Millipore Sigma Vibrant Logo

215921 Chlorpromazine, Hydrochloride - CAS 69-09-0 - Calbiochem

Inhibits calmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase (IC₅₀ = 17 µM).

Chlorpromazine, Hydrochloride - CAS 69-09-0 - 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: 2-Chloro-10-[3ʹ-(dimethylamino)propyl]phenothiazine, HCl

Primary Target: Calmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase
View This Product on Sigma-Aldrich
215921
価格＆在庫状況を照会

概要

Replacement Information

主要スペック表

CAS #Empirical Formula
69-09-0C₁₇H₁₉ClN₂S · HCl

価格＆在庫状況

カタログ番号 在庫状況包装 Qty/Pk 価格 数量
215921-500MGCN
在庫状況検索中…
—
現在国内在庫なし 現在国内在庫なし
現在国内在庫有り 
販売中止
在庫僅少
現在国内在庫あり
    Remaining : Will advise
      Remaining : Will advise
      注文対象外
      お問合せください
      Contact Customer Service

      		 ｱﾙﾐﾆｳﾑｶﾝ 500 mg
      価格を検索中…
      価格が見つかりません
      Minimum Quantity needs to be mulitiple of
      Maximum Quantity is
      弊社照会 詳細を表示　
      値引
      ()
       
      —
      弊社照会
      		 —
      Description
      OverviewInhibits calmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase (IC50 = 17 µM). Acts as a peripheral vasodilator. Acts as an inhibitor of lysosomal sphingomyelinase and of TNF-α production. Inhibits nitric oxide synthase (NOS) in mouse brain and prevents lipopolysaccharide induction of NOS in murine lung. Shown to potently and specifically inhibit KSP/Eg5 (IC50 < 10 µM), and PLA2.
      Catalogue Number215921
      Brand Family Calbiochem®
      Synonyms2-Chloro-10-[3ʹ-(dimethylamino)propyl]phenothiazine, HCl
      References
      ReferencesLee, M.S., et al. 2007. Cancer Res. 67, 11359.
      Maor, I., et al. 1995. Arteriosclero. Thromb. Vasc. Biol. 15, 1378.
      Netea, M.G., et al. 1995. J. Infect. Dis. 171, 393.
      Lindahl, M., and Tagesson, C. 1993. Inflammation 17, 573.
      Palacios, M., et al. 1993. Biochem. Biophys. Res. Commun. 196, 280.
      Yamamoto, H. 1993. Toxicol. Lett. 66, 73.
      Vadas, P., et al. 1986. Agents Actions 19, 194.
      Marshak, P.R., et al. 1985. Biochemistry 24, 144.
      Product Information
      CAS number69-09-0
      ATP CompetitiveN
      FormOff-white crystalline solid
      Hill FormulaC₁₇H₁₉ClN₂S · HCl
      Chemical formulaC₁₇H₁₉ClN₂S · HCl
      Hygroscopic Hygroscopic
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetCalmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase
      Primary Target IC<sub>50</sub>17 µM inhibiting calmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase
      Purity≥99% by HPLC
      Physicochemical Information
      Cell permeableN
      ContaminantsHeavy metals: ≤0.002%; iron: ≤0.001%; sulfate: ≤0.05%
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      RTECSSO1750000
      Safety Information
      R PhraseR: 25-26-36/37/38

      Toxic if swallowed.
      Very toxic by inhalation.
      Irritating to eyes, respiratory system and skin.
      S PhraseS: 22-26-36/37/39-45

      Do not breathe dust.
      In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
      Wear suitable protective clothing, gloves and eye/face protection.
      In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Toxic
      Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
      Storage +15°C to +30°C
      Hygroscopic Hygroscopic
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze at -20°C. Stock solutions are stable for up to 6 months at -20°C and for up to 1 week at 4°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      215921-500MGCN 07790788048549

      Documentation

      Chlorpromazine, Hydrochloride - CAS 69-09-0 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      Chlorpromazine, Hydrochloride - CAS 69-09-0 - Calbiochem 試験成績書（CoA）

      タイトルロット番号
      215921

      参考資料

      参考資料の概要
      Lee, M.S., et al. 2007. Cancer Res. 67, 11359.
      Maor, I., et al. 1995. Arteriosclero. Thromb. Vasc. Biol. 15, 1378.
      Netea, M.G., et al. 1995. J. Infect. Dis. 171, 393.
      Lindahl, M., and Tagesson, C. 1993. Inflammation 17, 573.
      Palacios, M., et al. 1993. Biochem. Biophys. Res. Commun. 196, 280.
      Yamamoto, H. 1993. Toxicol. Lett. 66, 73.
      Vadas, P., et al. 1986. Agents Actions 19, 194.
      Marshak, P.R., et al. 1985. Biochemistry 24, 144.
      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.

      Revision25-April-2018 JSW
      Synonyms2-Chloro-10-[3ʹ-(dimethylamino)propyl]phenothiazine, HCl
      DescriptionInhibits calmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase (IC50 = 17 µM). Acts as a peripheral vasodilator. An inhibitor of TNFα production. Inhibits nitric oxide synthase (NOS) in mouse brain and prevents lipopolysaccharide induction of NOS in murine lung. Shown to potently and specifically inhibit KSP/Eg5 (IC50 < 10 µM), and PLA2.
      FormOff-white crystalline solid
      CAS number69-09-0
      RTECSSO1750000
      Chemical formulaC₁₇H₁₉ClN₂S · HCl
      Structure formulaStructure formula
      Purity≥99% by HPLC
      ContaminantsHeavy metals: ≤0.002%; iron: ≤0.001%; sulfate: ≤0.05%
      SolubilityH₂O (50 mg/ml) or Methanol (10 mg/ml)
      Storage +15°C to +30°C
      Hygroscopic
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze at -20°C. Stock solutions are stable for up to 6 months at -20°C and for up to 1 week at 4°C.
      Toxicity Toxic
      Merck USA index14, 2185
      ReferencesLee, M.S., et al. 2007. Cancer Res. 67, 11359.
      Maor, I., et al. 1995. Arteriosclero. Thromb. Vasc. Biol. 15, 1378.
      Netea, M.G., et al. 1995. J. Infect. Dis. 171, 393.
      Lindahl, M., and Tagesson, C. 1993. Inflammation 17, 573.
      Palacios, M., et al. 1993. Biochem. Biophys. Res. Commun. 196, 280.
      Yamamoto, H. 1993. Toxicol. Lett. 66, 73.
      Vadas, P., et al. 1986. Agents Actions 19, 194.
      Marshak, P.R., et al. 1985. Biochemistry 24, 144.

      関連製品＆アプリケーション

      カテゴリー

      Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Lipid Signaling Inhibitors > Sphingomyelinase Kinase Inhibitors
      Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Other Inhibitors of Biological Interest > Phosphodiesterase Inhibitors
      Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Nitric Oxide and Oxidative Stress > Nitric Oxide Synthase (NOS) Inhibitors