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Found 2 structures. Displayed structures from 1 to 2
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1. Compound ID: 28600

Compound 28600

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Structure type: oligomer ; 659.3287
C₃₂H₅₀O₁₄
Trivial name: ajugaside A
Compound class: glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192

The structure is contained in the following publication(s):

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 61165 (all data & tools)

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2. Compound ID: 28601

Compound 28601

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Structure type: monomer ; 519.2570 [M+Na]+
C₂₆H₄₀O₉
Compound class: glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192

The structure is contained in the following publication(s):

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 61166 (all data & tools)

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