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534377 CMB-087229 - CAS 1227692-67-2 - Calbiochem

CMB-087229 - CAS 1227692-67-2 - Calbiochem: のSDS（安全データシート）、CoA（試験成績書）およびCoQ（品質証明書）、カタログなど製品関連の技術資料を入手いただけます。

同義語: 5-[(3,5-Dichlorophenoxy)methyl]-1,2-dihydro-3H-pyrazol-3-one, CMB087229

Primary Target: 26S proteasome PSMC1 and PSMC4 and the chaperone protein TCP-1
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534377
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
1227692-67-2C₁₀H₈Cl₂N₂O₂

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      		 ｶﾞﾗｽﾋﾞﾝ 25 mg
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      Description
      OverviewA cell-permeable, blood-brain barrier permeable, non-toxic pyrazolone compound that potently blocks mutant Cu/Zn SOD1 cytotoxicity (EC50 = 67 nM in PC12 cells expressing mutant G93A SOD1). Shown to directly interact with 26S proteasome PSMC1 and PSMC4 and the chaperone protein TCP-1 and enhance proteasome activity. Offers neuroprotection against protein aggregation induced toxicity and prolongs the survival of ALS transgenic mice by 13.3% (20 mg/kg, i.p., q.d.) Demonstrates attractive microsomal (T1/2 = 93 & 36 min in human & mouse, respectively) and metabolic stability, aqueous solubility (250 µM) and PK profile in mice. Poorly affects the activities of 68-enzymes & receptors, hERG and Cyp450 isozymes at 10 µM.

      Please note that the molecular weight for this compound is batch-specific due to variable water content. Please refer to the vial label or the certificate of analysis for the batch-specific molecular weight. The molecular weight provided represents the baseline molecular weight without water.
      Catalogue Number534377
      Brand Family Calbiochem®
      Synonyms5-[(3,5-Dichlorophenoxy)methyl]-1,2-dihydro-3H-pyrazol-3-one, CMB087229
      References
      ReferencesTripper, P.C., et al. 2014. ACS Chem. Neurosci. 5, 823.
      Chen, T., et al. 2012. J. Med. Chem. 55, 515.
      Product Information
      CAS number1227692-67-2
      FormWhite solid
      Hill FormulaC₁₀H₈Cl₂N₂O₂
      Chemical formulaC₁₀H₈Cl₂N₂O₂
      ReversibleY
      Quality LevelMQ100
      Applications
      Biological Information
      Primary Target26S proteasome PSMC1 and PSMC4 and the chaperone protein TCP-1
      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 Ambient Temperature Only
      Toxicity Standard Handling
      Storage +2°C to +8°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
      カタログ番号 GTIN
      5.34377.0001 04054839117176

      Documentation

      CMB-087229 - CAS 1227692-67-2 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      CMB-087229 - CAS 1227692-67-2 - Calbiochem 試験成績書（CoA）

      タイトルロット番号
      534377

      参考資料

      参考資料の概要
      Tripper, P.C., et al. 2014. ACS Chem. Neurosci. 5, 823.
      Chen, T., et al. 2012. J. Med. Chem. 55, 515.
      データシート

      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-July-2017 JSW
      Synonyms5-[(3,5-Dichlorophenoxy)methyl]-1,2-dihydro-3H-pyrazol-3-one, CMB087229
      DescriptionA cell-permeable, blood-brain barrier permeable, non-toxic pyrazolone compound that potently blocks mutant Cu/Zn SOD1 cytotoxicity (EC50 = 67 nM in PC12 cells expressing mutant G93A SOD1). Shown to directly interact with 26S proteasome PSMC1 and PSMC4 and the chaperone protein TCP-1 and enhance proteasome activity. Offers neuroprotection against protein aggregation induced toxicity and prolongs the survival of ALS transgenic mice by 13.3% (20 mg/kg, i.p., q.d.) Demonstrates attractive microsomal (T1/2 = 93 & 36 min in human & mouse, respectively) and metabolic stability, aqueous solubility (250 µM) and PK profile in mice. Poorly affects the activities of 68-enzymes & receptors, hERG and Cyp450 isozymes at 10 µM.
      FormWhite solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number1227692-67-2
      Chemical formulaC₁₀H₈Cl₂N₂O₂
      Purity≥98% by HPLC
      SolubilityDMSO (50 mg/ml)
      Storage Protect from light
      +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 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesTripper, P.C., et al. 2014. ACS Chem. Neurosci. 5, 823.
      Chen, T., et al. 2012. J. Med. Chem. 55, 515.