05-22-3838 BQ-788, Sodium Salt - CAS - Calbiochem

05-22-3838
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      概要

      Replacement Information

      主要スペック表

      Empirical Formula
      C₃₄H₅₀N₅O₇Na

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      カタログ番号在庫状況 包装 Qty/Pk 価格 数量
      05-22-3838-1MGCN
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          樹脂アンプル 1 mg
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          05-22-3838-5MGCN
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              樹脂アンプル 5 mg
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              Description
              OverviewHighly selective ETB-receptor antagonist (IC50 = 1.2 nM).
              Catalogue Number05-22-3838
              Brand Family Calbiochem®
              SynonymsN-cis-2,6-Dimethylpiperidinocarbonyl-L-γ-MeLeu-D-Trp(MeOCO)-D-Nle-OH, Na
              References
              ReferencesOkada, M., and Nishikibe, M. 2002. Cardiovasc. Drug Reviews 20, 53.
              Taniai, H., et al. 2001. Hepatology 33, 894.
              Fukuroda, T., et al. 1994. Biochem. Biophys. Res. Commun. 199, 1461.
              Ishikawa, K., et al. 1994. Proc. Natl. Acad. Sci. USA 91, 4892.
              Product Information
              ATP CompetitiveN
              FormWhite to off-white lyophilized solid
              Hill FormulaC₃₄H₅₀N₅O₇Na
              Chemical formulaC₃₄H₅₀N₅O₇Na
              ReversibleN
              Structure formula ImageStructure formula Image
              Applications
              Biological Information
              Primary TargetETB-receptor antagonist
              Primary Target IC<sub>50</sub>1.2 nM as ETB-receptor antagonist
              Purity≥95% by HPLC
              Physicochemical Information
              Cell permeableN
              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 -20°C
              Protect from Moisture Protect from moisture
              Do not freeze Ok to freeze
              Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). DMSO and Methano:H₂O stock solutions are stable for up to 2 months at -20°C.
              Packaging Information
              Transport Information
              Supplemental Information
              Specifications

              Documentation

              BQ-788, Sodium Salt - CAS - Calbiochem (M)SDS

              タイトル

              英語版製品安全データシート((M)SDS) 

              BQ-788, Sodium Salt - CAS - Calbiochem 試験成績書(CoA)

              タイトルロット番号
              05-22-3838

              参考資料

              参考資料の概要
              Okada, M., and Nishikibe, M. 2002. Cardiovasc. Drug Reviews 20, 53.
              Taniai, H., et al. 2001. Hepatology 33, 894.
              Fukuroda, T., et al. 1994. Biochem. Biophys. Res. Commun. 199, 1461.
              Ishikawa, K., et al. 1994. Proc. Natl. Acad. Sci. USA 91, 4892.
              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.

              Revision18-September-2008 RFH
              SynonymsN-cis-2,6-Dimethylpiperidinocarbonyl-L-γ-MeLeu-D-Trp(MeOCO)-D-Nle-OH, Na
              DescriptionA highly selective and competitive ETB receptor antagonist (IC50 = 1.2 nM).
              FormWhite to off-white lyophilized solid
              Chemical formulaC₃₄H₅₀N₅O₇Na
              Structure formulaStructure formula
              Purity≥95% by HPLC
              SolubilityDMSO (2 mg/ml), Methanol:H₂O (3:1) (2 mg/ml), or 0.01% NH₄OH (1 mg/ml)
              Storage -20°C
              Protect from moisture
              Do Not Freeze Ok to freeze
              Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). DMSO and Methano:H₂O stock solutions are stable for up to 2 months at -20°C.
              Toxicity Standard Handling
              ReferencesOkada, M., and Nishikibe, M. 2002. Cardiovasc. Drug Reviews 20, 53.
              Taniai, H., et al. 2001. Hepatology 33, 894.
              Fukuroda, T., et al. 1994. Biochem. Biophys. Res. Commun. 199, 1461.
              Ishikawa, K., et al. 1994. Proc. Natl. Acad. Sci. USA 91, 4892.