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532606 5-Lipoxygenase Inhibitor, MK591 - CAS 147030-01-1 - Calbiochem

MK591; MK0591; 5-LOX inhibitor, 5- Lipoxygenase inhibitor, FLAP

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

Synonymes: FLAP Inhibitor, MK591, sodium 3-(3-(tert-butylthio)-1-(4-chlorobenzyl)-5-(quinolin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethylpropanoate, L-686,708, MK-0591

Primary Target: FLAP
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532606
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Tableau de caractéristiques principal

CAS #Empirical Formula
147030-01-1C₃₄H₃₄ClN₂NaO₃S

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      Description
      OverviewA cell permeable, bioavailable, 2-indolealkanoic acid derived compound that acts as a highly potent and selective inhibitor of leukotriene biosynthesis (IC50 = 3.1 nM in intact human polymorphonuclear leukocytes). Shown to inhibit 5-lipoxygenase (5-LOX) activity in LNCaP prostate cancer cells by high-affinity binding to 5-lipoxygenase activating protein (FLAP; IC50 = 1.6 nM in a FLAP binding assay). Induces apoptosis in LNCaP cells without blocking PI 3 kinase-Akt or ERK activities. Also shown to induce rapid phosphorylation of c-Jun N-terminal Kinase (JNK) and indirectly block PKCε activity. Suppresses the deposition of Ab1-40 and Ab1-42 peptides in Tg2576 mice (~40 mg/kg/day in diet) with concomitant reduction in the levels of presenilin 1, nicastrin, APH-1 and Pen-2, but without affecting notch signaling. Exhibits desirable pharmacokinetic properties with tmax of 3.3 h and t1/2 = ~12 h.

      Please note that the molecular weight for this compound is batch-specific due to variable water content.
      Catalogue Number532606
      Brand Family Calbiochem®
      SynonymsFLAP Inhibitor, MK591, sodium 3-(3-(tert-butylthio)-1-(4-chlorobenzyl)-5-(quinolin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethylpropanoate, L-686,708, MK-0591
      References
      ReferencesChu, J., et al. 2012. J. Neuroinflamm. 9, 127.
      Sarveswaran, S., et al. 2011. Bioch. Biophy. Acta. 1813, 2108.
      Sarveswaran, S., et al. 2010. Cancer Lett. 291, 167.
      Uematsu, T., et al. 1995. Br. J. Clin. Pharm. 40, 59.
      Product Information
      CAS number147030-01-1
      FormWhite solid
      Hill FormulaC₃₄H₃₄ClN₂NaO₃S
      Chemical formulaC₃₄H₃₄ClN₂NaO₃S
      ReversibleY
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetFLAP
      Primary Target IC<sub>50</sub>3.1 nM
      Purity≥98% 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 Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
      Toxicity Standard Handling
      Storage -20°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
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Référence GTIN
      5326060001 04055977240948

      Documentation

      5-Lipoxygenase Inhibitor, MK591 - CAS 147030-01-1 - Calbiochem FDS

      Titre

      Fiche de données de sécurité des matériaux (FDS) 

      Références bibliographiques

      Aperçu de la référence bibliographique
      Chu, J., et al. 2012. J. Neuroinflamm. 9, 127.
      Sarveswaran, S., et al. 2011. Bioch. Biophy. Acta. 1813, 2108.
      Sarveswaran, S., et al. 2010. Cancer Lett. 291, 167.
      Uematsu, T., et al. 1995. Br. J. Clin. Pharm. 40, 59.

      Brochure

      Titre
      NPI Flyer- Epigenetics and Nuclear Function Feature
      New Products - Antibodies, Small Molecule, Inhibitors

      Informations techniques

      Titre
      White Paper: Further considerations of antibody validation and usage.
      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.

      Revision19-December-2014 JSW
      SynonymsFLAP Inhibitor, MK591, sodium 3-(3-(tert-butylthio)-1-(4-chlorobenzyl)-5-(quinolin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethylpropanoate, L-686,708, MK-0591
      DescriptionA cell permeable, bioavailable, 2-indolealkanoic acid derived compound that acts as a highly potent and selective inhibitor of leukotriene biosynthesis (IC50 = 3.1 nM in intact human polymorphonuclear leukocytes). Shown to inhibit 5-lipoxygenase (5-LOX) activity in LNCaP prostate cancer cells by high-affinity binding to 5-lipoxygenase activating protein (FLAP; IC50 = 1.6 nM in a FLAP binding assay). Induces apoptosis in LNCaP cells without blocking PI 3 kinase-Akt or ERK activities. Also shown to induce rapid phosphorylation of c-Jun N-terminal Kinase (JNK) and indirectly block PKCε activity. Suppresses the deposition of Ab1-40 and Ab1-42 peptides in Tg2576 mice (~40 mg/kg/day in diet) with concomitant reduction in the levels of presenilin 1, nicastrin, APH-1 and Pen-2, but without affecting notch signaling. Exhibits desirable pharmacokinetic properties with tmax of 3.3 h and t1/2 = ~12 h.
      FormWhite solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number147030-01-1
      Chemical formulaC₃₄H₃₄ClN₂NaO₃S
      Purity≥98% by HPLC
      SolubilityDMSO (10 mg/ml)
      Storage Protect from light
      -20°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
      ReferencesChu, J., et al. 2012. J. Neuroinflamm. 9, 127.
      Sarveswaran, S., et al. 2011. Bioch. Biophy. Acta. 1813, 2108.
      Sarveswaran, S., et al. 2010. Cancer Lett. 291, 167.
      Uematsu, T., et al. 1995. Br. J. Clin. Pharm. 40, 59.