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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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
2Â¥2014-12-13 12:40:58
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