Tulipalin B (BioDeep_00000013905)

natural product

代谢物信息卡片

2(3H)-Furanone, dihydro-4-hydroxy-3-methylene-

化学式: C5H6O3 (114.0316926)
中文名称:
谱图信息: 最多检出来源 Viridiplantae(plant) 10.55%

分子结构信息

SMILES: C=C1C(=O)OCC1O
InChI: InChI=1S/C5H6O3/c1-3-4(6)2-8-5(3)7/h4,6H,1-2H2/t4-/m0/s1

描述信息

A member of the class of butan-4-olides that is 3-methylidenebutan-4-olide carrying an additional hydroxy substituent at position 4 (the 4R-enantiomer)

同义名列表

2 个代谢物同义名

Tulipalin B; 2(3H)-Furanone, dihydro-4-hydroxy-3-methylene-

数据库引用编号

9 个数据库交叉引用编号

ChEBI: CHEBI:87123
KEGG: C21187
PubChem: 5318286
PubChem: 162351
CAS: 38965-80-9
PMhub: MS000028488
MetaboLights: MTBLC87123
PubChem: 315431310
LOTUS: LTS0051414

分类词条

Terpenoids

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)

42 个相关的物种来源信息

2759 - Eukaryota: LTS0051414
4677 - Liliaceae: LTS0051414
4447 - Liliopsida: LTS0051414
3398 - Magnoliopsida: LTS0051414
35493 - Streptophyta: LTS0051414
58023 - Tracheophyta: LTS0051414
13305 - Tulipa: 10.1111/J.1600-0536.1999.TB06080.X
13305 - Tulipa: LTS0051414
1155211 - Tulipa agenensis: 10.1111/J.1600-0536.1999.TB06080.X
1155211 - Tulipa agenensis: LTS0051414
468982 - Tulipa biflora: 10.1111/J.1600-0536.1999.TB06080.X
468982 - Tulipa biflora: LTS0051414
344607 - Tulipa clusiana: 10.1111/J.1600-0536.1999.TB06080.X
344607 - Tulipa clusiana: LTS0051414
13306 - Tulipa gesneriana:
1155216 - Tulipa humilis: 10.1111/J.1600-0536.1999.TB06080.X
1155216 - Tulipa humilis: LTS0051414
2173071 - Tulipa kaufmanniana: 10.1111/J.1600-0536.1999.TB06080.X
2173071 - Tulipa kaufmanniana: LTS0051414
1200331 - Tulipa linifolia: 10.1111/J.1600-0536.1999.TB06080.X
1200331 - Tulipa linifolia: LTS0051414
1137804 - Tulipa montana: LTS0051414
2173066 - Tulipa patens: 10.1111/J.1600-0536.1999.TB06080.X
2173066 - Tulipa patens: LTS0051414
1218738 - Tulipa praestans: 10.1111/J.1600-0536.1999.TB06080.X
1218738 - Tulipa praestans: LTS0051414
248498 - Tulipa sylvestris: 10.1016/S0031-9422(98)00716-X
248498 - Tulipa sylvestris: 10.1111/J.1600-0536.1999.TB06080.X
248498 - Tulipa sylvestris: LTS0051414
202164 - Tulipa tarda: 10.1111/J.1600-0536.1999.TB06080.X
202164 - Tulipa tarda: LTS0051414
89494 - Tulipa turkestanica:
89494 - Tulipa turkestanica: 10.1016/S0031-9422(98)00716-X
89494 - Tulipa turkestanica: 10.1080/09168451.2014.946395
89494 - Tulipa turkestanica: 10.1111/J.1600-0536.1999.TB06080.X
89494 - Tulipa turkestanica: 10.1271/BBB.130663
89494 - Tulipa turkestanica: LTS0051414
1155219 - Tulipa undulatifolia: 10.1111/J.1600-0536.1999.TB06080.X
1155219 - Tulipa undulatifolia: LTS0051414
662770 - Tulipa urumiensis: 10.1111/J.1600-0536.1999.TB06080.X
662770 - Tulipa urumiensis: LTS0051414
33090 - Viridiplantae: LTS0051414

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

Taiji Nomura, Ayaka Ueno, Shinjiro Ogita, Yasuo Kato. Molecular diversity of tuliposide B-converting enzyme in tulip (Tulipa gesneriana): identification of the root-specific isozyme. Bioscience, biotechnology, and biochemistry. 2017 Jun; 81(6):1185-1193. doi: 10.1080/09168451.2017.1295806. [PMID: 28485211]
Taiji Nomura, Tatsunori Murase, Shinjiro Ogita, Yasuo Kato. Molecular identification of tuliposide B-converting enzyme: a lactone-forming carboxylesterase from the pollen of tulip. The Plant journal : for cell and molecular biology. 2015 Jul; 83(2):252-62. doi: 10.1111/tpj.12883. [PMID: 25997073]
Taiji Nomura, Emiko Hayashi, Shohei Kawakami, Shinjiro Ogita, Yasuo Kato. Environmentally benign process for the preparation of antimicrobial α-methylene-β-hydroxy-γ-butyrolactone (tulipalin B) from tulip biomass. Bioscience, biotechnology, and biochemistry. 2015; 79(1):25-35. doi: 10.1080/09168451.2014.946395. [PMID: 25126881]
Kengo Shigetomi, Kazuaki Shoji, Shinya Mitsuhashi, Makoto Ubukata. The antibacterial properties of 6-tuliposide B. Synthesis of 6-tuliposide B analogues and structure-activity relationship. Phytochemistry. 2010 Feb; 71(2-3):312-24. doi: 10.1016/j.phytochem.2009.10.008. [PMID: 19939419]