Trispheridine (BioDeep_00000009155)

代谢物信息卡片

Trisphaeridine

化学式: C14H9NO2 (223.0633254)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: c1ccc2c(c1)c1cc3c(cc1cn2)OCO3
InChI: InChI=1S/C14H9NO2/c1-2-4-12-10(3-1)11-6-14-13(16-8-17-14)5-9(11)7-15-12/h1-7H,8H2

描述信息

同义名列表

2 个代谢物同义名

Trisphaeridine; Trispheridine

数据库引用编号

11 个数据库交叉引用编号

ChEBI: CHEBI:32266
KEGG: C12182
PubChem: 443684
Metlin: METLIN69349
ChEMBL: CHEMBL511443
KNApSAcK: C00029148
CAS: 224-11-3
PMhub: MS000022904
PubChem: 14328
NIKKAJI: J673.498G
RefMet: Trisphaeridine

分类词条

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)

20 个相关的物种来源信息

164437 - Crinum americanum: 10.1016/S0031-9422(00)81704-5
205937 - Crinum asiaticum: 10.1016/0031-9422(90)80023-A
573716 - Crinum firmifolium: 10.1016/0031-9422(95)00565-X
209099 - Crinum latifolium: 10.1021/NP030529K
112538 - Crinum yemense: 10.1021/NP030529K
527298 - Cyrtanthus obliquus: 10.1016/S0031-9422(02)00206-6
146421 - Eucharis amazonica: 10.1002/CHIN.200334195
82232 - Galanthus elwesii: 10.1016/J.PHYTOCHEM.2003.12.013
197690 - Galanthus gracilis: 10.1055/S-1999-14062
51448 - Galanthus plicatus: 10.1007/BF00568518
1263218 - Hippeastrum morelianum: 10.1002/MRC.2794
1234392 - Hippeastrum puniceum: 10.3390/MOLECULES16087097
59040 - Hymenocallis littoralis: 10.1016/0031-9422(95)00372-E
112565 - Lapiedra martinezii: 10.1016/0031-9422(90)80157-C
54835 - Leucojum aestivum: 10.1021/NP800585C
54837 - Narcissus asturiensis: 10.1055/S-2006-957781
54860 - Narcissus tazetta: 10.1002/CBDV.201400309
644807 - Pancratium maritimum: 10.1515/ZNC-2004-1-214
1055008 - Pancratium trianthum:
82257 - Zephyranthes candida: 10.1021/NP3005425

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

Ogbole Omonike Oluyemisi, Ajaiyeoba Edith Oriabure, Adeniji J Adekunle, Kamdem Soup T Ramsay, Sajan Shyyaula, Muhammad Iqbal Choudhary. Bioassay-guided isolation of Poliovirus-inhibiting constituents from Zephyranthes candida. Pharmaceutical biology. 2015 Jun; 53(6):882-7. doi: 10.3109/13880209.2014.946061. [PMID: 25431196]
Sabrin R M Ibrahim, Gamal A Mohamed, Lamiaa A Shaala, Diaa T A Youssef, Khalid A El Sayed. New alkaloids from Pancratium maritimum. Planta medica. 2013 Oct; 79(15):1480-4. doi: 10.1055/s-0033-1350741. [PMID: 23970422]
Simone A Baechler, Markus Fehr, Michael Habermeyer, Andreas Hofmann, Karl-Heinz Merz, Heinz-Herbert Fiebig, Doris Marko, Gerhard Eisenbrand. Synthesis, topoisomerase-targeting activity and growth inhibition of lycobetaine analogs. Bioorganic & medicinal chemistry. 2013 Feb; 21(3):814-23. doi: 10.1016/j.bmc.2012.11.011. [PMID: 23266176]
Jian-Sai Yang, Xu Feng, Yu Chen, Xing-Zeng Zhao, Ming Wang, Qi-Zhi Wang, Yun-Fa Dong. [Study on the chemical constituents from the bulbs of Zephyranthes candida]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2010 Nov; 33(11):1730-2. doi: . [PMID: 21434434]
István Zupkó, Borbála Réthy, Judit Hohmann, Joseph Molnár, Imre Ocsovszki, George Falkay. Antitumor activity of alkaloids derived from Amaryllidaceae species. In vivo (Athens, Greece). 2009 Jan; 23(1):41-8. doi: . [PMID: 19368123]
László Szlávik, Agnes Gyuris, János Minárovits, Peter Forgo, József Molnár, Judit Hohmann. Alkaloids from Leucojum vernum and antiretroviral activity of Amaryllidaceae alkaloids. Planta medica. 2004 Sep; 70(9):871-3. doi: 10.1055/s-2004-827239. [PMID: 15386196]
Judit Hohmann, Peter Forgo, Joseph Molnár, Krisztina Wolfard, Annamária Molnár, Theresia Thalhammer, Imre Máthé, Derek Sharples. Antiproliferative amaryllidaceae alkaloids isolated from the bulbs of Sprekelia formosissima and Hymenocallis x festalis. Planta medica. 2002 May; 68(5):454-7. doi: 10.1055/s-2002-32068. [PMID: 12058326]