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

BQ-788, Sodium Salt - CAS - 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: N-cis-2,6-Dimethylpiperidinocarbonyl-L-γ-MeLeu-D-Trp(MeOCO)-D-Nle-OH, Na

Primary Target: ETB-receptor antagonist
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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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      		 樹脂ｱﾝﾌﾟﾙ 1 mg
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      05-22-3838-5MGCN
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          		 樹脂ｱﾝﾌﾟﾙ 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
          Quality LevelMQ100
          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
          Global Trade Item Number
          カタログ番号 GTIN
          05-22-3838-1MGCN 04055977225051
          05-22-3838-5MGCN 04055977225068

          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 Protect from moisture
          -20°C
          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.