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    Thapsigargin

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      Thapsigargin

      SKU
      T0284

      Category: Lipids, Fatty Acids

      67526-95-8
      CAS-Number
      C34H50O12
      Molecular Formula
      650.75
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Appearance
      White crystalline powder
      Identity
      1H-NMR

      Properties

      Solvents
      Soluble in methanol, ethanol or DMSO.
      Shipping
      AMBIENT
      Short Term Storage
      -20°C
      Long Term Storage
      -20°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at -20°C.
      Hazard statements
      H315 - H319 - H334 - H335
      Precautionary statements
      P261 - P264 - P271 - P302 + P352 - P304 + P340 + P312 - P305 + P351 + P338
      GHS Symbol
      GHS07+GHS08
      Signal word
      Danger
      Transportation
      Not dangerous goods
      Description
      Thapsigargin is a non-competitive, cell permeable inhibitor of calcium transport by SERCAs (IC50 values are cell type-dependent and range from ~2-80 nM). Inhibition of SERCAs leads to an increase in intracellular calcium, which has been linked to cell activation, release of histamine from mast cells, and increased proliferation of certain types of cancer cells. Thapsigargin shows anti-inflammatory and anti-cancer effects.
      Smiles
      O=C1OC2C3=C(C)[C@@H](OC(/C(C)=C\C)=O)[C@@H](OC(CCCCCCC)=O)[C@]3([H])[C@](C)(OC(C)=O)C[C@@H](OC(CCC)=O)[C@]2(O)[C@@]1(O)C
      InChi Key
      IXFPJGBNCFXKPI-IVRBKYRWSA-N
      References
      (1) S.A. Patkar, et al.; Agents Actions 9, 53 (1979) , (2) H. Hakii, et al., J. Cancer. Res. Clin. Oncol. 111, 177 (1986) , (3) Y. Sagara, & G. Inesi; J. Biol. Chem. 266, 13503 (1991) , (4) A. Tsukamoto & Y. Kaneko; Cell Biol. Int. 17, 969 (1993) , (5) J.P. Beaver & P. Waring; Cell Death Differ. 3, 415 (1996) , (6) M. Treiman, et al.; Trends Pharmacol. Sci. 19,131 (1998) , (7) B. Tombal, et al.; Prostate 43, 303 (2000) , (8) S.B. Christensen, et al.; Anticancer Agents Med. Chem. 9, 276 (2009) , (9) N.T. Quynh Doan & S.B. Christensen; Curr. Pharm. Des. 21, 5501 (2015) (Review) , (10) N.T. Doan, et al.; Steroids 97, 2 (2015) (Review) , (11) A. Jaskulska, et al.; Int. J. Mol. Sci. 22, 4 (2020) (Review)
      InChi
      (1) N.A. Kuznetsova et al.: Russ. J. Gen. Chem. 71, 36 (2001)

      Thapsigargin is a non-competitive, cell permeable inhibitor of calcium transport by SERCAs (IC50 values are cell type-dependent and range from ~2-80 nM). Inhibition of SERCAs leads to an increase in intracellular calcium, which has been linked to cell activation, release of histamine from mast cells, and increased proliferation of certain types of cancer cells. Thapsigargin shows anti-inflammatory and anti-cancer effects.

      Artikelnummer: T0284 Kategorie: Lipids, Fatty Acids
      • Zusätzliche Informationen

      Zusätzliche Informationen

      Purity

      ≥98% (HPLC)

      Appearance

      White crystalline powder

      CAS-Number

      67526-95-8

      Molecular Formula

      C34H50O12

      Molecular Weight

      650.75

      Identity

      1H-NMR

      Solvents

      Soluble in methanol, ethanol or DMSO.

      Smiles

      O=C1OC2C3=C(C)[C@@H](OC(/C(C)=C\C)=O)[C@@H](OC(CCCCCCC)=O)[C@]3([H])[C@](C)(OC(C)=O)C[C@@H](OC(CCC)=O)[C@]2(O)[C@@]1(O)C

      InChi Key

      IXFPJGBNCFXKPI-IVRBKYRWSA-N

      Shipping

      AMBIENT

      Short Term Storage

      -20°C

      Long Term Storage

      -20°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at -20°C.

      Hazard statements

      H315 – H319 – H334 – H335

      Precautionary statements

      P261 – P264 – P271 – P302 + P352 – P304 + P340 + P312 – P305 + P351 + P338

      GHS Symbol

      GHS07+GHS08

      Signal word

      Danger

      Transportation

      Not dangerous goods

      References

      (1) S.A. Patkar, et al.; Agents Actions 9, 53 (1979), (2) H. Hakii, et al., J. Cancer. Res. Clin. Oncol. 111, 177 (1986), (3) Y. Sagara, & G. Inesi; J. Biol. Chem. 266, 13503 (1991), (4) A. Tsukamoto & Y. Kaneko; Cell Biol. Int. 17, 969 (1993), (5) J.P. Beaver & P. Waring; Cell Death Differ. 3, 415 (1996), (6) M. Treiman, et al.; Trends Pharmacol. Sci. 19,131 (1998), (7) B. Tombal, et al.; Prostate 43, 303 (2000), (8) S.B. Christensen, et al.; Anticancer Agents Med. Chem. 9, 276 (2009), (9) N.T. Quynh Doan & S.B. Christensen; Curr. Pharm. Des. 21, 5501 (2015) (Review), (10) N.T. Doan, et al.; Steroids 97, 2 (2015) (Review), (11) A. Jaskulska, et al.; Int. J. Mol. Sci. 22, 4 (2020) (Review)

      InChi

      (1) N.A. Kuznetsova et al.: Russ. J. Gen. Chem. 71, 36 (2001)

      Quantity

      1 mg, 5 mg, Bulk

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