Roseoside (BioDeep_00000269519)
natural product
代谢物信息卡片
化学式: C19H30O8 (386.194058)
中文名称: 长寿花糖甙
谱图信息:
最多检出来源 Lycium chinense(natural_products) 33.33%
分子结构信息
SMILES: CC([C@@](/C=C/[C@H](O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)C)(O)C(C)(C)C2)=CC2=O
InChI: InChI=1S/C19H30O8/c1-10-7-12(21)8-18(3,4)19(10,25)6-5-11(2)26-17-16(24)15(23)14(22)13(9-20)27-17/h5-7,11,13-17,20,22-25H,8-9H2,1-4H3/b6-5+/t11-,13-,14-,15+,16-,17-,19-/m1/s1
描述信息
D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids
同义名列表
数据库引用编号
5 个数据库交叉引用编号
- PubChem: 9930064
- ChEMBL: CHEMBL482383
- KNApSAcK: C00029329
- CAS: 54835-70-0
- MoNA: CCMSLIB00000579260
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)
1 个相关的物种来源信息
- 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
- Fatma Kübra Ata, Fahriye Ercan, Serap Yalcin Azarkan. In vivo, in vitro and Molecular Modelling Analysis of Isoquercetin, Roseoside, Coreximine, Anonaine, and Arianacin Molecules.
Current computer-aided drug design.
2022; 18(3):168-184. doi:
10.2174/1573409918666220509213313
. [PMID: 35538817] - Taylan B Morcol, Konrad Wysocki, Renuka P Sankaran, Paul D Matthews, Edward J Kennelly. UPLC-QTof-MSE Metabolomics Reveals Changes in Leaf Primary and Secondary Metabolism of Hop (Humulus lupulus L.) Plants under Drought Stress.
Journal of agricultural and food chemistry.
2020 Dec; 68(49):14698-14708. doi:
10.1021/acs.jafc.0c05987
. [PMID: 33236890] - Zhi-Gang Wu, Wei Wei, Hai-Yan Xu, Lin-Lin Zheng, Chao-Mei Ma, Ying-Chun Wang. Constituents from the Leaves of Tetraena mongolica and Their Protective Activity in HEK 293t Cells Damaged by CdCl2.
Journal of natural products.
2019 10; 82(10):2707-2712. doi:
10.1021/acs.jnatprod.9b00212
. [PMID: 31593459] - Silvia Revoltella, Bettina Rainer, Birgit Waltenberger, Konrad Pagitz, Stefan Schwaiger, Hermann Stuppner. HPTLC Autography Based Screening and Isolation of Mushroom Tyrosinase Inhibitors of European Plant Species.
Chemistry & biodiversity.
2019 Mar; 16(3):e1800541. doi:
10.1002/cbdv.201800541
. [PMID: 30556957] - Janggyoo Choi, Kee Dong Yoon, Jinwoong Kim. Chemical constituents from Taraxacum officinale and their α-glucosidase inhibitory activities.
Bioorganic & medicinal chemistry letters.
2018 02; 28(3):476-481. doi:
10.1016/j.bmcl.2017.12.014
. [PMID: 29254644] - Nguyen Phuong Thao, Bui Thi Thuy Luyen, Le Ba Vinh, Jung Yun Lee, Young In Kwon, Young Ho Kim. Rat intestinal sucrase inhibited by minor constituents from the leaves and twigs of Archidendron clypearia (Jack.) Nielsen.
Bioorganic & medicinal chemistry letters.
2016 09; 26(17):4272-6. doi:
10.1016/j.bmcl.2016.07.044
. [PMID: 27481560] - Mamdouh Nabil Samy, Ashraf Nageeb El-Sayed Hamed, Sachiko Sugimoto, Hideaki Otsuka, Mohamed Salah Kamel, Katsuyoshi Matsunami. Officinalioside, a new lignan glucoside from Borago officinalis L.
Natural product research.
2016; 30(8):967-72. doi:
10.1080/14786419.2015.1088540
. [PMID: 26382913] - Xiang-xi Yi, Cheng-hai Gao, Bin Long, Zhi-wei Su, Lian Yu, Bi-juan He. [Study on Chemical Constituents from Hypocotyls of Mangrove Bruguiera gymnorrhiza].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2015 Jan; 38(1):85-8. doi:
. [PMID: 26214874]
- N Z Mamadalieva, F Sharopov, J-P Girault, M Wink, R Lafont. Phytochemical analysis and bioactivity of the aerial parts of Abutilon theophrasti (Malvaceae), a medicinal weed.
Natural product research.
2014; 28(20):1777-9. doi:
10.1080/14786419.2014.939080
. [PMID: 25050787] - Ngoc Vinh Huynh, Thi Hoai Thu Nguyen, Kim Phi Phung Nguyen, Poul Erik Hansen. Structural studies of the chemical constituents of Tithonia tagetiflora Desv. (Asteraceae).
Magnetic resonance in chemistry : MRC.
2013 Jul; 51(7):439-43. doi:
10.1002/mrc.3963
. [PMID: 23681665] - Jie Ma, Jianbo Yang, Tengfei Ji, Aiguo Wang, Yalun Su. [Chemical constituents from Hypericum perforatum].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2012 Aug; 37(16):2408-12. doi:
10.4268/cjcmm20121613
. [PMID: 23234139] - Neil Frankish, Fábio de Sousa Menezes, Clive Mills, Helen Sheridan. Enhancement of insulin release from the beta-cell line INS-1 by an ethanolic extract of Bauhinia variegata and its major constituent roseoside.
Planta medica.
2010 Jul; 76(10):995-7. doi:
10.1055/s-0029-1240868
. [PMID: 20143296] - Tzong-Huei Lee, Guei-Jane Wang, Ching-Kuo Lee, Yueh-Hsiung Kuo, Chang-Hung Chou. Inhibitory effects of glycosides from the leaves of Melaleuca quinquenervia on vascular contraction of rats.
Planta medica.
2002 Jun; 68(6):492-6. doi:
10.1055/s-2002-32563
. [PMID: 12094289] - Hideyuki Ito, Eri Kobayashi, Shu-Hua Li, Tsutomu Hatano, Daigo Sugita, Naoki Kubo, Susumu Shimura, Yoshio Itoh, Harukuni Tokuda, Hoyoku Nishino, Takashi Yoshida. Antitumor activity of compounds isolated from leaves of Eriobotrya japonica.
Journal of agricultural and food chemistry.
2002 Apr; 50(8):2400-3. doi:
10.1021/jf011083l
. [PMID: 11929303] - Y Murai, S Kashimura, S Tamezawa, T Hashimoto, S Takaoka, Y Asakawa, K Kiguchi, F Murai, M Tagawa. Absolute configuration of (6S,9S)-roseoside from Polygonum hydropiper.
Planta medica.
2001 Jul; 67(5):480-1. doi:
10.1055/s-2001-15812
. [PMID: 11488470]