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574102 Sulindac Sulfide - CAS 32004-67-4 - Calbiochem

A cell-permeable, active metabolite of Sulindac.

Sulindac Sulfide - CAS 32004-67-4 - 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: (Z)-5-Fluoro-2-methyl-1-[p-(methylthio)benzylidene]indene-3-acetic Acid

Primary Target: COX-1
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574102
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
32004-67-4C₂₀H₁₇FO₂S

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574102-5MGCN
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      		 樹脂ｱﾝﾌﾟﾙ 5 mg
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      Description
      OverviewA cell-permeable, active metabolite of Sulindac (Cat. No. 574100). Strongly inhibits Ras-induced malignant transformation and Ras/Raf-dependent transactivation. Also decreases the Ras-induced activation of c-Raf-1 kinase. Inhibits growth and induces apoptosis in prostate cancer cell lines. Selectively inhibits COX-1 (ID50 = 500 nM) compared to prostaglandin H synthase-2 (PGHS-2; COX-2; ID50 = 14 µM). Preferentially inhibits the secretion of Aβ42 in CHO cells stably transfected with both APP75, and the PS1 mutant M146L.
      Catalogue Number574102
      Brand Family Calbiochem®
      Synonyms(Z)-5-Fluoro-2-methyl-1-[p-(methylthio)benzylidene]indene-3-acetic Acid
      References
      ReferencesWeggen, S., et al. 2001. Nature 414, 212.
      Lim, J.T., et al. 1999. Biochem. Pharmacol. 58, 1097.
      Herrmann, C., et al. 1998. Oncogene 17, 1769.
      Picariello, L., et al. 1998. Eur. J. Pharmacol. 360, 105.
      Arber, N., et al. 1997. Gastroenterology 113, 1892.
      Meade, E.A., et al. 1993. J. Biol. Chem. 268, 6610.
      Product Information
      CAS number32004-67-4
      ATP CompetitiveN
      FormYellow-orange solid
      Hill FormulaC₂₀H₁₇FO₂S
      Chemical formulaC₂₀H₁₇FO₂S
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetCOX-1
      Primary Target IC<sub>50</sub>ID50 = 500 nM against COX-1
      Purity≥98% by TLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      R PhraseR: 22-42/43-63

      Harmful if swallowed.
      May cause sensitization by inhalation and skin contact.
      Possible risk of harm to the unborn child.
      S PhraseS: 36

      Wear suitable protective clothing.
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Harmful & Carcinogenic / Teratogenic
      Storage +15°C to +30°C
      Do not freeze Ok to freeze
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      574102-5MGCN 04055977189551

      Documentation

      Sulindac Sulfide - CAS 32004-67-4 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      Sulindac Sulfide - CAS 32004-67-4 - Calbiochem 試験成績書（CoA）

      タイトルロット番号
      574102

      参考資料

      参考資料の概要
      Weggen, S., et al. 2001. Nature 414, 212.
      Lim, J.T., et al. 1999. Biochem. Pharmacol. 58, 1097.
      Herrmann, C., et al. 1998. Oncogene 17, 1769.
      Picariello, L., et al. 1998. Eur. J. Pharmacol. 360, 105.
      Arber, N., et al. 1997. Gastroenterology 113, 1892.
      Meade, E.A., et al. 1993. J. Biol. Chem. 268, 6610.
      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.

      Revision12-September-2008 RFH
      Synonyms(Z)-5-Fluoro-2-methyl-1-[p-(methylthio)benzylidene]indene-3-acetic Acid
      DescriptionAn active metabolite of the non-steroidal anti-inflammatory drug Sulindac (Cat. No. 574100). Inhibits Ras signaling. Strongly inhibits Ras-induced malignant transformation and Ras/Raf-dependent transactivation. Also decreases the Ras-induced activation of c-Raf-1 kinase. Inhibits cell growth and induces apoptosis in a time-and dose-dependent manner. Selectively inhibits prostaglandin H synthase-1 (PGHS-1; COX-1; ID50 = 0.5 µM) relative to prostaglandin H synthase-2 (PGHS-2; COX-2; ID50 = 14 µM). Reduces Aβ42 production independently of COX inhibition.
      FormYellow-orange solid
      CAS number32004-67-4
      Chemical formulaC₂₀H₁₇FO₂S
      Structure formulaStructure formula
      Purity≥98% by TLC
      SolubilityDMSO (25 mg/ml) or ethanol (5 mg/ml)
      Storage +15°C to +30°C
      Do Not Freeze Ok to freeze
      Toxicity Harmful & Carcinogenic / Teratogenic
      ReferencesWeggen, S., et al. 2001. Nature 414, 212.
      Lim, J.T., et al. 1999. Biochem. Pharmacol. 58, 1097.
      Herrmann, C., et al. 1998. Oncogene 17, 1769.
      Picariello, L., et al. 1998. Eur. J. Pharmacol. 360, 105.
      Arber, N., et al. 1997. Gastroenterology 113, 1892.
      Meade, E.A., et al. 1993. J. Biol. Chem. 268, 6610.