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²éѯ½á¹û£º¹²²éµ½313¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 6-Methoxynaringenin ÏàËÆ¶È:87.5% Natural Product Sciences 2010 16 207-210 Phytochemical Constituents from Salvia plebeia Lee, Ghang Tai; Duan, Chao Hui; Lee, Jung-Noh; Lee, Kwang-Sik; Hong, Jin-Tae; Lee, Kun-Kook Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . dihydroroxylin A ÏàËÆ¶È:81.2% Chinese Joumal of Experimental Traditional Medical Fomulae 2011 17 78-81 Triterpenoids from Gardenia jasminoides FU Xiao-mei , WANG Zheng-tao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (¡À) 5,7,4'-trihydroxy-8-methoxyflavanone C8H6O5 ÏàËÆ¶È:80% Shoyakugaku Zasshi 1986 40 432-433 Studies on the Constituents of Scutellaria Species (VIII) : On the Flavonoid Constituents of "Ban Zhi Lian," the Whole Herb of Scutellaria rivularis WALL (2) TOMIMORI TSUYOSHI, MIYAICHI YUKINORI, IMOTO YOSHITAKA, KIZU HARUHISA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 5,7,4'-Trihydroxy-8-methoxyflavanone C16H14O6 ÏàËÆ¶È:75% Chemistry of Natural Compounds 2002 38 473-519 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 5,7,4'-Trihydroxy-6-methoxyflavanone C16H14O6 ÏàËÆ¶È:75% Chemistry of Natural Compounds 2002 38 473-519 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (2R:3R)-2,3-dihydro-5,7,4'-trihydroxy-6-methoxyflavonol C16H14O7 ÏàËÆ¶È:75% Phytochemistry 1990 29 2865-2869 Dihydroflavonol sweeteners and other constituents from Hymenoxys turneri Feng Gao,Huiping Wang,Tom J. Mabry,A.Douglas Kinghorn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . dihydrooroxylin A ÏàËÆ¶È:75% Journal of Shenyang Pharmaceutical University 2003 20 181-183 Isolation and identif ication of the chemical constituents of roots of Scutellaria amoena C. H. Wright XIAO Li-he, WANG Hong-yan, SONG Shao-jiang, ZHANG Guang-ping, SONG Hai-xiu, XU Sui-xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 5,7-dihydroxy-6-methoxy-2-(4'-hydroxyphenyl0-2,3-dihydroxy-4H-1-benzopyran-4-one ÏàËÆ¶È:75% Journal of the Indian Chemical Society 2002 79 169-175 Stibenoids and flavonoids from the orchids Coelogyne uniflora,Ione paleacea and Acrochoene punctata P.L.Majumder,S.Chakraborty and S.Sen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 5,4'-dihydroxy-6,7-dimethoxyflavanone C17H16O6 ÏàËÆ¶È:73.3% Journal of Natural Products 1992 Vol 55 357 Isolation of Potential Cancer Chemopreventive Agents from Eriodictyon californicum Yong-Long Liu, David K. Ho, John M. Cassady, Vanessa M. Cook, William M. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 2(S)-5,7-dihydroxy-6-methoxyflavanone ÏàËÆ¶È:73.3% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 136-139 Chemical Constituents from the Ethyl Acetate Extract Parts of Qinzhu Siwu Tang YUAN Hai-mei, PENG Teng, HUANG Dao-qiu, LI Xiao-nian, LI Bo-qun, LING Zhi-qun, YANG Jing, HE Gang-min, LI Yu-chuan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 5,7,2'-trihydroxy-8-methoxyflavanone ÏàËÆ¶È:68.7% Natural Product Sciences 2006 12 205-209 Revision of Structures of Flavanoids from Scutellaria indica and Their Protein Tyrosine Phosphatase 1B Inhibitory Activity Min, Byung-Sun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (2S)-4',5,6,7-tetra-hydroxyflavanone6-O-¦Â-D-glucopyranoside ÏàËÆ¶È:68.4% Natural Product Research and Development 2014 26 60-63,32 Studies on Chemical Constituents and DPPH Free Radical Scavenging Activityof Carthamus tinctorius L. OLALEYE Olajide, LI Shan-shan, LIU Hai-tao, CHAI Xin, WANG Yue-fei *, GAO Xiu-mei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 5,4'-dihydroxy-6-C-methyl-7-methoxy flavanone C17H16O5 ÏàËÆ¶È:66.6% Phytochemistry 2000 55 965-970 C-Methyl-flavonoids from the leaf waxes of some Myrtaceae Eckhard Wollenweber, Ru¨¹diger Wehde, Marion Dörr, Gu¨¹nter Lang, Jan F. Stevens Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . naringenin ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2008 39 21-23 °ëÖ¦Á«»¯Ñ§³É·ÖµÄÑо¿ ÖÙºÆ;ѦÏþϼ;Ò¦ÇìÇ¿ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 2(S)-5,7,4'-ÈýôÇ»ù-6-¼×Ñõ»ù¶þÇâ»ÆÍª ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2011 36 3270-3275 Study on chemical constituents of Scutelliaria regeliana WANG, Jinlan, ZHAO, Baoying, XU, Hongmei, ZHAO, Ming, TANG, Wanxia, ZHANG, Shujun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (2S)-onysilin ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2014 45 2303-2306 Chemical constituents from active fraction in pericarps of Juglans mandshurica ZHOU Yuan-yuan, LIU Zhao-xi, MENG Ying, JIANG Yan-qiu, YANG Bing-you Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 5a ÏàËÆ¶È:62.5% Biochemical Systematics and Ecology 2006 34 588-592 Norlignans and homoisoflavanones from two South African Drimiopsis species (Hyacinthaceae: Hyacinthoideae) Chantal Koorbanally, Dulcie A. Mulholland, Neil R. Crouch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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