CSDB: Search results

Found 4 structures. Displayed structures from 1 to 4
Expand all compounds Show all as text (SweetDB notation)

1. Compound ID: 32600

Compound 32600

Show legend
Show as text

Structure type: oligomer
Trivial name: inermoside
Compound class: glycoside
Contained glycoepitopes: IEDB_136105,IEDB_141806,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_241101,IEDB_885823,IEDB_983931,SB_192

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

Article ID: 12583
Park S-Y, Chang S-Y, Yook C-S, Nohara T "New 3,4-seco-lupane-type triterpene glycosides from Acanthopanax senticosus forma inermis" - Journal of Natural Products 63(12) (2000) 1630-1633

Four new 3,4-seco-lupane-type triterpene glycosides (1−4) were isolated from the leaves of Acanthopanax senticosus forma inermis. The structures of 1−4 were established as 11α-hydroxy-3,4-seco-lup-4(23),20(30)-dien-3-oic acid methyl ester 28-oic acid 28-O-α-l-rhamnopyranosyl-(1→4)-β-d-glucopyranosyl-(1→6)-β-d-glucopyranoside, designated as inermoside (1); 1-deoxychiisanoside (2); 24-hydroxychiisanoside (3); and 11-deoxyisochiisanoside (4) by 1H− 1H COSY and 1H−13C COSY(HMBC, HMQC) methods and FABMS.
glycosides, Acanthopanax senticosus f. inermis, seco-lupane-type triterpenes
NCBI PubMed ID: 11141103
Publication DOI: 10.1021/np000277c
Journal NLM ID: 7906882
Publisher: American Society of Pharmacognosy
Correspondence: Park S-Y <996p9052@pharm.stud.kumamoto-u.ac.jp>
Institutions: Faculty of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan, College of Pharmacy, Kyung-Hee University, Seoul, South Korea, Korea Food and Drug Administration, Seoul, South Korea
Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, TLC, HPLC, extraction, evaporation, centrifugation, HR-EI-MS

Acanthopanax senticosus f. inermis
CSDB ID 67304 (all data & tools)

Expand this compound

2. Compound ID: 32601

Compound 32601

Show legend
Show as text

Structure type: oligomer
Trivial name: 1-deoxychiisanoside
Compound class: glycoside
Contained glycoepitopes: IEDB_136105,IEDB_141806,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_241101,IEDB_885823,IEDB_983931,SB_192

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

Article ID: 12583
Park S-Y, Chang S-Y, Yook C-S, Nohara T "New 3,4-seco-lupane-type triterpene glycosides from Acanthopanax senticosus forma inermis" - Journal of Natural Products 63(12) (2000) 1630-1633

Four new 3,4-seco-lupane-type triterpene glycosides (1−4) were isolated from the leaves of Acanthopanax senticosus forma inermis. The structures of 1−4 were established as 11α-hydroxy-3,4-seco-lup-4(23),20(30)-dien-3-oic acid methyl ester 28-oic acid 28-O-α-l-rhamnopyranosyl-(1→4)-β-d-glucopyranosyl-(1→6)-β-d-glucopyranoside, designated as inermoside (1); 1-deoxychiisanoside (2); 24-hydroxychiisanoside (3); and 11-deoxyisochiisanoside (4) by 1H− 1H COSY and 1H−13C COSY(HMBC, HMQC) methods and FABMS.
glycosides, Acanthopanax senticosus f. inermis, seco-lupane-type triterpenes
NCBI PubMed ID: 11141103
Publication DOI: 10.1021/np000277c
Journal NLM ID: 7906882
Publisher: American Society of Pharmacognosy
Correspondence: Park S-Y <996p9052@pharm.stud.kumamoto-u.ac.jp>
Institutions: Faculty of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan, College of Pharmacy, Kyung-Hee University, Seoul, South Korea, Korea Food and Drug Administration, Seoul, South Korea
Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, TLC, HPLC, extraction, evaporation, centrifugation, HR-EI-MS

Acanthopanax senticosus f. inermis
CSDB ID 67305 (all data & tools)

Expand this compound

3. Compound ID: 32602

Compound 32602

Show legend
Show as text

Structure type: oligomer
Trivial name: 24-hydroxychiisanogenin
Compound class: glycoside
Contained glycoepitopes: IEDB_136105,IEDB_141806,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_241101,IEDB_885823,IEDB_983931,SB_192

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

Article ID: 12583
Park S-Y, Chang S-Y, Yook C-S, Nohara T "New 3,4-seco-lupane-type triterpene glycosides from Acanthopanax senticosus forma inermis" - Journal of Natural Products 63(12) (2000) 1630-1633

Four new 3,4-seco-lupane-type triterpene glycosides (1−4) were isolated from the leaves of Acanthopanax senticosus forma inermis. The structures of 1−4 were established as 11α-hydroxy-3,4-seco-lup-4(23),20(30)-dien-3-oic acid methyl ester 28-oic acid 28-O-α-l-rhamnopyranosyl-(1→4)-β-d-glucopyranosyl-(1→6)-β-d-glucopyranoside, designated as inermoside (1); 1-deoxychiisanoside (2); 24-hydroxychiisanoside (3); and 11-deoxyisochiisanoside (4) by 1H− 1H COSY and 1H−13C COSY(HMBC, HMQC) methods and FABMS.
glycosides, Acanthopanax senticosus f. inermis, seco-lupane-type triterpenes
NCBI PubMed ID: 11141103
Publication DOI: 10.1021/np000277c
Journal NLM ID: 7906882
Publisher: American Society of Pharmacognosy
Correspondence: Park S-Y <996p9052@pharm.stud.kumamoto-u.ac.jp>
Institutions: Faculty of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan, College of Pharmacy, Kyung-Hee University, Seoul, South Korea, Korea Food and Drug Administration, Seoul, South Korea
Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, TLC, HPLC, extraction, evaporation, centrifugation, HR-EI-MS

Acanthopanax senticosus f. inermis
CSDB ID 67306 (all data & tools)

Expand this compound

4. Compound ID: 32603

Compound 32603

Show legend
Show as text

Structure type: oligomer
Trivial name: 11-deoxyisochiisanoside
Compound class: glycoside
Contained glycoepitopes: IEDB_136105,IEDB_141806,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_241101,IEDB_885823,IEDB_983931,SB_192

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

Article ID: 12583
Park S-Y, Chang S-Y, Yook C-S, Nohara T "New 3,4-seco-lupane-type triterpene glycosides from Acanthopanax senticosus forma inermis" - Journal of Natural Products 63(12) (2000) 1630-1633

Four new 3,4-seco-lupane-type triterpene glycosides (1−4) were isolated from the leaves of Acanthopanax senticosus forma inermis. The structures of 1−4 were established as 11α-hydroxy-3,4-seco-lup-4(23),20(30)-dien-3-oic acid methyl ester 28-oic acid 28-O-α-l-rhamnopyranosyl-(1→4)-β-d-glucopyranosyl-(1→6)-β-d-glucopyranoside, designated as inermoside (1); 1-deoxychiisanoside (2); 24-hydroxychiisanoside (3); and 11-deoxyisochiisanoside (4) by 1H− 1H COSY and 1H−13C COSY(HMBC, HMQC) methods and FABMS.
glycosides, Acanthopanax senticosus f. inermis, seco-lupane-type triterpenes
NCBI PubMed ID: 11141103
Publication DOI: 10.1021/np000277c
Journal NLM ID: 7906882
Publisher: American Society of Pharmacognosy
Correspondence: Park S-Y <996p9052@pharm.stud.kumamoto-u.ac.jp>
Institutions: Faculty of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan, College of Pharmacy, Kyung-Hee University, Seoul, South Korea, Korea Food and Drug Administration, Seoul, South Korea
Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, TLC, HPLC, extraction, evaporation, centrifugation, HR-EI-MS

Acanthopanax senticosus f. inermis
CSDB ID 67307 (all data & tools)

Expand this compound

Execution: <1 sec