다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기
Chemical & pharmaceutical bulletin, v.53 no.11, 2005년, pp.1416 - 1422
Xie, Haihui (Kyoto Pharmaceutical University) , Wang, Tao (Kyoto Pharmaceutical University) , Matsuda, Hisashi (Kyoto Pharmaceutical University) , Morikawa, Toshio (Kyoto Pharmaceutical University) , Yoshikawa, Masayuki (Kyoto Pharmaceutical University) , Tani, Tadato (Department of Kampo-pharmaceutics, Institute of Natural Medicine, Toyama Medical and Pharmaceutical University)
AI-Helper
The 80% aqueous acetone extract from the whole plant of Saussurea medusa MAXIM. was found to inhibit rat lens aldose reductase (IC50=1.4 μg/ml). From this extract, flavonoids, lignans, and quinic acid derivatives were isolated together with two new ionone glycosides, saussureosides A and B. Their...
Morikawa, Toshio, Sun, Bohang, Matsuda, Hisashi, Wu, Li Jun, Harima, Shoichi, Yoshikawa, Masayuki. Bioactive Constituents from Chinese Natural Medicines. XIV.New Glycosides of β-Carboline-Type Alkaloid, Neolignan, and Phenylpropanoid from Stellaria dichotoma L. var. lanceolata and Their Antiallergic Activities. Chemical & pharmaceutical bulletin, vol.52, no.10, 1194-1199.
1749-8546 Dictionary of Traditional Chinese Medicines Shanghai Scientific and Technologic 1482 1985
1340-3443 Nat. Med. YANG R-P 51 2 134 1997 10.1038/38154
0022-2062 J. Jpn. Bot. YANG R-P 78 6 315 2003
Takasaki, Midori, Konoshima, Takao, Komatsu, Katsuko, Tokuda, Harukuni, Nishino, Hoyoku. Anti-tumor-promoting activity of lignans from the aerial part of Saussurea medusa. Cancer letters, vol.158, no.1, 53-59.
Duan, Hongquan, Takaishi, Yoshihisa, Momota, Hiroshi, Ohmoto, Yasukazu, Taki, Takao. Immunosuppressive constituents from Saussurea medusa. Phytochemistry, vol.59, no.1, 85-90.
0968-0896 Bioorg. Med. Chem. Fan C. Q., Yue J. M. 11 703 2003 10.1016/S0968-0896(02)00470-4
Lanzhou Daxue Xuebao, Ziran Kexueban Jia Z., Fei H., Li Y., Zhu Z. 20 126 20
0251-0790 Gaodeng Xuexiao Huaxue Xuebao Jia Z., Fei H., Li Y., Zhu Z. 7 789 1986
0251-0790 Gaodeng Xuexiao Huaxue Xuebao Jia Z., Gong N., Du M. 11 202 1986
0163-3864 J. Nat. Prod. SUN B 67 9 1464 2004 10.1021/np040080a
0032-0943 Planta Med. Matsuda H., Morikawa T., Xie H., Yo 70 847 2004 10.1055/s-2004-827234
Tao, Jing, Morikawa, Toshio, Ando, Shin, Matsuda, Hisashi, Yoshikawa, Masayuki. Bioactive Constituents from Chinese Natural Medicines. XI.Inhibitors on NO Production and Degranulation in RBL-2H3 from Rubia yunnanensis: Structures of Rubianosides II, III, and IV, Rubianol-g, and Rubianthraquinone. Chemical & pharmaceutical bulletin, vol.51, no.6, 654-662.
Morikawa, T., Tao, J., Ando, S., Matsuda, H., Yoshikawa, M.. Absolute Stereostructures of New Arborinane-Type Triterpenoids and Inhibitors of Nitric Oxide Production from Rubia yunnanensis1. Journal of natural products, vol.66, no.5, 638-645.
Tao, Jing, Morikawa, Toshio, Toguchida, Iwao, Ando, Shin, Matsuda, Hisashi, Yoshikawa, Masayuki. Inhibitors of nitric oxide production from the bark of Myrica rubra: structures of new biphenyl type diarylheptanoid glycosides and taraxerane type triterpene. Bioorganic & medicinal chemistry, vol.10, no.12, 4005-4012.
Morikawa, T., Matsuda, H., Toguchida, I., Ueda, K., Yoshikawa, M.. Absolute Stereostructures of Three New Sesquiterpenes from the Fruit ofAlpinia oxyphylla with Inhibitory Effects on Nitric Oxide Production and Degranulation in RBL-2H3 Cells1. Journal of natural products, vol.65, no.10, 1468-1474.
Matsuda, Hisashi, Morikawa, Toshio, Tao, Jing, Ueda, Kazuho, Yoshikawa, Masayuki. Bioactive Constituents of Chinese Natural Medicines. VII. Inhibitors of Degranulation in RBL-2H3 Cells and Absolute Stereostructures of Three New Diarylheptanoid Glycosides from the Bark of Myrica rubra. Chemical & pharmaceutical bulletin, vol.50, no.2, 208-215.
0009-2363 Chem. Pharm. Bull. KUBO M 34 8 3097 1986 10.1248/cpb.34.3097
Nawwar, M.A.M., Hussein, S.A.M., Merfort, I.. Leaf phenolics of Punica granatum. Phytochemistry, vol.37, no.4, 1175-1177.
Wang, M., Simon, J. E., Aviles, I. F., He, K., Zheng, Q.-Y., Tadmor, Y.. Analysis of Antioxidative Phenolic Compounds in Artichoke (Cynara scolymus L.). Journal of agricultural and food chemistry, vol.51, no.3, 601-608.
Hong-Yu, L., Koike, K., Ohmoto, T.. Triterpenoid saponins from Dianthus chinensis. Phytochemistry, vol.35, no.3, 751-756.
0163-3864 J. Nat. Prod. Tomas F., Ferreres F., Barberan F. 48 506 1985 10.1021/np50039a038
Markham, K.R., Ternai, B., Stanley, R., Geiger, H., Mabry, T.J.. Carbon-13 NMR studies of flavonoids-III - Naturally occurring flavonoid glycosides and their acylated derivatives. Tetrahedron, vol.34, no.9, 1389-1397.
0009-2363 Chem. Pharm. Bull. Fukunaga T., Kajikawa I., Nishiya K 36 1185 1986 10.1248/cpb.36.1185
Chiba, M., Hisada, S., Nishibe, S., Thieme, H.. 13CNMR analysis of symplocosin and (+)-epipinoresinol glucoside. Phytochemistry, vol.19, no.2, 335-336.
0009-2363 Chem. Pharm. Bull. KOBAYASHI H 33 4 1452 1985 10.1248/cpb.33.1452
Rahman, M.M.A., Dewick, P.M., Jackson, D.E., Lucas, J.A.. Lignans of Forsythia intermedia. Phytochemistry, vol.29, no.6, 1971-1980.
10.1002/(SICI)1096-9888(199606)31:6<602::AID-JMS338>3.0.CO;2-9
Flamini, Guido, Antognoli, Elena, Morelli, Ivano. Two flavonoids and other compounds from the aerial parts of Centaurea bracteata from Italy. Phytochemistry, vol.57, no.4, 559-564.
0031-9422 Phytochemistry Rumbero-Sanchez A., Vazquez P. 30 311 1991 10.1016/0031-9422(91)84144-H
Greca, Marina Della, Ferrara, Maria, Fiorentino, Antonio, Monaco, Pietro, Previtera, Lucio. Antialgal compounds from zantedeschia aethiopica. Phytochemistry, vol.49, no.5, 1299-1304.
Comte, Gilles, Allais, Daovy P., Chulia, Albert J., Vercauteren, Joseph, Pinaud, Noel. Three phenylpropanoids from Juniperus phœnicea. Phytochemistry, vol.44, no.6, 1169-1173.
0009-2363 Chem. Pharm. Bull. MIYASE T 36 7 2475 1988 10.1248/cpb.36.2475
0009-2363 Chem. Pharm. Bull. MIYASE T 35 3 1109 1987 10.1248/cpb.35.1109
0009-2363 Chem. Pharm. Bull. KITAJIMA J 46 10 1587 1998 10.1248/cpb.46.1587
0009-2363 Chem. Pharm. Bull. MIZUTANI K 36 7 2689 1988 10.1248/cpb.36.2689
37) Those known constituents were identified by comparison of their physical data with commercially obtained samples.
Voutquenne, Laurence, Lavaud, Catherine, Massiot, Georges, Sevenet, Thierry, Hadi, Hamid A.. Cytotoxic polyisoprenes and glycosides of long-chain fatty alcohols from Dimocarpus fumatus. Phytochemistry, vol.50, no.1, 63-69.
0009-2363 Chem. Pharm. Bull. DEYAMA T 35 5 1785 1987 10.1248/cpb.35.1785
10.1016/0031-9422(82)85054-1
Fonseca, S.F., de Paiva Campello, J., Barata, L.E.S., Ruveda, E.A.. 13C NMR spectral analysis of lignans from Araucaria angustifolia. Phytochemistry, vol.17, no.3, 499-502.
0009-2363 Chem. Pharm. Bull. 29 8 2391 1981 10.1248/cpb.29.2391
0022-3263 J. Org. Chem. 57 20 5370 1992 10.1021/jo00046a018
0009-2363 Chem. Pharm. Bull. KITAJIMA J 42 3 608 1994 10.1248/cpb.42.608
Furukawa, Satomi, Takagi, Naomichi, Ikeda, Tsuyoshi, Ono, Masateru, Nafady, Alaa Mohamed, Nohara, Toshihiro, Sugimoto, Hiroyuki, Doi, Shima, Yamada, Hideo. Two Novel Long-Chain Alkanoic Acid Esters of Lupeol from Alecrim-Propolis. Chemical & pharmaceutical bulletin, vol.50, no.3, 439-440.
Magn. Res. Chem. Reynolds W. F., McLean S., Tay L. L 35 455 1997 10.1002/(SICI)1097-458X(199707)35:7<455::AID-OMR116>3.0.CO;2-6
47) The 1 H- and 13 C-NMR spectra of 1 , 2 , 1a , and 2a were assigned with the aid of distortionless enhancement by polarization transfer (DEPT), homo- and hetero-correlation spectroscopy ( 1 H- 1 H, 13 C- 1 H COSY), and HMBC experiments.
Yokosuka, A., Mimaki, Y., Sashida, Y.. Steroidal Saponins from Dracaena surculosa. Journal of natural products, vol.63, no.9, 1239-1243.
Ohtani, Ikuko, Kusumi, Takenori, Kashman, Yoel, Kakisawa, Hiroshi. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids. Journal of the American Chemical Society, vol.113, no.11, 4092-4096.
50) Although the structure investigation of 2 was reported, 51) the absolute stereostructure was not determined. This is the first report of the structure elucidation including the absolute stereochemistry of 2 .
Shimizu, S., Miyase, T., Ueno, A., Usmanghani, K.. Sesquiterpene lactone glycosides and ionone derivative glycosides from Sonchus asper. Phytochemistry, vol.28, no.12, 3399-3402.
Matsuda, Hisashi, Morikawa, Toshio, Toguchida, Iwao, Yoshikawa, Masayuki. Structural Requirements of Flavonoids and Related Compounds for Aldose Reductase Inhibitory Activity. Chemical & pharmaceutical bulletin, vol.50, no.6, 788-795.
0009-2363 Chem. Pharm. Bull. YOSHIKAWA M 47 3 340 1999 10.1248/cpb.47.340
Matsuda, Hisashi, Morikawa, Toshio, Toguchida, Iwao, Harima, Shoichi, Yoshikawa, Masayuki. Medicinal Flowers. VI. Absolute Stereostructures of Two New Flavanone Glycosides and a Phenylbutanoid Glycoside from the Flowers of Chrysanthemum indicum L.: Their Inhibitory Activities for Rat Lens Aldose Reductase. Chemical & pharmaceutical bulletin, vol.50, no.7, 972-975.
0385-5414 Heterocycles MATSUDA H 55 8 1499 2001 10.3987/COM-01-9259
Yoshikawa, M., Murakami, T., Ishiwada, T., Morikawa, T., Kagawa, M., Higashi, Y., Matsuda, H.. New Flavonol Oligoglycosides and Polyacylated Sucroses with Inhibitory Effects on Aldose Reductase and Platelet Aggregation from the Flowers ofPrunus mume1. Journal of natural products, vol.65, no.8, 1151-1155.
0163-3864 J. Nat. Prod. MORIKAWA T 66 9 1191 2003 10.1021/np0301543
해당 논문의 주제분야에서 활용도가 높은 상위 5개 콘텐츠를 보여줍니다.
더보기 버튼을 클릭하시면 더 많은 관련자료를 살펴볼 수 있습니다.
*원문 PDF 파일 및 링크정보가 존재하지 않을 경우 KISTI DDS 시스템에서 제공하는 원문복사서비스를 사용할 수 있습니다.
출판사/학술단체 등이 한시적으로 특별한 프로모션 또는 일정기간 경과 후 접근을 허용하여, 출판사/학술단체 등의 사이트에서 이용 가능한 논문
Copyright KISTI. All Rights Reserved.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.