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    Ecdysterone

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      Ecdysterone

      SKU
      E0225

      Category: Steroids

      Synonyms
      20-Hydroxyecdysone , β-Ecdysone , 2β,3β,14α,20β,22,25-Hexahydroxy-7-cholesten-6-one , Insect moulting hormone , Polypodine A
      5289-74-7
      CAS-Number
      C27H44O7
      Molecular Formula
      480.63
      Molecular Weight

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

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥97% (HPLC)
      Appearance
      White to off-white powder
      Identity
      1H-NMR

      Properties

      Solvents
      methanol (20 mg/ml), DMSO, ethanol
      Shipping
      AMBIENT
      Short Term Storage
      +4°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.
      Transportation
      Not dangerous goods
      Description
      A member of the ecdysteroid family. Ecdysone receptor (EcR) agonist. More potent than ecdysone. Induces the expression of genes coding for proteins that the larva requires, and it causes chromosome puffs (sites of high expression) to form in polytene chromosomes. Plays a key role in insect development, cell proliferaton, growth and apoptosis by controlling gene expression involved in moulting and metamorphosis. It acts through a heterodimeric receptor comprising the ecdysone receptor and the ultraspiracle proteins (USP). Used for controlled gene expression in scientific research, agriculture and medicine. Used for the development of selective insect growth regulators for use as environmentally benign insecticides. Shows biological effects on mammalian species, including antiepileptic, antidiabetic, antiobesity, ROS-inhibiting activity.
      Smiles
      [H][C@@]1(CC[C@@]2(O)C3=CC(=O)[C@]4([H])C[C@@H](O)[C@@H](O)C[C@]4(C)C3CC[C@]12C)[C@@](C)(O)[C@H](O)CCC(C)(C)O
      InChi Key
      NKDFYOWSKOHCCO-MQMWGCQISA-N
      References
      (1) F. Engelmann, Science 174, 1041 (1971) , (2) S. Tsujiyama, et al., Jpn. J. Pharmacol. 68, 133 (1995) , (3) E.H. Baehrecke, et al., Arch. Insect Biochem. Physiol. 33, 231 (1996) , (4) R. Hanaya, et al., Jpn. J. Pharmacol. 74, 331 (1997) , (5) L.M. Riddiford, et al., Vitam. Horm. 60, 1 (2000) , (6) C.S Thummel, Insect Biochem. Mol. Biol. 32, 113 (2002) , (7) L.D. Graham, Expert Opin. Biol. Ther. 2, 525 (2002) , (8) P. Kizelsztein, et al., Am. J. Physiol. Endocrinol. Metab. 296, E433 (2009) , (9) J. Hu, et al., J. Cell Biochem. 111, 1512 (2010)
      InChi
      InChI=1S/C27H44O7/c1-23(2,32)9-8-22(31)26(5,33)21-7-11-27(34)16-12-18(28)17-13-19(29)20(30)14-24(17,3)15(16)6-10-25(21,27)4/h12,15,17,19-22,29-34H,6-11,13-14H2,1-5H3/t15?,17-,19+,20-,21-,22+,24+,25+,26+,27+/m0/s1

      A member of the ecdysteroid family. Ecdysone receptor (EcR) agonist. More potent than ecdysone. Induces the expression of genes coding for proteins that the larva requires, and it causes chromosome puffs (sites of high expression) to form in polytene chromosomes. Plays a key role in insect development, cell proliferaton, growth and apoptosis by controlling gene expression involved in moulting and metamorphosis. It acts through a heterodimeric receptor comprising the ecdysone receptor and the ultraspiracle proteins (USP). Used for controlled gene expression in scientific research, agriculture and medicine. Used for the development of selective insect growth regulators for use as environmentally benign insecticides. Shows biological effects on mammalian species, including antiepileptic, antidiabetic, antiobesity, ROS-inhibiting activity.

      SKU: E0225 Category: Steroids
      • Additional information

      Additional information

      Synonyms

      20-Hydroxyecdysone, β-Ecdysone, 2β,3β,14α,20β,22,25-Hexahydroxy-7-cholesten-6-one, Insect moulting hormone, Polypodine A

      Purity

      ≥97% (HPLC)

      Appearance

      White to off-white powder

      CAS-Number

      5289-74-7

      Molecular Formula

      C27H44O7

      Molecular Weight

      480.63

      Identity

      1H-NMR

      Solvents

      methanol (20 mg/ml), DMSO, ethanol

      Smiles

      [H][C@@]1(CC[C@@]2(O)C3=CC(=O)[C@]4([H])C[C@@H](O)[C@@H](O)C[C@]4(C)C3CC[C@]12C)[C@@](C)(O)[C@H](O)CCC(C)(C)O

      InChi Key

      NKDFYOWSKOHCCO-MQMWGCQISA-N

      Shipping

      AMBIENT

      Short Term Storage

      +4°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.

      Transportation

      Not dangerous goods

      References

      (1) F. Engelmann, Science 174, 1041 (1971), (2) S. Tsujiyama, et al., Jpn. J. Pharmacol. 68, 133 (1995), (3) E.H. Baehrecke, et al., Arch. Insect Biochem. Physiol. 33, 231 (1996), (4) R. Hanaya, et al., Jpn. J. Pharmacol. 74, 331 (1997), (5) L.M. Riddiford, et al., Vitam. Horm. 60, 1 (2000), (6) C.S Thummel, Insect Biochem. Mol. Biol. 32, 113 (2002), (7) L.D. Graham, Expert Opin. Biol. Ther. 2, 525 (2002), (8) P. Kizelsztein, et al., Am. J. Physiol. Endocrinol. Metab. 296, E433 (2009), (9) J. Hu, et al., J. Cell Biochem. 111, 1512 (2010)

      InChi

      InChI=1S/C27H44O7/c1-23(2,32)9-8-22(31)26(5,33)21-7-11-27(34)16-12-18(28)17-13-19(29)20(30)14-24(17,3)15(16)6-10-25(21,27)4/h12,15,17,19-22,29-34H,6-11,13-14H2,1-5H3/t15?,17-,19+,20-,21-,22+,24+,25+,26+,27+/m0/s1

      Quantity

      5 mg, 25 mg, Bulk

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