Liriodendrin (BioDeep_00000230592)
Secondary id: BioDeep_00000000366, BioDeep_00000003806
PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C34H46O18 (742.2684016000001)
中文名称: (-)-丁香树脂醇二葡萄糖甙, 丁香树脂醇双葡萄糖苷, 丁香脂素二葡萄糖苷, 刺五加苷E, 刺五加苷D, 刺五加苷 D, 刺五加甙 E
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 19.18%
分子结构信息
SMILES: COC(C=C1[C@H]2[C@@](CO[C@@H]3C4=CC(OC)=C(O[C@@H]([C@@H]([C@@H](O)[C@@H]5O)O)O[C@@H]5CO)C(OC)=C4)([H])[C@]3([H])CO2)=C(C(OC)=C1)O[C@@H]([C@@H]([C@@H](O)[C@@H]6O)O)O[C@@H]6CO
InChI: InChI=1S/C34H46O18/c1-43-17-5-13(6-18(44-2)31(17)51-33-27(41)25(39)23(37)21(9-35)49-33)29-15-11-48-30(16(15)12-47-29)14-7-19(45-3)32(20(8-14)46-4)52-34-28(42)26(40)24(38)22(10-36)50-34/h5-8,15-16,21-30,33-42H,9-12H2,1-4H3
描述信息
(-)-syringaresinol O,O-bis(beta-D-glucoside) is a beta-D-glucoside that is the 4,4-bis(beta-D-glucosyl) derivative of (-)-syringaresinol. It has a role as a plant metabolite, an antioxidant and an anti-inflammatory agent. It is functionally related to a (-)-syringaresinol.
Acanthoside D is a natural product found in Crescentia cujete, Daphne giraldii, and other organisms with data available.
A beta-D-glucoside that is the 4,4-bis(beta-D-glucosyl) derivative of (-)-syringaresinol.
Eleutheroside E is an important component of Acanthopanax, which has anti-inflammatory and protective effects on ischemic heart.
Eleutheroside E is an important component of Acanthopanax, which has anti-inflammatory and protective effects on ischemic heart.
Syringaresinol diglucoside is a natural compound from bamboo leaves[1].
Syringaresinol diglucoside is a natural compound from bamboo leaves[1].
同义名列表
16 个代谢物同义名
(2S,3R,4S,5S,6R)-2-[4-[(3R,3aS,6R,6aS)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol; (7beta,7beta,8beta,8beta)-4,4-bis(beta-D-glucopyranosyloxy)-3,3,5,5-tetramethoxy-7,9:7,9-diepoxylignan; (-)-syringaresinol O,O-bis(beta-D-glucoside); (-)-Syringaresinol di-beta-D-glucoside; (-)-Syringaresinol di-O-glucoside; (-)-Syringaresinol diglucoside; Syringaresinol-di-O-glucoside; Syringaresinol diglucoside; (-)-Syringaresinol; Acanthoside D; Liriodendrin; 2-{4-[4-(3,5-dimethoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2,6-dimethoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol; 2-Bromo-3-nitrobenzoic acid; Eleutheroside D; Eleutheroside E; Acanthoside D
数据库引用编号
27 个数据库交叉引用编号
- ChEBI: CHEBI:2375
- KEGG: C10543
- PubChem: 442830
- PubChem: 226371
- PubChem: 13245166
- Metlin: METLIN91550
- Wikipedia: Liriodendrin
- MeSH: acanthoside D
- chemspider: 66297
- CAS: 66791-77-3
- CAS: 79484-75-6
- CAS: 39432-56-9
- CAS: 96038-87-8
- CAS: 573-44-4
- medchemexpress: HY-N1958
- PMhub: MS000169617
- PMhub: MS000152682
- MetaboLights: MTBLC2375
- PubChem: 12726
- 3DMET: B03942
- NIKKAJI: J405.567E
- medchemexpress: HY-N0272
- LOTUS: LTS0016790
- KNApSAcK: 2375
- LOTUS: LTS0011685
- wikidata: Q103818952
- LOTUS: LTS0249935
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
114 个相关的物种来源信息
- 3813 - Albizia julibrissin: 10.1248/CPB.40.829
- 13336 - Annona: LTS0016790
- 49314 - Annona cherimola: 10.1002/JCCS.199800095
- 49314 - Annona cherimola: LTS0016790
- 22140 - Annonaceae: LTS0016790
- 4056 - Apocynaceae: LTS0016790
- 4050 - Araliaceae: LTS0016790
- 40552 - Asparagaceae: LTS0016790
- 99295 - Breynia: LTS0016790
- 283133 - Breynia androgyna: LTS0016790
- 87753 - Cistanche: LTS0016790
- 161397 - Cistanche tubulosa: 10.1248/CPB.38.1927
- 161397 - Cistanche tubulosa: LTS0016790
- 401068 - Coleogyne: LTS0016790
- 401069 - Coleogyne ramosissima: 10.1016/S0031-9422(00)00192-8
- 401069 - Coleogyne ramosissima: LTS0016790
- 66679 - Daphne: LTS0016790
- 2753873 - Daphne feddei: 10.1021/NP8004166
- 2753873 - Daphne feddei: LTS0016790
- 885948 - Daphne tangutica: 10.1016/J.FITOTE.2009.07.002
- 50304 - Eleutherococcus: LTS0016790
- 265764 - Eleutherococcus gracilistylus: 10.1007/S11418-011-0509-Y
- 50305 - Eleutherococcus nodiflorus: 10.1007/S11418-011-0509-Y
- 82096 - Eleutherococcus senticosus: 10.1007/S10600-011-9773-Z
- 82096 - Eleutherococcus senticosus: 10.1055/S-2001-18352
- 82096 - Eleutherococcus senticosus: 10.1055/S-2008-1074537
- 82096 - Eleutherococcus senticosus: 10.1248/CPB.38.1763
- 82096 - Eleutherococcus senticosus: LTS0016790
- 105886 - Eleutherococcus sessiliflorus:
- 2026872 - Eria mucronata:
- 2759 - Eukaryota: LTS0016790
- 2759 - Eukaryota: LTS0249935
- 3977 - Euphorbiaceae: LTS0016790
- 3803 - Fabaceae: LTS0016790
- 25168 - Galium: LTS0016790
- 69062 - Globularia: LTS0016790
- 1533088 - Globularia alypum: 10.1002/HLCA.19810640103
- 1533088 - Globularia alypum: LTS0016790
- 4321 - Icacinaceae: LTS0016790
- 162809 - Inga: LTS0016790
- 124960 - Iodes: LTS0016790
- 1705841 - Iodes cirrhosa: 10.1021/NP7007329
- 1705841 - Iodes cirrhosa: LTS0016790
- 4136 - Lamiaceae: LTS0016790
- 4136 - Lamiaceae: LTS0249935
- 22788 - Lardizabalaceae: LTS0016790
- 41707 - Lawsonia: LTS0016790
- 141191 - Lawsonia inermis: 10.1016/J.BMCL.2010.06.118
- 141191 - Lawsonia inermis: LTS0016790
- 4447 - Liliopsida: LTS0016790
- 43170 - Linaria: LTS0016790
- 43171 - Linaria vulgaris: 10.1248/CPB.50.1393
- 43171 - Linaria vulgaris: LTS0016790
- 3413 - Liriodendron: LTS0016790
- 3415 - Liriodendron tulipifera: 10.1021/JO01096A007
- 3415 - Liriodendron tulipifera: LTS0016790
- 26468 - Loganiaceae: LTS0016790
- 45193 - Luehea: LTS0016790
- 3928 - Lythraceae: LTS0016790
- 3402 - Magnolia: LTS0016790
- 85854 - Magnolia coco: 10.1021/NP970571D
- 85854 - Magnolia coco: LTS0016790
- 3401 - Magnoliaceae: LTS0016790
- 3398 - Magnoliopsida: LTS0016790
- 3398 - Magnoliopsida: LTS0249935
- 20202 - Mallotus: LTS0016790
- 396487 - Mallotus macrostachyus: 10.1016/J.PHYTOL.2011.07.007
- 396487 - Mallotus macrostachyus: LTS0016790
- 3629 - Malvaceae: LTS0016790
- 15970 - Nolina: LTS0016790
- 191664 - Nolina microcarpa: 10.1007/BF00630606
- 191664 - Nolina microcarpa: LTS0016790
- 4144 - Oleaceae: LTS0016790
- 91896 - Orobanchaceae: LTS0016790
- 4054 - Panax ginseng: 10.1248/CPB.55.1291
- 69923 - Penstemon: LTS0016790
- 160368 - Penstemon deustus: 10.1021/JO01295A038
- 160368 - Penstemon deustus: LTS0016790
- 316257 - Phlomis: LTS0016790
- 316257 - Phlomis: LTS0249935
- 997702 - Phlomis aurea: 10.1016/S0031-9422(00)00331-9
- 997702 - Phlomis aurea: LTS0016790
- 997702 - Phlomis aurea: LTS0249935
- 233880 - Phyllanthaceae: LTS0016790
- 156152 - Plantaginaceae: LTS0016790
- 33090 - Plants: -
- 52847 - Plumeria: LTS0016790
- 62097 - Plumeria rubra: 10.1021/NP50072A008
- 62097 - Plumeria rubra: LTS0016790
- 306974 - Porcelia: LTS0016790
- 3745 - Rosaceae: LTS0016790
- 24966 - Rubiaceae: LTS0016790
- 50505 - Sargentodoxa: LTS0016790
- 50506 - Sargentodoxa cuneata: 10.1016/J.PHYTOCHEM.2005.09.018
- 50506 - Sargentodoxa cuneata: 10.3987/COM-03-9777
- 50506 - Sargentodoxa cuneata: LTS0016790
- 212320 - Sauropus: LTS0016790
- 283133 - Sauropus androgynus: 10.1016/S0031-9422(03)00219-X
- 35493 - Streptophyta: LTS0016790
- 35493 - Streptophyta: LTS0249935
- 26496 - Strychnos: LTS0016790
- 1037789 - Strychnos axillaris: 10.1016/J.PHYTOCHEM.2007.12.002
- 1037789 - Strychnos axillaris: LTS0016790
- 24208 - Syringa: LTS0016790
- 126367 - Syringa reticulata: 10.1016/J.BMCL.2011.08.089
- 126367 - Syringa reticulata: LTS0016790
- 39987 - Thymelaeaceae: LTS0016790
- 58023 - Tracheophyta: LTS0016790
- 58023 - Tracheophyta: LTS0249935
- 33090 - Viridiplantae: LTS0016790
- 33090 - Viridiplantae: LTS0249935
- 3971 - Viscum: 10.1055/S-2007-969090
- 33090 - 大血藤: -
- 569774 - 金线莲: -
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Peng Du, Mingdao Lei, Yu Liu, Shilin Yang. Simultaneous Determination and Pharmacokinetic Study of Six Components in Rat Plasma by HPLC-MS/MS after Oral Administration of Acanthopanax sessiliflorus Fruit Extract.
International journal of molecular sciences.
2016 Dec; 18(1):. doi:
10.3390/ijms18010045
. [PMID: 28036026] - Soo-Yeon Park, Gyeong-Min Do, Sena Lee, Yeni Lim, Jae-Ho Shin, Oran Kwon. Acanthopanax divaricatus var. chiisanensis reduces blood pressure via the endothelial nitric oxide synthase pathway in the spontaneously hypertensive rat model.
Nutrition research (New York, N.Y.).
2014 Sep; 34(9):797-806. doi:
10.1016/j.nutres.2014.08.013
. [PMID: 25241331] - Longshan Zhao, Qi An, Feng Qin, ZhiLi Xiong. Simultaneous determination of six constituents in the fruit of Acanthopanax sessiliflorus (Rupr. et Maxim.) Seem. by HPLC-UV.
Natural product research.
2014; 28(7):500-2. doi:
10.1080/14786419.2013.877904
. [PMID: 24438013] - Eun-Jung Lim, Gyeong-Min Do, Jae-Ho Shin, Oran Kwon. Protective effects of Acanthopanax divaricatus vat. albeofructus and its active compound on ischemia-reperfusion injury of rat liver.
Biochemical and biophysical research communications.
2013 Mar; 432(4):599-605. doi:
10.1016/j.bbrc.2013.02.039
. [PMID: 23453782] - Dioni A da Silva, Vanessa G Alves, Danielle M M Franco, Laryssa C Ribeiro, Maria C de Souza, Lucilia Kato, João E de Carvalho, Luciana K Kohn, Cecília M A de Oliveira, Cleuza C da Silva. Antiproliferative activity of Luehea candicans Mart. et Zucc. (Tiliaceae).
Natural product research.
2012; 26(4):364-9. doi:
10.1080/14786411003752102
. [PMID: 21432719] - Chu Van Men, Yu Seon Jang, Kwan Jun Lee, Jae Hyun Lee, Tran Hong Quang, Nguyen Van Long, Hoang Van Luong, Young Ho Kim, Jong Seong Kang. Multiple component quantitative analysis for the pattern recognition and quality evaluation of Kalopanacis Cortex using HPLC.
Archives of pharmacal research.
2011 Dec; 34(12):2065-71. doi:
10.1007/s12272-011-1209-6
. [PMID: 22210032] - Huan-Kai Yao, Jing-Yu Duan, Yan Li, Jian-Hui Wang, Xiao-Xing Yin, Hong-Quan Duan. [Studies on the chemical constituents from the roots of Kalopanax septemlobus].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2011 May; 34(5):716-8. doi:
. [PMID: 21954557]
- A R Gohari, S Saeidnia, M Bayati-Moghadam, Gh Amin. Lignans and neolignans from Stelleropsis antoninae.
Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences.
2011; 19(1):74-9. doi:
. [PMID: 22615643]
- Rakhi Srivastava, Daman Saluja, Bilikere S Dwarakanath, Madhu Chopra. Inhibition of Human Cervical Cancer Cell Growth by Ethanolic Extract of Boerhaavia diffusa Linn. (Punarnava) Root.
Evidence-based complementary and alternative medicine : eCAM.
2011; 2011(?):427031. doi:
10.1093/ecam/nep223
. [PMID: 21869896] - Chun Feng, Bo-Gang Li, Xiao-Ping Gao, Hua-Yi Qi, Guo-Lin Zhang. A new triterpene and an antiarrhythmic liriodendrin from Pittosporum brevicalyx.
Archives of pharmacal research.
2010 Dec; 33(12):1927-32. doi:
10.1007/s12272-010-1206-1
. [PMID: 21191756] - Tomoko Sano, Ikue Matsumura, Rie Nakamura, Hiroki Yamaji, Kazunori Hashimoto, Osami Takeda, Fumiyuki Kiuchi, Tadahiro Takeda. Genetic and chemical comparison of Boi (Sinomeni Caulis et Rhizoma) and Seifuto (Caulis Sinomenii).
Journal of natural medicines.
2010 Jul; 64(3):257-65. doi:
10.1007/s11418-010-0397-6
. [PMID: 20217263] - Sonia A Tucci, Emma J Boyland, Jason Cg Halford. The role of lipid and carbohydrate digestive enzyme inhibitors in the management of obesity: a review of current and emerging therapeutic agents.
Diabetes, metabolic syndrome and obesity : targets and therapy.
2010 May; 3(?):125-43. doi:
10.2147/dmsott.s7005
. [PMID: 21437083] - Zhi-jing Ma, Zhi-juan Zhao. [Studies on chemical constituents from stem barks of Fraxinus paxiana].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2008 Aug; 33(16):1990-3. doi:
"
. [PMID: 19086636] - Li-Guang Zhou, Xue-Song Feng, Kai-Yi Huang, Le He, Xu-Ming Deng, Da-Cheng Wang. [Studies on chemical constituents of Syringa veutina].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2008 May; 31(5):679-81. doi:
. [PMID: 18826143]
- Maoluo Gan, Yanling Zhang, Sheng Lin, Mingtao Liu, Weixia Song, Jiachen Zi, Yongchun Yang, Xiaona Fan, Jiangong Shi, Jinfeng Hu, Jiandong Sun, Naihong Chen. Glycosides from the root of Iodes cirrhosa.
Journal of natural products.
2008 Apr; 71(4):647-54. doi:
10.1021/np7007329
. [PMID: 18327912] - Yu Xiang, You-Bin Li, Jian Zhang, Ping Li, Yuan-Zhang Yao. [Studies on chemical constituents of Salsola collina].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2007 Mar; 32(5):409-13. doi:
. [PMID: 17511147]
- Jia-Ming Sun, Jun-Shan Yang, Hui Zhang. Two new flavanone glycosides of Jasminum lanceolarium and their anti-oxidant activities.
Chemical & pharmaceutical bulletin.
2007 Mar; 55(3):474-6. doi:
10.1248/cpb.55.474
. [PMID: 17329896] - X Yang, Y Ding, Z-H Sun, D-M Zhang. Studies on chemical constituents from Ilex pubescens.
Journal of Asian natural products research.
2006 Sep; 8(6):505-10. doi:
10.1080/10286020500176344
. [PMID: 16931425] - Jian-fei Chao, Zhi-qi Yin, Wen-cai Ye, Shou-xun Zhao. [Chemical constituents from branch of Broussonetia papyrifera].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2006 Jul; 31(13):1078-80. doi:
"
. [PMID: 17048607] - Hyun-Ju Jung, Hee-Juhn Park, Ryung-Gue Kim, Kyoung-Min Shin, Joohun Ha, Jong-Won Choi, Hyoung Ja Kim, Yong Sup Lee, Kyung-Tae Lee. In vivo anti-inflammatory and antinociceptive effects of liriodendrin isolated from the stem bark of Acanthopanax senticosus.
Planta medica.
2003 Jul; 69(7):610-6. doi:
10.1055/s-2003-41127
. [PMID: 12898415] - Huiming Hua, Maosheng Cheng, Xian Li, Yuehu Pei. A new pyrroloquinazoline alkaloid from Linaria vulgaris.
Chemical & pharmaceutical bulletin.
2002 Oct; 50(10):1393-4. doi:
10.1248/cpb.50.1393
. [PMID: 12372872] - Gang-li Wang, Hua Yan, Qing-yun Hou, Yang Lu, Ning-bo Gong, Rui-chao Lin. [Chemical constituents from Alyxia sinensis (II)].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2002 Mar; 27(3):199-201. doi:
"
. [PMID: 12774400] - I Caliş, H Kirmizibekmez, O Sticher. Iridoid glycosides from Globularia trichosantha.
Journal of natural products.
2001 Jan; 64(1):60-4. doi:
10.1021/np0003591
. [PMID: 11170667]