中醫藥瀏覽 TCM Profile
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藥材   Compound  
金銀花 3,4-di-o-caffeoyl,quinic,acid
3,4-diferuoylquinic,acid
3,5-di-o-caffeoylquinic,acid
3-caffeoylquinic,acid
3-o-caffeoylquinic,acid
3-o-caffeoylquinic,acid,butyl,ester
3-o-[alpha-l-rhamnopyranosyl-(1-2)-,alpha-l-arabinopyranosyl],hederagenin
4,5-di-o-caffeoyl,quinic,acid
7-epi-loganin
7-epi-vogeloside
caffeic,acid,(ca)
centauroside
chlorogenetic,acid
Chlorogenic acid
chlorogenic,acid
dimethyl-secoxyloganoside
dipsacoside,b
hederagenin-28-o-[beta-d-glucopyranosyl-(1-6)-,beta-d-glucopyranosyl],ester
hyperoside
isoquercetin
loganin
lonicerin
luteolin-7-monoglucoside
luteolin-7-o-beta-d-galactopyranoside
luteolin-7-o-beta-d-glucoside
luteolin-7-O-beta-D-neohesperidoside
macranthoidin,a
macranthoidin,b
macranthoside,a
macranthoside,b
neo-chlorogenic,acid
quercertin,3-o-beta-d-glucopyranoside
quercetin
quercetin 3-O-rhamnopyranosyl
quercetin,3-o-glucoside
quercetin,3-o-rutinoside
quercetin-3-o-galactopyranoside
secoxyloganin
tricin-7-o-beta-d-glucoside
TOP
參考文獻
[1] Li, H. J., Li, P., Ye, W. C., Determination of five major iridoid glucosides in Flos Lonicerae by high-performance liquid chromatography coupled with evaporative light scattering detection. J Chromatogr A 2003, 1008, 167-172
[2] Ren, M. T., Chen, J., Song, Y., Sheng, L. S., et al., Identification and quantification of 32 bioactive compounds in Lonicera species by high performance liquid chromatography coupled with time-of-flight mass spectrometry. J Pharm Biomed Anal 2008, 48, 1351-1360.
金銀花 3,4-di-o-caffeoylquinic,acid
3,5-di-o-caffeoylquinic,acid
3-caffeoylquinic,acid
3-o-caffeoylquinic,acid
3-o-caffeoylquinic,acid,butyl,ester
3-o-[alpha-l-rhamnopyranosyl-(1-2)-,alpha-l-arabinopyranosyl],hederagenin
7-epi-loganin
7-epi-vogeloside
caffeic,acid,(ca)
centauroside
chlorogenetic,acid
Chlorogenic acid
chlorogenic,acid
dimethyl-secoxyloganoside
dipsacoside,b
hederagenin-28-o-[beta-d-glucopyranosyl-(1-6)-,beta-d-glucopyranosyl],ester
hyperoside
isoquercetin
loganin
lonicerin
luteolin-7-monoglucoside
luteolin-7-o-beta-d-galactopyranoside
luteolin-7-o-beta-d-glucoside
luteolin-7-O-beta-D-neohesperidoside
macranthoidin,a
macranthoidin,b
macranthoside,a
macranthoside,b
neo-chlorogenic,acid
pheophytin,a
quercertin,3-o-beta-d-glucopyranoside
quercetin
quercetin 3-O-rhamnopyranosyl
quercetin,3-o-glucoside
quercetin,3-o-rutinoside
quercetin-3-o-galactopyranoside
secoxyloganin
tricin-7-o-beta-d-glucoside
TOP
參考文獻
[1] Wang, S. Y., Tseng, C. P., Tsai, K. C., Lin, C. F., et al., Bioactivity-guided screening identifies pheophytin a as a potent anti-hepatitis C virus compound from Lonicera hypoglauca Miq. Biochem Biophys Res Commun 2009, 385, 230-235.
[2] Li, H. J., Li, P., Ye, W. C., Determination of five major iridoid glucosides in Flos Lonicerae by high-performance liquid chromatography coupled with evaporative light scattering detection. J Chromatogr A 2003, 1008, 167-172.
[3] Ren, M. T., Chen, J., Song, Y., Sheng, L. S., et al., Identification and quantification of 32 bioactive compounds in Lonicera species by high performance liquid chromatography coupled with time-of-flight mass spectrometry. J Pharm Biomed Anal 2008, 48, 1351-1360.
金銀花 3,4-di-o-caffeoyl,quinic,acid
3,4-diferuoylquinic,acid
3,5-di-o-caffeoyl,quinic,acid
3-caffeoylquinic,acid
3-o-caffeoylquinic,acid
3-o-[alpha-l-rhamnopyranosyl-(1-2)-,alpha-l-arabinopyranosyl],hederagenin
4,5-di-o-caffeoyl,quinic,acid
7-epi-loganin
7-epi-vogeloside
caffeic,acid,(ca)
centauroside
chlorogenetic,acid
Chlorogenic acid
chlorogenic,acid
dimethyl-secoxyloganoside
dipsacoside,b
hederagenin-28-o-[beta-d-glucopyranosyl-(1-6)-,beta-d-glucopyranosyl],ester
hyperoside
isochlorogenic,acid
isoquercetin
loganin
lonicerin
luteolin-7-monoglucoside
luteolin-7-o-beta-d-galactopyranoside
luteolin-7-o-beta-d-glucoside
luteolin-7-O-beta-D-neohesperidoside
macranthoidin,a
macranthoidin,b
macranthoside,a
macranthoside,b
neo-chlorogenic,acid
quercertin,3-o-beta-d-glucopyranoside
quercetin
quercetin 3-O-rhamnopyranosyl
quercetin,3-o-glucoside
quercetin,3-o-rutinoside
quercetin-3-o-galactopyranoside
secoxyloganin
tricin-7-o-beta-d-glucoside
TOP
參考文獻
[1] Li, H. J., Li, P., Ye, W. C., Determination of five major iridoid glucosides in Flos Lonicerae by high-performance liquid chromatography coupled with evaporative light scattering detection. J Chromatogr A 2003, 1008, 167-172.
[2] Ren, M. T., Chen, J., Song, Y., Sheng, L. S., et al., Identification and quantification of 32 bioactive compounds in Lonicera species by high performance liquid chromatography coupled with time-of-flight mass spectrometry. J Pharm Biomed Anal 2008, 48, 1351-1360.
金銀花 (e)-aldosecologanin
(e,z)-2,4-decadienal
(r)-3,7-dimethyl-6-octen-1-ol
(z)-3-hexen-1-ol
(z)-3-hexenyl,tiglate
(z)-aldosecologanin
1,3-o-dicaffeoyl,quinic,acid
1,4-o-dicaffeoyl,quinic,acid
1,5-o-dicaffeoyl,quinic,acid
1-o-caffeoylquinic,acid
2-hydroxy-benzoic,acid,,methyl,ester
2-Methyl-1-butanol
3'-Methoxy-4',5,7-trihydroxyflavone
3,4-di-o-caffeoyl,quinic,acid
3,4-diferuoylquinic,acid
3,4-o-dicaffeoyl,quinic,acid
3,5-di-o-caffeoyl,quinic,acid
3,5-dicaffeoylquinic,acid,buthyl,ester
3,5-dicaffeoylquinic,acid,methyl,ester
3,5-o-dicaffeoyl,quinic,acid
3-caffeoylquinic,acid
3-hexen-1-ol
3-O-beta-D-Glucopyranosyl-(1-3)-alpha-L-rhamnopyranosyl-(1-2)-alpha-L-arabino-pyranosyl-hederagenin-28-O-beta-D-glucopyranosyl-(1-6)-beta-D-glucopyranosyl ester
3-o-caffeoylquinic,acid
3-o-caffeoylquinic,acid,butyl,ester
3-o-[alpha-l-rhamnopyranosyl-(1-2)-,alpha-l-arabinopyranosyl],hederagenin
4,5-di-o-caffeoyl,quinic,acid
4,5-o-dicaffeoyl,quinic,acid
4-o-caffeoylquinic,acid
5-o-caffeoyl,quinic,acid
7-epi-loganin
7-epi-vogeloside
7-o-(4-beta-d-glucopyranosyloxy-3-methoxybenzoyl),secologanolic,acid
7-o-butylsecologanic,acid
8-epi-loganin
8-epi-loganin,acid
alpha-Teripineol
apigenin
B-Germacrene
Benzyl alcohol
Benzyl benzoate
Benzyl ethyl alcohol
beta-bourbonene
beta-caryophyllene
beta-Sitosterol
beta-Sitosterol-beta-D-glucoside
caffeic,acid,(ca)
caryophyllene
centauroside
chlorogenetic,acid
Chlorogenic acid
chlorogenic,acid
chrysin
chrysoeirol-7-o-neohesperidoside
cis-jasmone
citronellol
dimethyl-secologanoside
dimethyl-secoxyloganoside
dipsacoside,b
epi-vogeloside
Ethylpalmitate
Eugenol
geranylacetone
germacrene,d
hederagenin-28-o-[beta-d-glucopyranosyl-(1-6)-,beta-d-glucopyranosyl],ester
hexenyl,benzoate
hyperoside
indole
isocaryophyllene
isochlorogenic,acid
isoquercetin
l-phenylalaninosecologanin
linalool
linalool,oxide
Loganic acid
loganin
loganin,acid
loniceracetalide,a
lonicerin
loniceroside,c
loniflavone
lonijaposides,a
lonijaposides,a1
lonijaposides,a2
lonijaposides,a3
lonijaposides,a4
lonijaposides,b
lonijaposides,b1
lonijaposides,b2
lonijaposides,c
Luteolin
luteolin-7-monoglucoside
luteolin-7-o-beta-d-galactopyranoside
luteolin-7-o-beta-d-glucoside
luteolin-7-O-beta-D-neohesperidoside
luteolin-7-o-galactoside
macranthoidin,a
macranthoidin,b
macranthoside,a
macranthoside,b
methyl,3,4-di-o-caffeoyl,quinic,acid
methyl,3,5-di-o-caffeoyl,quinic,acid
methyl,benzoate
methyl,jasmonate
neo-chlorogenic,acid
nerolidol
ochnaflavone
phenylacetaldehyde
quercertin,3-o-beta-d-glucopyranoside
quercetin
quercetin 3-O-rhamnopyranosyl
quercetin,3-o-glucoside
quercetin,3-o-rutinoside
quercetin-3-o-galactopyranoside
secologanic,acid
secologanin
secologanin,dibutylacetal
secologanin,dimethylacetal
secologaniside-7-methyl,ester
secoxyloganin
secoxyloganin,7-butyl,ester
Stigmasterol
tricin-7-o-beta-d-glucoside
tricin-7-o-neohesperidoside
vogeloside
TOP
參考文獻
[1] Chang, C. W., Lin, M. T., Lee, S. S., Liu, K. C., et al., Differential inhibition of reverse transcriptase and cellular DNA polymerase-alpha activities by lignans isolated from Chinese herbs, Phyllanthus myrtifolius Moon, and tannins from Lonicera japonica Thunb and Castanopsis hystrix. Antiviral Res 1995, 27, 367-374.
[2] Lee, S. J., Shin, E. J., Son, K. H., Chang, H. W., et al., Anti-inflammatory Activity of the Major Constituents of Lonicera japonica. Arch. Pharm. Res 1995, 18, 133-135.
[3] Suh, S. J., Chung, T. W., Son, M. J., Kim, S. H., et al., The naturally occurring biflavonoid, ochnaflavone, inhibits LPS-induced iNOS expression, which is mediated by ERK1/2 via NF-kappaB regulation, in RAW264.7 cells. Arch Biochem Biophys 2006, 447, 136-146.
[4] Qian, Z. M., Wen, X. D., Li, H. J., Liu, Y., et al., Analysis of interaction property of bioactive components in Flos Lonicerae Japonicae with protein by microdialysis coupled with HPLC-DAD-MS. Biol Pharm Bull 2008, 31, 126-130.
[5] Qian, Z. M., Li, H. J., Li, P., Chen, J., Tang, D., Simultaneous quantification of seven bioactive components in Caulis Lonicerae Japonicae by high performance liquid chromatography. Biomed Chromatogr 2007, 21, 649-654.
[6] Qian, Z. M., Qin, S. J., Yi, L., Li, H. J., et al., Binding study of Flos Lonicerae Japonicae with bovine serum albumin using centrifugal ultrafiltration and liquid chromatography. Biomed Chromatogr 2008, 22, 202-206.
[7] Machida, K., Sasaki, H., Iijima, T., Kikuchi, M., Studies on the constituents of Lonicera species. XVII. New iridoid glycosides of the stems and leaves of Lonicera japonica THUNB. Chem Pharm Bull (Tokyo) 2002, 50, 1041-1044.
[8] Kwak, W. J., Han, C. K., Chang, H. W., Kim, H. P., et al., Loniceroside C, an antiinflammatory saponin from Lonicera japonica. Chem Pharm Bull (Tokyo) 2003, 51, 333-335.
[9] Peng, Y. Y., Liu, F. H., Ye, J. N., Determination of phenolic acids and flavones in Lonicera japonica Thumb. by capillary electrophoresis with electrochemical detection. Electroanalysis 2005, 17, 356-362.
[10] Peng, L. Y., Mei, S. X., Jiang, B., Zhou, H., Sun, H. D., Constituents from Lonicera japonica. Fitoterapia 2000, 71, 713-715.
[11] Schlotzhauer, W. S., Pair, S. D., Horvat, R. J., Volatile Constituents from the Flowers of Japanese Honeysuckle (Lonicera japonica). J. Agric. Food Chem. 1996, 44, 206-209.
[12] Song, W., Li, S., Wang, S., Wu, Y., et al., Pyridinium alkaloid-coupled secoiridoids from the flower buds of Lonicera japonica. J Nat Prod 2008, 71, 922-925.
[13] Chen, J., Li, S. L., Li, P., Song, Y., et al., Qualitative and quantitative analysis of active flavonoids in Flos Lonicerae by capillary zone electrophoresis coupled with solid-phase extraction. J Sep Sci 2005, 28, 365-372.
[14] Bhandari, P., Kumar, N., Gupta, A. P., Singh, B., Kaul, V. K., A rapid RP-HPTLC densitometry method for simultaneous determination of major flavonoids in important medicinal plants. J Sep Sci 2007, 30, 2092-2096.
[15] Tang, D., Li, H. J., Chen, J., Guo, C. W., Li, P., Rapid and simple method for screening of natural antioxidants from Chinese herb Flos Lonicerae Japonicae by DPPH-HPLC-DAD-TOF/MS. J Sep Sci 2008, 31, 3519-3526.
[16] Li, H. J., Li, P., Ye, W. C., Determination of five major iridoid glucosides in Flos Lonicerae by high-performance liquid chromatography coupled with evaporative light scattering detection. J Chromatogr A 2003, 1008, 167-172.
[17] TOMASSINI, L., COMETAM, M. F., SERAFINI, M., NICOLETTI, M., ISOLATION OF SECOIRIDOID ARTIFACTS FROM LONICERA JA PONICA. Journal of Natural Products 1995, 58, 1756-1758.
[18] Ren, M. T., Chen, J., Song, Y., Sheng, L. S., et al., Identification and quantification of 32 bioactive compounds in Lonicera species by high performance liquid chromatography coupled with time-of-flight mass spectrometry. J Pharm Biomed Anal 2008, 48, 1351-1360.
[19] Kakuda, R., Imai, M., Yaoita, Y., Machida, K., Kikuchi, M., Secoiridoid glycosides from the flower buds of Lonicera japonica. Phytochemistry 2000, 55, 879-881.
[20] Kumar, N., Singh, B., Bhandari, P., Gupta, A. P., et al., Biflavonoids from Lonicera japonica. Phytochemistry 2005, 66, 2740-2744.
[21] Qi, L. W., Chen, C. Y., Li, P., Structural characterization and identification of iridoid glycosides, saponins, phenolic acids and flavonoids in Flos Lonicerae Japonicae by a fast liquid chromatography method with diode-array detection and time-of-flight mass spectrometry. Rapid Commun Mass Spectrom 2009, 23, 3227-3242.
[22] Kumar, N., Singh, B., Gupta, A. P., Kaul, V. K., Lonijaposides, novel cerebrosides from Lonicera japonica. Tetrahedron 2006, 62, 4317-4322.
[23] Jian Yin, Ligong Guo, Modern Study of Chinese Drugs, Clinical Applications(7), Xueyuan Press, Beijing, 1993 (in Chinese).
[24] Yubin Ji (Chief Editor), Pharmacological Action, Application of Available Composition of Traditional Chinese Medicine, Heilongjiang Science and Technology Press, Heiiongjiang, 1995 (in Chinese).
[25] Jiangsu New Medical College, Chinese Medicine Dictionary, Shanghai Science and Technology Press, Shanghai, 1979 (in Chinese).
[26] Jingxi Xie, Wanzhi Song, Naigong Wang, JIU Ll XIANG. In Modern Studies of Chinese Herbal Medicine, Edited by Institute of Materia Medica, Chinese Academy of Medical Sciences, Union Press of Beijing Medical University and Peking Union Medical College, Beij
[27] Shilong Mao, Shixuan Liao, Jiuhong Wu, Huaqing Liang, Haisheng Chen, Cankun Zhang, APS, 1996,31(1),118-121.
[28] Jiaoshe Li, Yuying Zhao, Bin Wang, Xiulan Li, Libin Ma, APS, 1996, 31(11), 849-854.
[29] Ying Gu, Zhongda Huang, Yonghe Liu, APS, 1997, 32(1), 59-61.
[30] Dean Guo, Zhenggao Zhang, Guoqing Ye, Zhicen Lou, APS, 1997, 32(4), 282-285.
[31] Shilan Feng, Lan He, et al., CCMM, 1994, 19(10), 611-612.
[32] Enjuan Zhang, Qinshu Kang, Zhao Zhang, CCMM, 1993, 18(1), 37-38.
[33] Yong Ju, Mei Du, et al., CCMM, 1993, 18(10),611-613.
[34] Xianyi Zeng, Zhapu Fang, et al., CCMM, 1996, 21(3), 167-168.
[35] Yun Ling, Yonglin Zhang, et al., CCMM, 1998, 23(4), 232-233.
[36] Xifeng Huang, CCMM, 1997, 22(4),247-249.
[37] Wenji Sun, Jinfang Sneng, Brief Handbook of Natural Active Compounds, Medicinal Science and Technology Press of China, Beijing, 1998 (in Chinese).
[38] Chinese Materia Medica Editing Committee of the National Chinese Medicine, Pharmacology Bureau, Chinese Materia Medica (ZHONG HUA BEN CAO), Shanghai Science and Technology Press, Shanghai, 1999, Vols. 1-30 (in Chinese).
[39] Jiuhong Wu, Shixuan Liao, Shilong Mao, Yanghua Yi, Takeya K, Zhongwu Su, Chuanqing Lan, APS, 1999, 34(9), 682-685.
[40] Changxiang Chen, Weiwei Wang, Wei Ni, Nengyu Chen, Jun Zhou, ABY, 2000, 22(2), 201-208.
[41] Li Ji, et al., CCMM, 1990, 15(11), 680.