Show legend Show as text

Structure type: oligomer
Trivial name: martynoside
Compound class: glycoside, phenylpropanoid glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_189517,IEDB_225177,IEDB_885823,IEDB_983931,SB_192

• Article ID: 11317
  Takasaki M, Yamauchi I, Haruna M, Konoshima T "New glycosides from Ajuga decumbens" - Journal of Natural Products 61(9) (1998) 1105-1109
  

  A new phenethyl alcohol glycoside, galactosylmartynoside (1), and a new abietatriene-type diterpene glycoside, ajugaside A (2), were isolated from the whole plants of Ajuga decumbens, together with known phenethyl alcohol glycosides (3 and 4) and iridoid glycosides (5-7). Chemical structures were elucidated on the basis of spectral data. Of these compounds, 8-acetylharpagide (6) exhibited the strongest inhibitory effect on Epstein-Barr virus activation induced by 12-O-tetradecanoylphorbol-13-acetate.

  diterpenes, phenylpropanoid glycosides, tumor-promoting activities

  NCBI PubMed ID: 9748375
  Publication DOI: 10.1021/np980148k
  Journal NLM ID: 7906882
  Publisher: American Society of Pharmacognosy
  Institutions: Faculty of Pharmacy, Meijo University, Nagoya, Japan, Kyoto Pharmaceutical University, Kyoto, Japan
  Methods: 13C NMR, 1H NMR, NOE, IR, acid hydrolysis, HPLC, UV, extraction, optical rotation measurement, CC, melting point determination, HMBC, antitumor activity assay, DEPT, COSY, HOHAHA, HSQC, HR-FAB-MS
  
   
  
  Ajuga decumbens
  CSDB ID 61769 (all data & tools)
• Article ID: 12079
  Wei X-M, Zhu Q-X, Chen J-C, Cheng D-L "Two new iridoid glucosides from Clerodenrum serratum" - Kao Teng Hsueh Hsiao Hua Heush Hsueh Pao = Chemical Journal of Chinese Universities [Chinese] 21(11) (2000) 1675-1678
  

  Four compounds were obtained from the leaves of Clerodendrum serratum. By means of spectroscopic techniques(such as IR, UV, MS, 1H NMR , 13C NMR and 2D-NMR) and chemical evidences, their structures were elucidated as 7-O-p-coumaroyloxyugandoside(1), 7-O-cinnamoyloxyugandoside(2), acteoside(3) and martynoside(4) respectively. Compounds 1 and 2 were new iridoid glucosides, compunds 3 and 4 were phenylpropanoid glycosides which were obtained for the first time from this plant.

  2D-NMR, phenylpropanoid glycoside, Verbenaceae, iridoid glucoside, Clerodendrum serratum, Clerodenrum

  Journal NLM ID: 101279494
  WWW link: http://www.cjcu.jlu.edu.cn/EN/Y2000/V21/I11/1675
  Publisher: Changchun, China
  Institutions: Department of Chemistry, National Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, China
  Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, IR, UV, CC, melting point determination
  
   
  
  Clerodenrum serratum
  CSDB ID 65117 (all data & tools)

Show legend Show as text

Structure type: oligomer
Trivial name: darendoside B
Compound class: glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_189517,IEDB_225177,IEDB_885823,IEDB_983931,SB_192

• Article ID: 11317
  Takasaki M, Yamauchi I, Haruna M, Konoshima T "New glycosides from Ajuga decumbens" - Journal of Natural Products 61(9) (1998) 1105-1109
  

  A new phenethyl alcohol glycoside, galactosylmartynoside (1), and a new abietatriene-type diterpene glycoside, ajugaside A (2), were isolated from the whole plants of Ajuga decumbens, together with known phenethyl alcohol glycosides (3 and 4) and iridoid glycosides (5-7). Chemical structures were elucidated on the basis of spectral data. Of these compounds, 8-acetylharpagide (6) exhibited the strongest inhibitory effect on Epstein-Barr virus activation induced by 12-O-tetradecanoylphorbol-13-acetate.

  diterpenes, phenylpropanoid glycosides, tumor-promoting activities

  NCBI PubMed ID: 9748375
  Publication DOI: 10.1021/np980148k
  Journal NLM ID: 7906882
  Publisher: American Society of Pharmacognosy
  Institutions: Faculty of Pharmacy, Meijo University, Nagoya, Japan, Kyoto Pharmaceutical University, Kyoto, Japan
  Methods: 13C NMR, 1H NMR, NOE, IR, acid hydrolysis, HPLC, UV, extraction, optical rotation measurement, CC, melting point determination, HMBC, antitumor activity assay, DEPT, COSY, HOHAHA, HSQC, HR-FAB-MS
  
   
  
  Ajuga decumbens
  CSDB ID 61164 (all data & tools)