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1. (Article ID: 11507)
Wu T, Leu Y, Chan Y
Aristofolin-A, a denitro-aristolochic acid glycoside and other constituents from Aristolochia kaempferi
Phytochemistry 49(8) (1998)
2509-2510
A denitro-aristolochic acid derivative, aristofolin-A, together with ten known compounds, were isolated from the fresh flowers of Aristolochia kaempferi. The structures of these compounds were determined by spectral analysis.
amino acid, flavonoid, flowers, A. liukiunesis, Aristolochia kaempferi, Aristolochiaceae, denitro aristolochic acid
Publication DOI: 10.1016/S0031-9422(98)00223-4Journal NLM ID: 0151434Publisher: Elsevier
Institutions: Department of Chemistry, National Cheng Kung University, Tainan, Taiwan
Methods: 1H NMR, NOE, IR, UV, extraction, CC, NOESY, HR-FAB
The publication contains the following compound(s):
- Compound ID: 20490
|
b-D-Glcp-(1-3)-Subst
Subst = β-sitosterol = SMILES O{3}[C@H](C1)CC[C@@]2(C)C1=CC[C@]3([H])[C@@]2([H])CC[C@@]4(C)[C@]3([H])CC[C@]4([C@@H](C)CC[C@@H](CC)C(C)C)[H] |
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Structure type: monomer
Trivial name: daucosterol, β-daucosterol, β-sitosterol, β-sitosterol-β-D-glucoside, androsine, saxifragifolin B, β-sitosterol 3-O-β-D-glucopyranoside
Compound class: saponin glycoside, glycoside, steroid glycoside, triterpenoid glycoside
Reference(s) to other database(s): GenDB:MK026953.1
- Compound ID: 29475
|
b-D-Glcp-(1-6)-Subst-(8-1)-Me
Subst = 6,8-dihydroxy-aristolic acid II = SMILES O={11}C(O)c2cc1OCOc1c4c2ccc3{8}c(O)c{6}c(O)cc34 |
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Structure type: monomer
; 473.1082 [M-H]-
C23H21O11
Trivial name: aristofolin-A
Compound class: glycoside
- Compound ID: 29476
|
/Variants 0/-+
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a-L-Rhap-(1-6)-b-D-Glcp
/Variants 0/ is:
Quercetin-(3-1)-
OR (exclusively)
Kaempferol-(3-1)- |
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Structure type: oligomer
Trivial name: kaempferol-3-O-rutinoside, quercetin-3-O-rutinoside
Compound class: glycoside
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