Vanilloloside (BioDeep_00000022263)
human metabolite Endogenous natural product
代谢物信息卡片
化学式: C14H20O8 (316.1158)
中文名称:
谱图信息:
最多检出来源 Salix miyabeana(not specific) 4.88%
分子结构信息
SMILES: COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O
InChI: InChI=1S/C14H20O8/c1-20-9-4-7(5-15)2-3-8(9)21-14-13(19)12(18)11(17)10(6-16)22-14/h2-4,10-19H,5-6H2,1H3
描述信息
Vanilloloside is found in herbs and spices. Vanilloloside is isolated from unripe vanilla pod.
Isolated from unripe vanilla pods. Vanilloloside is found in herbs and spices.
同义名列表
18 个代谢物同义名
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)-2-methoxyphenoxy]oxane-3,4,5-triol; 4-(Hydroxymethyl)-2-methoxyphenyl beta-D-glucopyranoside; 4-(Hydroxymethyl)-2-methoxyphenyl β-D-glucopyranoside; Vanillyl alcohol 4-O-beta-D-glucopyranoside; Vanillyl alcohol 4-O-β-D-glucopyranoside; SCHEMBL4545342; Vanilloloside; .BETA.-D-GLUCOPYRANOSIDE, 4-(HYDROXYMETHYL)-2-METHOXYPHENYL; (2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(4-(hydroxymethyl)-2-methoxy-phenoxy)tetrahydropyran-3,4,5-triol; (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-(hydroxymethyl)-2-methoxyphenoxy)tetrahydro-2H-pyran-3,4,5-triol; 4-(beta-D-glucopyranosyloxy)-3-methoxybenzyl alcohol; 4-(HYDROXYMETHYL)-2-METHOXYPHENYL .BETA.-D-GLUCOPYRANOSIDE; beta-D-Glucopyranoside, 4-(hydroxymethyl)-2-methoxyphenyl; Glucovanillyl alcohol; SIMPNXWTAVEOTO-RKQHYHRCSA-N; UNII-UU9VCO3B28; UU9VCO3B28; VANILLYL ALCOHOL 4-O-.BETA.-D-GLUCOPYRANOSIDE
数据库引用编号
12 个数据库交叉引用编号
- ChEBI: CHEBI:68967
- PubChem: 44577222
- PubChem: 69086659
- HMDB: HMDB0032013
- ChEMBL: CHEMBL468568
- KNApSAcK: C00032471
- foodb: FDB008711
- chemspider: 24695215
- CAS: 74950-96-2
- PMhub: MS000081897
- RefMet: Vanilloloside
- LOTUS: LTS0157289
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)
74 个相关的物种来源信息
- 4022 - Acer: LTS0157289
- 4024 - Acer saccharum: 10.1021/NP200678N
- 4024 - Acer saccharum: LTS0157289
- 4037 - Apiaceae: LTS0157289
- 4210 - Asteraceae: LTS0157289
- 24079 - Bignoniaceae: LTS0157289
- 301453 - Capparaceae: LTS0157289
- 13394 - Capparis: 10.1021/NP9006298
- 13394 - Capparis: LTS0157289
- 16737 - Chloranthaceae: LTS0157289
- 3954 - Combretaceae: LTS0157289
- 37818 - Dendrobium: LTS0157289
- 142614 - Dendrobium moniliforme: 10.1021/NP0301801
- 142614 - Dendrobium moniliforme: LTS0157289
- 2759 - Eukaryota: LTS0157289
- 21496 - Gentiana: LTS0157289
- 21472 - Gentianaceae: LTS0157289
- 9606 - Homo sapiens: -
- 629714 - Hypericaceae: LTS0157289
- 55962 - Hypericum: LTS0157289
- 282539 - Hypericum erectum: 10.1007/S11418-008-0256-X
- 282539 - Hypericum erectum: LTS0157289
- 179730 - Itoa: LTS0157289
- 179731 - Itoa orientalis: 10.1021/NP800014S
- 179731 - Itoa orientalis: LTS0157289
- 190523 - Laguncularia: LTS0157289
- 190524 - Laguncularia racemosa: 10.1016/J.PHYTOCHEM.2009.11.008
- 190524 - Laguncularia racemosa: LTS0157289
- 4136 - Lamiaceae: LTS0157289
- 4447 - Liliopsida: LTS0157289
- 26468 - Loganiaceae: LTS0157289
- 3398 - Magnoliopsida: LTS0157289
- 50767 - Metagentiana rhodantha: 10.1002/CBDV.201000220
- 4430 - Nelumbo: LTS0157289
- 4432 - Nelumbo nucifera: 10.1248/BPB.33.267
- 4432 - Nelumbo nucifera: LTS0157289
- 4429 - Nelumbonaceae: LTS0157289
- 4747 - Orchidaceae: LTS0157289
- 68553 - Phellodendron: LTS0157289
- 68554 - Phellodendron amurense: 10.1016/S0031-9422(00)90536-3
- 68554 - Phellodendron amurense: LTS0157289
- 40958 - Pimpinella: LTS0157289
- 271192 - Pimpinella anisum: 10.1016/S0031-9422(03)00179-1
- 271192 - Pimpinella anisum: LTS0157289
- 23513 - Rutaceae: LTS0157289
- 3688 - Salicaceae: LTS0157289
- 23672 - Sapindaceae: LTS0157289
- 13669 - Sarcandra: LTS0157289
- 92927 - Sarcandra glabra: 10.1016/J.FITOTE.2009.12.009
- 92927 - Sarcandra glabra: LTS0157289
- 41629 - Saussurea: LTS0157289
- 137893 - Saussurea medusa: 10.1016/S0968-0896(02)00470-4
- 137893 - Saussurea medusa: LTS0157289
- 4139 - Scutellaria: LTS0157289
- 1907919 - Scutellaria albida: LTS0157289
- 2200782 - Scutellaria albida subsp. albida: 10.1016/J.PHYTOCHEM.2007.04.014
- 2200782 - Scutellaria albida subsp. albida: LTS0157289
- 509705 - Soroseris: LTS0157289
- 996406 - Soroseris hookeriana: 10.1055/S-2000-8607
- 996406 - Soroseris hookeriana: LTS0157289
- 260324 - Stereospermum: 10.1016/J.PHYTOCHEM.2005.10.009
- 260324 - Stereospermum: LTS0157289
- 1818594 - Stereospermum cylindricum: 10.1016/J.PHYTOCHEM.2005.10.009
- 1818594 - Stereospermum cylindricum: LTS0157289
- 35493 - Streptophyta: LTS0157289
- 26496 - Strychnos: 10.1016/J.PHYTOCHEM.2007.12.002
- 26496 - Strychnos: LTS0157289
- 1037789 - Strychnos axillaris: 10.1016/J.PHYTOCHEM.2007.12.002
- 1037789 - Strychnos axillaris: LTS0157289
- 58023 - Tracheophyta: LTS0157289
- 51238 - Vanilla: LTS0157289
- 51239 - Vanilla planifolia: 10.1002/PCA.2800050108
- 51239 - Vanilla planifolia: LTS0157289
- 33090 - Viridiplantae: LTS0157289
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。
亚细胞结构定位 | 关联基因列表 |
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文献列表
- Tao Yuan, Chunpeng Wan, Antonio González-Sarrías, Vamsikrishna Kandhi, Nadja B Cech, Navindra P Seeram. Phenolic glycosides from sugar maple (Acer saccharum) bark.
Journal of natural products.
2011 Nov; 74(11):2472-6. doi:
10.1021/np200678n
. [PMID: 22032697] - Xing Yun Chai, Yue Lin Song, Zheng Ren Xu, Hai Ming Shi, Chang Cai Bai, Dan Bi, Jing Wen, Fei Fei Li, Peng Fei Tu. Itosides J-N from Itoa orientalis and structure - anti-COX-2 activity relationship of phenolic glycosides.
Journal of natural products.
2008 May; 71(5):814-9. doi:
10.1021/np800014s
. [PMID: 18412396] - Hideki Kanho, Sayaka Yaoya, Nobuo Kawahara, Takahisa Nakane, Yoichi Takase, Kazuo Masuda, Masanori Kuroyanagi. Biotransformation of benzaldehyde-type and acetophenone-type derivatives by Pharbitis nil hairy roots.
Chemical & pharmaceutical bulletin.
2005 Apr; 53(4):361-5. doi:
10.1248/cpb.53.361
. [PMID: 15802832] - Chunsheng Zhao, Qunfang Liu, Fathi Halaweish, Baoping Shao, Yuqing Ye, Weimin Zhao. Copacamphane, picrotoxane, and alloaromadendrane sesquiterpene glycosides and phenolic glycosides from Dendrobium moniliforme.
Journal of natural products.
2003 Aug; 66(8):1140-3. doi:
10.1021/np0301801
. [PMID: 12932145]