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Detail of "35399-32-7"

  • CAS Number:
  • 35399-32-7
  • Name:
  • 4H-1-Benzopyran-4-one,3-(b-D-galactopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-6,7-dimethoxy-

  • Superlist Name:
  • Betuletrin
  • Molecular Structure:
  • Formula:
  • C23H24O12
  • Deleted CAS:
  • 98604-37-6, 128450-83-9
  • Synonyms:
  • Betuletrin;Eupalitin3-O-galactoside;

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CAS No.35399-32-7 Betuletrin

Assay:98%  Appearance:powder or cr...  Package:10mg,20mg,1g...Storage:-20degree  Transportation:room tempera...  Application:For research...

Supplier:shanghai Tauto Biotech Co., Ltd [ China (Mainland)]

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Tel:+86-21-51320588 ext. 8025

Address:No. 326, Aidisheng Rd , Zhangjiang Hi-tech Park, Shanghai , P.R.CHINA

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CAS No.35399-32-7 Betuletrin

Registry number 35399-32-7 Molecular Formula C23H24O12 Molecular weight 492.43636 10 mg

Supplier:PhytoLab GmbH & Co. KG [ Germany]

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Tel:+49-9163-88327

Address:Dutendorfer Str. 5-7 91487 Vestenbergsgreuth GERMANY

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Reference

Effects on Cultured Neonatal Mouse Calvaria of the Flavonoids Isolated from Boerhaavia repens
Effects on Cultured Neonatal Mouse Calvaria of the Flavonoids Isolated from Boerhaavia repens. Li, Jianxin; Li, Huiying; Kadota, Shigetoshi; Namba, Tsuneo; Miyahara, Tatsurou; Khan, Usman Ghani (Research Institute for Wakan-Yaku (Traditional Sino-Japanese Medicines), Toyama Medical and Pharmaceutical University, Toyama 930-01, Japan). Journal of Natural Products, 59(11), 1015-1018 (English) 1996 American Chemical Society. CODEN: JNPRDF. ISSN: 0163-3864. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Section cross-reference(s): 11 A MeOH ext. from the whole plant of Boerhaavia repens was found to inhibit bone resorption induced by parathyroid hormone (PTH) in tissue culture. Systematic sepn. of the MeOH ext. 90706-64-2 and 35399-32-7 which are cas registry numbers are also used here. afforded one new and two known flavonoid glycosides, namely, eupalitin 3-O-b-D-galactopyranosyl-(1?2)-b-D-glucopyranoside (I), eupalitin 3-O-b-D-galactopyranoside(II), and 6-methoxykaempferol 3-O-b-D-(1?6)-robinoside. The structure of the new compd. I was detd. using spectroscopic techniques. The inhibitory activity of these substances toward bone resorption induced by PTH was evaluated, and compds. I and II were found to exhibit significant activity. .
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