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239804 Cyclopamine-KAAD - Calbiochem

概述

Replacement Information

重要规格表

Empirical Formula
C₄₄H₆₃N₃O₄

价格及供货情况

产品目录编号 库存情况包装 数量 / 包装 价格 数量
239804-100UGCN
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      玻璃瓶 100 μg
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      239804-500UGCN
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          玻璃瓶 500 μg
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          Description
          OverviewA potent, cell-permeable analog of Cyclopamine (Cat. No. 239803) that specifically inhibits the Hedgehog (Hh) signaling with similar or lower toxicity (IC50 = 20 nM in Shh-LIGHT2 assay; 50 nM in p2Ptch-/-cells; 500 nM in SmoA1-LIGHT cells). Binds to SmoA1 and promotes its exit from the endoplasmic reticulum. Suppresses both the ShhNp-induced pathway activity and SmoA1-induced reporter activity. Shown to sensitize human glioma cells to TRAIL-induced apoptosis. Also available as a 1 mM solution in DMSO (Cat. No. 239807).
          Catalogue Number239804
          Brand Family Calbiochem®
          Synonyms3-Keto-N-(aminoethyl-aminocaproyl-dihydrocinnamoyl)cyclopamine, KAAD-Cyclopamine, Shh Signaling Antagonist II
          References
          ReferencesSiegelin, M.D. et al. 2009. Neurobiol. Dis. 34, 259.
          Watkins, D.N., et al. 2003. Nature 422, 313.
          Berman, D.M., et al. 2002. Science 297, 1559.
          Chen, J.K., et al. 2002. Proc. Natl. Acad. Sci. USA 99, 14071.
          Chen, J.K., et al. 2002. Genes Dev. 16, 2743.
          Frank-Kamenetsky, M., et al. 2002. J. Biol. 1, 10.
          Taipale, J., et al. 2000. Nature 406, 1005.
          Product Information
          ATP CompetitiveN
          FormWhite to light yellow solid
          Hill FormulaC₄₄H₆₃N₃O₄
          Chemical formulaC₄₄H₆₃N₃O₄
          ReversibleN
          Structure formula ImageStructure formula Image
          Quality LevelMQ100
          Applications
          Biological Information
          Primary TargetHh signaling in Shh-light2 assay
          Primary Target IC<sub>50</sub>20 nM against Hedgehog (Hh) signaling in Shh-LIGHT2 assay; 50 nM in p2Ptch-/-cells; 500 nM in SmoA1-LIGHT cells
          Purity≥70% by HPLC (sum of two isomers)
          Physicochemical Information
          Cell permeableY
          Dimensions
          Materials Information
          Toxicological Information
          Safety Information according to GHS
          Safety Information
          R PhraseR: 20/21/22

          Harmful by inhalation, in contact with skin and if swallowed.
          S PhraseS: 22-36/37

          Do not breathe dust.
          Wear suitable protective clothing and gloves.
          Product Usage Statements
          Storage and Shipping Information
          Ship Code Shipped with Blue Ice or with Dry Ice
          Toxicity Harmful
          Storage -20°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 2 weeks at -20°C.
          Packaging Information
          Packaged under inert gas Packaged under inert gas
          Transport Information
          Supplemental Information
          Specifications
          Global Trade Item Number
          产品目录编号 GTIN
          239804-100UGCN 04055977198881
          239804-500UGCN 04055977198898

          Documentation

          Cyclopamine-KAAD - Calbiochem MSDS

          职位

          物料安全数据表 (MSDS) 

          Cyclopamine-KAAD - Calbiochem 分析证书

          标题批号
          239804

          参考

          参考信息概述
          Siegelin, M.D. et al. 2009. Neurobiol. Dis. 34, 259.
          Watkins, D.N., et al. 2003. Nature 422, 313.
          Berman, D.M., et al. 2002. Science 297, 1559.
          Chen, J.K., et al. 2002. Proc. Natl. Acad. Sci. USA 99, 14071.
          Chen, J.K., et al. 2002. Genes Dev. 16, 2743.
          Frank-Kamenetsky, M., et al. 2002. J. Biol. 1, 10.
          Taipale, J., et al. 2000. Nature 406, 1005.

          数据表

          标题
          Reprogramming Cell Fate and Function Novel Strategies for iPSC Generation, Characterization, and Differentiation

          引用

          标题
        • Siegelin, M.D. et al. 2009. Neurobiol. Dis. 34, 259.
        • 数据表

          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.

          Revision23-October-2024 JSW
          Synonyms3-Keto-N-(aminoethyl-aminocaproyl-dihydrocinnamoyl)cyclopamine, KAAD-Cyclopamine, Shh Signaling Antagonist II
          DescriptionA cell-permeable potent analog of Cyclopamine (Cat. No. 239803) that specifically inhibits Hedgehog (Hh) signaling with similar or lower toxicity (IC50 = 20 nM in Shh-LIGHT2 assay; 50 nM in p2Ptch-/-cells; 500 nM in SmoA1-LIGHT cells). Binds to SmoA1 and promotes its exit from the endoplasmic reticulum. Suppresses both ShhNp-induced pathway activity and SmoA1-induced reporter activity. Reported to cause regression of murine tumor allografts in vivo and induce rapid cell death in human medulloblastoma. Shown to sensitize human glioma cells to TRAIL-induced apoptosis.
          FormWhite to light yellow solid
          Intert gas (Yes/No) Packaged under inert gas
          Chemical formulaC₄₄H₆₃N₃O₄
          Structure formulaStructure formula
          Purity≥70% by HPLC (sum of two isomers)
          SolubilityDMSO (5 mg/ml), Ethanol (1 mg/ml), or Methanol (1 mg/ml)
          Storage Protect from light
          -20°C
          Do Not Freeze Ok to freeze
          Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 2 weeks at -20°C.
          Toxicity Harmful
          ReferencesSiegelin, M.D. et al. 2009. Neurobiol. Dis. 34, 259.
          Watkins, D.N., et al. 2003. Nature 422, 313.
          Berman, D.M., et al. 2002. Science 297, 1559.
          Chen, J.K., et al. 2002. Proc. Natl. Acad. Sci. USA 99, 14071.
          Chen, J.K., et al. 2002. Genes Dev. 16, 2743.
          Frank-Kamenetsky, M., et al. 2002. J. Biol. 1, 10.
          Taipale, J., et al. 2000. Nature 406, 1005.
          Citation
        • Siegelin, M.D. et al. 2009. Neurobiol. Dis. 34, 259.