂₀O₆

Precios y disponibilidad

Número de referencia DisponiblidadEmbalaje Cant./Env. Precio Cantidad
239802-100MG
Comprobando disponibilidad...
—
Disponibilidad a confirmar Disponibilidad a confirmar
Ingrese cantidad 
Suspendido
Cantidades limitadas disponibles
Debe confirmarse disponibilidad
    El resto: se avisará
      El resto: se avisará
      Se avisará
      Póngase en contacto con el Servicio de Atención al Cliente
      Contact Customer Service

      		 Ampolla de plást. 100 mg
      Recuperando precio...
      No pudo obtenerse el precio
      La cantidad mínima tiene que ser múltiplo de
      Maximum Quantity is
      Al finalizar el pedido Más información
      Ahorró ()
       
      —
      Solicitar precio
      		 —
      Description
      OverviewA cell-permeable and irreversible antitumor and anti-inflammatory agent that acts as an inhibitor of 5-lipoxygenase (IC50 = 8 µM) and cyclooxygenase (IC50 = 52 µM). Confers significant protection against neurotoxic and genotoxic agents. Also inhibits the induction of nitric oxide synthase in activated macrophages (IC50 = 6 µM). Recently shown to inhibit the EGF receptor intrinsic kinase activity in the human epidermoid carcinoma A431 cells in a dose- and time-dependent manner. Also shown to be a p300/CREB-binding protein-specific inhibitor of histone acetyltransferase, inhibiting the acetylation of histones H3 and H4 with an IC50 of ~25 µM. Does not affect p300/CREB binding protein-associated factor (PCAF).
      Catalogue Number239802
      Brand Family Calbiochem®
      Synonyms1,7-Bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione, NOD2 Signaling Inhibitor I, Nucleotide-binding Oligomerization Domain 2 Signaling Inhibitor I, Histone Acetyltransferase Inhibitor I, HAT Inhibitor I, p300/CBP Inhibitor I
      References
      ReferencesHung, S., et al. 2008. Mol. Pharmacol. 74, 274.
      Cui, L., et al. 2007. Antimicrob. Agents Chemother. 51, 488.
      Salvioli, S., et al. 2007. eCAM 4, 181.
      Balasubramanyam, K. et al. 2004. J. Biol. Chem. 279, 51163.
      Brouet, I., and Okshima, H. 1995. Biochem. Biophys. Res. Commun. 206, 533.
      Korutla, L., and Kumar, R. 1994. Biochim. Biophys. Acta 1224, 597.
      Flynn, D.L., et al. 1986. Prostagland. Leuk. Med. 22, 357.
      Product Information
      CAS number458-37-7
      ATP CompetitiveN
      FormOrange-yellow solid
      Hill FormulaC₂₁H₂₀O₆
      Chemical formulaC₂₁H₂₀O₆
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary Target5-lipoxygenase
      Primary Target IC<sub>50</sub>8 µM, 52 µM, against 5-lipoxygenase, Cyclooxygenase, respectively; 6 µM inhibiting the induction of nitric oxide synthase in activated macrophages
      Purity≥80% by HPLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      RTECSMI5230000
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Standard Handling
      Storage +15°C to +30°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 3 months at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Número de referencia GTIN
      239802-100MG 04055977199581

      Documentation

      Curcumin, Curcuma longa L. - CAS 458-37-7 - Calbiochem Ficha datos de seguridad (MSDS)

      Título

      Ficha técnica de seguridad del material (MSDS) 

      Curcumin, Curcuma longa L. - CAS 458-37-7 - Calbiochem Certificados de análisis

      CargoNúmero de lote
      239802

      Referencias bibliográficas

      Visión general referencias
      Hung, S., et al. 2008. Mol. Pharmacol. 74, 274.
      Cui, L., et al. 2007. Antimicrob. Agents Chemother. 51, 488.
      Salvioli, S., et al. 2007. eCAM 4, 181.
      Balasubramanyam, K. et al. 2004. J. Biol. Chem. 279, 51163.
      Brouet, I., and Okshima, H. 1995. Biochem. Biophys. Res. Commun. 206, 533.
      Korutla, L., and Kumar, R. 1994. Biochim. Biophys. Acta 1224, 597.
      Flynn, D.L., et al. 1986. Prostagland. Leuk. Med. 22, 357.

      Folleto

      Cargo
      Alzheimer's Disease Brochure & Technical Guide

      Citas

      Título
    • Yuseok Moon, Wayne C. Glasgow and Thomas E. Eling. (2005) Curcumin suppresses interleukin 1β-mediated microsomal prostaglandin E synthase 1 (mPGES-1) by altering early growth response gene EGR-1 and other signaling pathways. Journal of Pharmacology and Experimental Therapeutics in press,.
      		•
      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.

      Revision28-April-2008 JSW
      Synonyms1,7-Bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione, NOD2 Signaling Inhibitor I, Nucleotide-binding Oligomerization Domain 2 Signaling Inhibitor I, Histone Acetyltransferase Inhibitor I, HAT Inhibitor I, p300/CBP Inhibitor I
      DescriptionA cell permeable antitumor and anti-inflammatory agent that acts as an inhibitor of 5-lipoxygenase (IC50 = 8 µM) and cyclooxygenase (IC50 = 52 µM). Confers significant protection against neurotoxic and genotoxic agents. Also inhibits the induction of nitric oxide synthase in activated macrophages (IC50 = 6 µM). Recently shown to inhibit the EGF receptor intrinsic kinase activity in the human epidermoid carcinoma A431 cells in a dose- and time-dependent manner. Also shown to be a p300/CREB-binding protein-specific inhibitor of histone acetyltransferase, inhibiting the acetylation of histones H3 and H4 with an
      IC50 of ~25 µM. Does not affect p300/CREB binding protein-associated factor (PCAF).
      FormOrange-yellow solid
      CAS number458-37-7
      RTECSMI5230000
      Chemical formulaC₂₁H₂₀O₆
      Structure formulaStructure formula
      Purity≥80% by HPLC
      SolubilityAcetic acid (10 mg/ml) or DMSO (5 mg/ml)
      Storage Protect from light
      +15°C to +30°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
      Toxicity Standard Handling
      Merck USA index14, 2673
      ReferencesHung, S., et al. 2008. Mol. Pharmacol. 74, 274.
      Cui, L., et al. 2007. Antimicrob. Agents Chemother. 51, 488.
      Salvioli, S., et al. 2007. eCAM 4, 181.
      Balasubramanyam, K. et al. 2004. J. Biol. Chem. 279, 51163.
      Brouet, I., and Okshima, H. 1995. Biochem. Biophys. Res. Commun. 206, 533.
      Korutla, L., and Kumar, R. 1994. Biochim. Biophys. Acta 1224, 597.
      Flynn, D.L., et al. 1986. Prostagland. Leuk. Med. 22, 357.
      Citation
    • Yuseok Moon, Wayne C. Glasgow and Thomas E. Eling. (2005) Curcumin suppresses interleukin 1β-mediated microsomal prostaglandin E synthase 1 (mPGES-1) by altering early growth response gene EGR-1 and other signaling pathways. Journal of Pharmacology and Experimental Therapeutics in press,.
      		•