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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
Contained glycoepitopes: IEDB_136044,IEDB_137472,IEDB_141794,IEDB_190606,SB_165,SB_166,SB_187,SB_195,SB_7,SB_88

• Article ID: 9206
  Servettaz O, Colombo ML, De Bernardi M, Uberti E, Vidari G, Vita-Finzi P "Flavonol glycosides from Dryas octopetala" - Journal of Natural Products 47(5) (1984) 809-814
  

  Six flavonol glycosides and ent-epicatechin were isolated from Dryas octopetala and their structures elucidated by chemical and spectroscopic methods. Two new flavonoids, 3-O-α-L-arabinofuranosyl-8-methoxyquercetin (2) and 3-O-β-galactopyranosyl-8-methoxykaempferol (6), were identified along with 3-O-β-D-galactopyranosylquercetin (hyperin) (3), 3-O-α-L-arabinofuranosylquercetin (avicularin) (5), 3-O-β-L-arabinopyranosylquercetin (4), and 3-O-β-D-galactopyranosyl-8-methoxyquercetin (1).

  flavonol glycosides, Dryas octopetala

  NCBI PubMed ID: 6512533
  Publication DOI: 10.1021/np50035a009
  Journal NLM ID: 7906882
  Publisher: American Society of Pharmacognosy
  Institutions: Dipartimento di Biología, Università di Milano, Milano, Italy, Istituto di Farmacologia e Farmacognosia, Università di Milano, Milano, Italy, Dipartimento di Chimica Organica, Università di Pavia, Pavia, Italy
  Methods: 1H NMR, EI-MS, methylation, IR, TLC, acid hydrolysis, GC, extraction, optical rotation measurement, acetylation, CC, RP-HPLC, melting point determination, derivatization, evaporation
  
   
  
  Dryas octopetala
  CSDB ID 50542 (all data & tools)

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Structure type: oligomer
Trivial name: sexangularetin‐3‐O‐yl β‐D‐sophoroside
Compound class: glycoside, flavonoid glycoside
Contained glycoepitopes: IEDB_140628,IEDB_142488,IEDB_146664,IEDB_983931,SB_192

• Article ID: 11037
  Stošić D, Gorunović M, Skaltsounis AL, Tillequin F, Koch M "New flavonoid glycosides from Paeonia tenuifolia L [French]" - Helvetica Chimica Acta 71(2) (1988) 348-353
  

  Two novel flavonoid glycosides have been isolated from the stamens of Paeonia tenuifolia, sexangularetin‐3‐O‐yl β‐D‐sophoroside (1) and limocitrin‐3‐O‐yl β‐D‐sophoroside (3). Their structures have been elucidated by spectroscopic means, mainly desorption chemical ionisation mass spectrometry and ID and 2D high‐resolution 1H‐NMR spectroscopy of their acety1 derivatives.

  Publication DOI: 10.1002/hlca.19880710207
  Journal NLM ID: 2985094R
  Publisher: Verlag Helvetica Chimica Acta
  Institutions: Institut de Pharmacognosie, Faculte de Pharmacie, Beograd, Serbia, Departement de Pharmacognosie de l'Universite Rene Descartes, Faculte des Sciences Pharmaceutiques et Biologiques, Paris, France
  Methods: 13C NMR, 1H NMR, MS, UV, acetylation, hydrolysis
  
   
  
  Paeonia, Paeonia tenuifolia
  CSDB ID 179510 (all data & tools)
• Article ID: 12372
  Ito H, Nishitani E, Konoshima T, Takasaki M, Kozuka M, Yoshida T "Flavonoid and benzophenone glycosides from Coleogyne ramosissima" - Phytochemistry 54(7) (2000) 695-700
  

  A benzophenone glucoside and two flavonol glycosides were isolated together with 27 known polyphenols from the aerial parts of Coleogyne ramosissima, and their structures were elucidated by spectroscopic and chemical methods as iriflophenone 2-O-β-glucopyranoside, isorhamnetin 3-O-2G-rhamnopyranosylrutinoside-7-O-α-rhamnopyranoside and limocitrin 3-O-rutinoside-7-O-β-glucopyranoside, respectively.

  rosaceae, Coleogyne ramosissima, iriflophenone 2-O-glucopyranoside, isorhamnetin 3-O-2G-rhamnopyranosylrutinoside-7-O-rhamnopyranoside, limocitrin 3-O-rutinoside-7-O-glucopyranoside

  NCBI PubMed ID: 10975504
  Publication DOI: 10.1016/s0031-9422(00)00192-8
  Journal NLM ID: 0151434
  Publisher: Elsevier
  Correspondence: yoshida@pheasant.pharm.okayama-u.ac.jp
  Institutions: Kyoto Pharmaceutical University, Kyoto, Japan, Faculty of Pharmaceutical Sciences, Okayama University, Okayama, Japan
  Methods: 13C NMR, 1H NMR, NMR-2D, ESI-MS, HPLC, UV, enzymatic digestion, extraction, optical rotation measurement, CC, RP-HPLC, HR-ESI-MS
  
   
  
  Coleogyne ramosissima
  CSDB ID 66352 (all data & tools)