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345834 Genistein, Soybean - CAS 446-72-0 - Calbiochem

A cell-permeable, reversible, substrate competitive inhibitor of protein tyrosine kinases, including autophosphorylation of epidermal growth factor receptor kinase (IC₅₀ = 2.6 µM).

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: 4ʹ,5,7-Trihydroxyisoflavone

Primary Target: EGFR kinase
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345834
가격 및 재고 조회

개요

Replacement Information

주요 사양표

CAS #Empirical Formula
446-72-0C₁₅H₁₀O₅

가격 및 재고여부

카탈로그 번호 재고 정보패킹 포장 단위 가격(VAT 별도) 수량
345834-20MGCN
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      		 Glass bottle 20 mg
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      345834-50MGCN
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          		 Plastic ampoule 50 mg
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          Description
          OverviewA cell-permeable, reversible, substrate competitive inhibitor of protein tyrosine kinases, including autophosphorylation of epidermal growth factor receptor kinase (IC50 = 2.6 µM). The inhibition is competitive with respect to ATP and non-competitive with respect to the phosphate acceptor. Has only a trivial effect on the activity of PKA and PKC (IC50 > 350 µM). Inhibits tumor cell proliferation and induces tumor cell differentiation. Produces cell cycle arrest and apoptosis in Jurkat T-leukemia cells. However, it prevents anti-CD3 monoclonal antibody-induced thymic apoptosis. Also inhibits topoisomerase II activity in vitro.
          Catalogue Number345834
          Brand Family Calbiochem®
          Synonyms4ʹ,5,7-Trihydroxyisoflavone
          References
          ReferencesConstantinou, A., and Huberman, E. 1995. Proc. Soc. Exp. Biol. Med. 208, 109.
          Wei, H., et al. 1995. Proc. Soc. Exp. Biol. Med. 208, 124.
          Wei, H., et al. 1995. Carcinogenesis 17, 73.
          Kobayashi, S., et al. 1994. J. Biol. Chem. 269, 9011.
          Migita, K., et al. 1994. J. Immunol. 153, 3457.
          Spinozzi, F., et al. 1994. Leuk. Res. 18, 431.
          Dhar, A., et al. 1990. Mol. Pharmacol. 37, 519.
          Hill, T.D., et al. 1990. Science 248, 1660.
          Dean, N.M., et al. 1989. Biochem. Biophys. Res. Commun. 165, 795.
          Akiyama, T., et al. 1987. J. Biol. Chem. 262, 5592.
          Product Information
          CAS number446-72-0
          ATP CompetitiveN
          FormWhite solid
          Hill FormulaC₁₅H₁₀O₅
          Chemical formulaC₁₅H₁₀O₅
          ReversibleY
          Structure formula ImageStructure formula Image
          Quality LevelMQ100
          Applications
          Biological Information
          Primary TargetEGFR kinase
          Primary Target IC<sub>50</sub>2.6 µM against autophosphorylation of epidermal growth factor receptor kinase
          Purity≥95% by HPLC
          Physicochemical Information
          Cell permeableY
          Dimensions
          Materials Information
          Toxicological Information
          Safety Information according to GHS
          RTECSNR2392000
          Safety Information
          Product Usage Statements
          Storage and Shipping Information
          Ship Code Ambient Temperature Only
          Toxicity Standard Handling
          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 6 months at -20°C.
          Packaging Information
          Transport Information
          Supplemental Information
          Specifications
          Global Trade Item Number
          카탈로그 번호 GTIN
          345834-20MGCN 04055977214376
          345834-50MGCN 04055977214383

          Documentation

          Genistein, Soybean - CAS 446-72-0 - Calbiochem MSDS

          타이틀

          물질안전보건자료(MSDS) 

          Genistein, Soybean - CAS 446-72-0 - Calbiochem Certificates of Analysis

          TitleLot Number
          345834

          References

          참고문헌 보기
          Constantinou, A., and Huberman, E. 1995. Proc. Soc. Exp. Biol. Med. 208, 109.
          Wei, H., et al. 1995. Proc. Soc. Exp. Biol. Med. 208, 124.
          Wei, H., et al. 1995. Carcinogenesis 17, 73.
          Kobayashi, S., et al. 1994. J. Biol. Chem. 269, 9011.
          Migita, K., et al. 1994. J. Immunol. 153, 3457.
          Spinozzi, F., et al. 1994. Leuk. Res. 18, 431.
          Dhar, A., et al. 1990. Mol. Pharmacol. 37, 519.
          Hill, T.D., et al. 1990. Science 248, 1660.
          Dean, N.M., et al. 1989. Biochem. Biophys. Res. Commun. 165, 795.
          Akiyama, T., et al. 1987. J. Biol. Chem. 262, 5592.

          Brochure

          Title
          Caspases and other Apoptosis Related Tools Brochure

          Citations

          타이틀
        • Weijian Shao, Roy C. Orlando and Mouhamed S. Awayda. (2005) Bisphosphonates stimulate an endogenous nonselective cation channel in Xenopus oocytes: potential mechanism of action. American Journal of Physiology Cell Physiology 289, C248-C256.
          		•
          Data Sheet

          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.

          Revision16-April-2010 JSW
          Synonyms4ʹ,5,7-Trihydroxyisoflavone
          DescriptionA cell-permeable, reversible, substrate competitive inhibitor of protein tyrosine kinases, including autophosphorylation of epidermal growth factor receptor kinase (IC50 = 2.6 µM). The inhibition is competitive with respect to ATP and non-competitive with respect to the phosphate acceptor. Inhibits tumor cell proliferation and induces tumor cell differentiation. Inhibits exogenous substrate phosphorylation by EGFR kinase and pp60v-src with similar potencies (IC50 = 20-25 µM). Has only a trivial effect on PKC and PKA (IC50 >350 µM). Produces cell cycle arrest and apoptosis in Jurkat T-leukemia cells. Prevents anti-CD3 monoclonal antibody-induced thymic apoptosis. Also inhibits topoisomerase II activity in vitro. Blocks oxidative DNA damage in vitro.
          FormWhite solid
          CAS number446-72-0
          RTECSNR2392000
          Chemical formulaC₁₅H₁₀O₅
          Structure formulaStructure formula
          Purity≥95% by HPLC
          SolubilityDMSO (200 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 6 months at -20°C.
          Toxicity Standard Handling
          Merck USA index14, 4391
          ReferencesConstantinou, A., and Huberman, E. 1995. Proc. Soc. Exp. Biol. Med. 208, 109.
          Wei, H., et al. 1995. Proc. Soc. Exp. Biol. Med. 208, 124.
          Wei, H., et al. 1995. Carcinogenesis 17, 73.
          Kobayashi, S., et al. 1994. J. Biol. Chem. 269, 9011.
          Migita, K., et al. 1994. J. Immunol. 153, 3457.
          Spinozzi, F., et al. 1994. Leuk. Res. 18, 431.
          Dhar, A., et al. 1990. Mol. Pharmacol. 37, 519.
          Hill, T.D., et al. 1990. Science 248, 1660.
          Dean, N.M., et al. 1989. Biochem. Biophys. Res. Commun. 165, 795.
          Akiyama, T., et al. 1987. J. Biol. Chem. 262, 5592.
          Citation
        • Weijian Shao, Roy C. Orlando and Mouhamed S. Awayda. (2005) Bisphosphonates stimulate an endogenous nonselective cation channel in Xenopus oocytes: potential mechanism of action. American Journal of Physiology Cell Physiology 289, C248-C256.
          		•