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【期刊论文】Three New Cyclopentanoid Monoterpenes from Picrorhiza scropulariiflora
叶文才, Hao Wang, Wen Cai Ye. Ren Wang Jiang, jia-jun Wu, Thomas W. Mak, Shou xun Zhao, Xin Sheng Yao.
Plant Med 2004; 2004; 70: 382-384,-0001,():
-1年11月30日
Three new cycloDentanold monoterpenes namecl piscrocins A (1) B (2)antl (3) were lsolateclcom the roots of Pic~orhnd sctophulariiflora (scrophulariaceae). The structures ofthese new compounds were establishecl by 1D antl 2D NMR spectroscopic techniques (HHCOSY, HMQC, HMBC, antl NOESY) In combination with X ray clystallographic analysis
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【期刊论文】Antisweet Saponins from Gymnema sylvestre
叶文才, Wencai Ye, Xin Liu, Qingwen Zhang, Chun-Tao Che, *
J. Nat. Prod. 2001, 64, 232-235,-0001,():
-1年11月30日
Three new oleanane-type triterpene glycosides (1-3), along with the sodium salt of alternoside II (4), were isolated from an ethanol extract of the leaves of Gymnema sylvestre. The structures of these new saponins were identified as 21, -O-benzoylsitakisogenin 3-O-, -D-glucopyranosyl(1f3)-, -D-glucuronopyranoside (1), the potassium salt of longispinogenin 3-O-‚-D-glucopyranosyl(1f3)-,-D-glucuronopyranoside (2), and the potassium salt of 29-hydroxylongispinogenin 3-O-,-D-glucopyranosyl(1f3)-,-D glucuronopyranoside (3). The aglycon of 3, gymnemagenol (3a), was characterized as 3., 16‚, 28, 29-tetrahydroxyolean-12-ene. Structure elucidation was accomplished by interpretation of NMR (DQF-COSY, HMQC, and HMBC) results, FABMS, and hydrolysis. Saponin 1 and the sodium salt of alternoside II (4) exhibited antisweet activity.
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【期刊论文】New Lupane Glycosides from Pulsatilla chinensis
叶文才, Wencai ye, Qingwen Zhang, Wendy W. L.Hsiao, Shouun Zhao. Chun-Tao Che
Planta Med2002; 68: 183-186,-0001,():
-1年11月30日
A new lupane type triterpenic acid, pulsatillic acid, and two new lupane type triterpenoid glycosides, pulsati Uoside A and B, along with the known 23-hydroxybetulinic acid were isolated from the roots of Pulsatilla chinensis. Their structures were characterized as 3-oxo-23-hydroxy-lup-20(29)-en-28-oic acid, 3fl, 23-dihydroxy-lup-20(29)-en-28-oic acid 3-O-a-L-arabinopyranoside and 3/3, 23-dihydroxy-lup-20(29)-en-28-oic acid 28-0-/3-0- glucopyranosyl-(1-6)-/3-o-glucopyranoside on the basis of hydrolysis and spectral evidence including two-dimensional relay HOHAHA, one-dimensional multiple relay COSY and ROESY NMR techniques. Pulsatillic acid exhibited cytotoxic activities against P-388, Lewis lung carcinoma and human large-cell lung carcinoma.
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【期刊论文】TRITERPENOIDS FROM PULSATILLA CHINENSIS
叶文才, WEN-CAI YE*, NINE-NING JI, SHOU-XUN ZHAO, JING-HAN LIO, TAO YE, *†‡ M. A. MCKERVEY† and E STEVENSON†
Phytochemistry, Vol. 42, No.3, pp. 799-802, 1996,-0001,():
-1年11月30日
A new lupane type triterpenic acid, pulsatillic acid, and two new lupane type triterpenoid glycosides, pulsatiUoside A and B, along with the known 23-hydroxybetulinic acid were isolated from the roots of Pulsatilla chinensis. Their structures were characterized as 3-oxo-23-hydroxy-lup-20(29)-en-28-oic acid, 3fl, 23-dihydroxy-lup-20(29)-en-28-oic acid 3-O-a-L-arabinopyranoside and 3/3, 23-dihydroxy-lup-20(29)-en-28-oic acid 28-0-/3-0- glucopyranosyl-(1-6)-/3-o-glucopyranoside on the basis of hydrolysis and spectral evidence including two-dimensional relay HOHAHA, one-dimensional multiple relay COSY and ROESY NMR techniques. Pulsatillic acid exhibited cytotoxic activities against P-388, Lewis lung carcinoma and human large-cell lung carcinoma.
Pulsatilla chinensis, Ranunculaceae, triterpenic acid, triterpenoid glycosides, 23-hydroxybetulinic acid, pulsatillic acid, pulsatilloside A and B.,
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【期刊论文】Five New Triterpene Saponins from Pulsatilla patens var. multifida
叶文才, Wencai Ye, Guoshi Pan, Qingwen Zhang, Chun-Tao Che, *, Houming Wu
J. Nat. Prod. 1999, 62, 233-237,-0001,():
-1年11月30日
The roots of several Pulsatilla species (Ranunculaceae) are used for "blood-cooling" and detoxifying effects in traditional Chinese medicine.1 A number of Pulsatilla species, such as P. ambigua, P. chinensis, P. dahurica, P. koreana, and P. turczaninovii, are employed in treating diarrhea, vaginal trichromoniasis, and bacterial infections, and pharmacological investigations have suggested that the triterpene saponins are important bioactive components. 2-6 We have previously reported on the isolation and structural elucidation of new triterpene glycosides such as pulsatillosides A and B from P. chinensis 5 and patensin from P. patens var. multifida.6 Further investigation of the latter plant has now led to the purification of additional saponin constituents. In this paper we describe the isolation of seven saponins, the structures of which were determined with the aid of 1D and 2D NMR (13C, 1H, HMQC, HMBC, and ROESY) techniques, FABMS, and hydrolysis. An extensive search of the literature 7-11 indicated thatcompounds 1-5 are new structures.
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