| 3 | 1/1 | б |
| 鿴: 545 | ؏(f): 2 | ||
zky_panmengľx (ʽ)
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[]
Vƶȴ80%ʮָx 2˅c
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5# C5D5N 62.3,73.6,75.1,78.3,78.4,100.5,102.9,106.6,107.2,127.3,129.9,131.2,132.2,132.7,157.8,158.1,164.6,172.6,183.5 |
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. chrysin-7-glucoside C21H20O9 ƶ:73.6% World Science and Technology-Modernization of Traditional Chinese Medicine and Materia Medica 2007 9 64-67 Chemical Constituents of P.Canadensis Moench.Buds Wang Xiangxiang, Zhou Lidong, Nan Yao, Meng Qinwei Structure 13C NMR Structure & 13C NMR ̼VģMD -------------------------------------------------------------------------------- 2 . S ƶ:66.6% Chinese Traditional and Herbal Drugs 1998 29 443-444 fW(xu)ɷֵо() ,_,,ĺ,־ Structure 13C NMR Structure & 13C NMR ̼VģMD -------------------------------------------------------------------------------- 3 . baicalein 6-methylether-7-O--galactopyranuronoside ƶ:65% Phytochemistry 2002 61 433-437 Flavonoid glycosides from Centaurea pseudoscabiosa subsp.pseudoscabiosa from Turkey Guido Flamini, Maria Pardini, Ivano Morelli, Kuddisi Ertugrul,Huseyin Dural, Yavuz Bagci, Mustafa Kargioglu Structure 13C NMR Structure & 13C NMR ̼VģMD -------------------------------------------------------------------------------- 4 . protogenkwanin 4'-O--D-glucoside ƶ:63.6% Chemical & Pharmaceutical Bulletin 1987 35 4757-4762 Chemical and Chemotaxonomical Studies of Ferns. LXXIII. New Flavonoids with Modified B-Ring from the Genus Pseudophegopteris (Thelypteridaceae) HIROSHI WADA,HIROYUKI FUJITA,TAKAO MURAKAMI,YASUHISA SAIKI and CHIU-MING CHEN Structure 13C NMR Structure & 13C NMR ̼VģMD -------------------------------------------------------------------------------- 5 . Homoplantaginin ƶ:63.1% Archives of Pharmacal Research 2012 35 1347-1354 Antiviral activity of Aloe hijazensis against some haemagglutinating viruses infection and its phytoconstituents Howaida I. Abd-Alla, Nagat S. Abu-Gabal, Amal Z. Hassan, Mounir M. El-Safty and Nagwa M. M. Shalaby Structure 13C NMR Structure & 13C NMR ̼VģMD -------------------------------------------------------------------------------- 6 . ǧӼ A ƶ:63.1% Chinese Pharmaceutical Journal 2012 47 1366-1369 Liposoluble Constituents from Dichrocephala benthamii C.B.Clarke TIAN Xin-hui; DING Gang; PENG Chao-zhong; HU Yan-bao; MA Zhuo; ZOU Zhong-mei Structure 13C NMR Structure & 13C NMR ̼VģMD -------------------------------------------------------------------------------- 7 . 5,7-Dihydroxy-6-methoxyflavone |
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1 . chrysin-7-glucoside C21H20O9 ƶ:73.6% World Science and Technology-Modernization of Traditional Chinese Medicine and Materia Medica 2007 9 64-67 Chemical Constituents of P.Canadensis Moench.Buds Wang Xiangxiang, Zhou Lidong, Nan Yao, Meng Qinwei Structure 13C NMR ̼VģMD 2 . S ƶ:66.6% Chinese Traditional and Herbal Drugs 1998 29 443-444 fW(xu)ɷֵо() ,_,,ĺ,־ Structure 13C NMR ̼VģMD 3 . baicalein 6-methylether-7-O--galactopyranuronoside ƶ:65% Phytochemistry 2002 61 433-437 Flavonoid glycosides from Centaurea pseudoscabiosa subsp.pseudoscabiosa from Turkey Guido Flamini, Maria Pardini, Ivano Morelli, Kuddisi Ertugrul,Huseyin Dural, Yavuz Bagci, Mustafa Kargioglu Structure 13C NMR ̼VģMD 4 . protogenkwanin 4'-O--D-glucoside ƶ:63.6% Chemical & Pharmaceutical Bulletin 1987 35 4757-4762 Chemical and Chemotaxonomical Studies of Ferns. LXXIII. New Flavonoids with Modified B-Ring from the Genus Pseudophegopteris (Thelypteridaceae) HIROSHI WADA,HIROYUKI FUJITA,TAKAO MURAKAMI,YASUHISA SAIKI and CHIU-MING CHEN Structure 13C NMR ̼VģMD 5 . Homoplantaginin ƶ:63.1% Archives of Pharmacal Research 2012 35 1347-1354 Antiviral activity of Aloe hijazensis against some haemagglutinating viruses infection and its phytoconstituents Howaida I. Abd-Alla, Nagat S. Abu-Gabal, Amal Z. Hassan, Mounir M. El-Safty and Nagwa M. M. Shalaby Structure 13C NMR ̼VģMD 6 . ǧӼ A ƶ:63.1% Chinese Pharmaceutical Journal 2012 47 1366-1369 Liposoluble Constituents from Dichrocephala benthamii C.B.Clarke TIAN Xin-hui; DING Gang; PENG Chao-zhong; HU Yan-bao; MA Zhuo; ZOU Zhong-mei Structure 13C NMR ̼VģMD |
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[] {(dio) +5 | ֮Ϧ 2026-03-24 | 5/250 |
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[] 070300W(xu){(dio) +9 | Է 2026-03-20 | 9/450 |
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[] һ־Ը211 ԇ270 {(dio) +5 | ϰ 2026-03-23 | 6/300 |
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[] όI(y){(dio) +11 | hanamiko 2026-03-18 | 11/550 |
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[] 336{(dio) +4 | յVS 2026-03-20 | 4/200 |
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[] 328{(dio) +4 | LHHL66 2026-03-23 | 4/200 |
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[] 289c085600B^(q){(dio) +3 | @ôզ 2026-03-22 | 4/200 |
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[] 287{(dio) +8 | 辀cǺ 2026-03-19 | 9/450 |
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[] 275{(dio) +6 | shansx 2026-03-22 | 8/400 |
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[] {(dio) +5 | @taotao 2026-03-21 | 5/250 |
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[] όW(xu)W(xu)T080502 337{(dio)-һ־ԸAпƼW(xu) +4 | mr 2026-03-18 | 5/250 |
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[] һ־ԸAώ 070300W(xu)304{(dio) +3 | 0703ܷѩ304 2026-03-18 | 3/150 |
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[] 330{(dio) +4 | СĻ 2026-03-18 | 4/200 |
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[] 288{(dio) +16 | ں 2026-03-19 | 16/800 |
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[] {(dio)һ־ԸϾպW(xu)289 +3 | @taotao 2026-03-19 | 3/150 |
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[] 353{(dio) +3 | ^S׃ 2026-03-20 | 3/150 |
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[] {(dio) +3 | @taotao 2026-03-20 | 3/150 |
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[] 085410˹܌T317{(dio)0854ԣ +4 | xbxudjdn 2026-03-18 | 4/200 |
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112 2026-03-19 | 3/150 |
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[] һ־Ը288ЙC(j)W(xu){(dio) +3 | Сľx200408204 2026-03-18 | 3/150 |
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