1989
DOI: 10.1016/0031-9422(89)80134-7
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Hydroxycinnamic acid esters of phenethylalcohol glycosides from Rehmannia glutinosa var. Purpurea

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Cited by 107 publications
(58 citation statements)
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“…Proton signals at δ 2.79 ppm (2H, t, J = 6.2 Hz, H-7), 3.79 ppm (1H, m, H-8a) and δ 4.05 ppm (1H, m, H-8b) revealed that the second aromatic system is part of a phenylethanoid moiety. The sugar resonances were again similar to that of (2), allowing the identifi cation of (3) as leucosceptoside A (Miyase et al, 1982;Sasaki et al, 1989). In previous investigations, leucosceptoside A was isolated together with iso-acteoside and acteoside out of the under terrestrial parts of Leucosceptrum japonicum (Miq.)…”
Section: Resultssupporting
confidence: 55%
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“…Proton signals at δ 2.79 ppm (2H, t, J = 6.2 Hz, H-7), 3.79 ppm (1H, m, H-8a) and δ 4.05 ppm (1H, m, H-8b) revealed that the second aromatic system is part of a phenylethanoid moiety. The sugar resonances were again similar to that of (2), allowing the identifi cation of (3) as leucosceptoside A (Miyase et al, 1982;Sasaki et al, 1989). In previous investigations, leucosceptoside A was isolated together with iso-acteoside and acteoside out of the under terrestrial parts of Leucosceptrum japonicum (Miq.)…”
Section: Resultssupporting
confidence: 55%
“…This is refl ected in the positive FAB-MS showing pseudomolecular peaks [M+Na] + at m/z 675 (4), respectively [M+Na] + at m/z 661 (5). The 1 H NMR spectrum of martynoside (4) showed a signal for a methoxy group at δ 3.89 ppm (3H, s, OCH 3 -3''') in the acid moiety and furthermore a signal at δ 3.81 ppm (3H, s, OCH 3 -4) in the phenylethanoid portion (Sasaki et al 1978;Miyase et al 1982;Calis et al 1984;Teborg and Junior 1989) (Figure 2), whereas jionoside D possesses only one methoxy group at δ 3.81 ppm (3H, s, OCH 3 -4) (Sasaki et al 1989). Martynoside (4) was isolated from Miyase and co-workers in 1982 from Leucosceptrum japonicum (Miq.)…”
Section: Resultsmentioning
confidence: 99%
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“…Chemical components in RG include iridoids glycosides, ionone glycosides, and phenylpropanoid glycosides [11][12][13]. Sixteen compounds were identified according to the method described above; the results are shown in Supplementary Table S1 [13][14][15][16][17][18][19][20]. Peak intensities of these compounds between the raw and processed RGs were analyzed by t-test (Table 2).…”
Section: Chemical Fingerprint Analysis Of Raw and Processed Rgmentioning
confidence: 99%
“…숙지황의 약성 및 효능이 생지황 및 건지황과 차이가 나는 것은 그 제조과정에서 함유성분의 함량 및 성상이 변화되기 때문인 것으로 알려져 있다. 지황의 주성 분은 iridoid로서 rehmaglutin A, B, C 및 D, iridoid 배당체 로서 catalpol, dihydrocatalpol, aucubin, leonuride, melittoside, rehmannioside A, B, C 및 D 등, 당류로서 raffinose, mannotriose 등 그리고 lysine, histidine 등의 아미노산과 β-sitosterol과 stigmasterol 등이 알려져 있고, 성분 중 catalpol은 생지황 및 건지황의 품질관리를 위한 지표물질로 이용되어 왔 다 (Nishimura et al, 1990;Kim et al, 2000;Nishimura et al, 1989;Oshio & Inouye, 1981;Sasaki et al, 1989;Shoyama et al, 1986;Shoyama et al, 1987;Takagi et al, 1982). 또한 최근 Lee 등 (2011)은 국내산 지황으로부터 β-sitosterol을 비롯한 24종의 화합물을 분리한 바 있다.…”
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