Uvangoletin (BioDeep_00000022917)

human metabolite

代谢物信息卡片

Uvangoletin

化学式: C16H16O4 (272.1048536)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=CC(=CC(=C1C(=O)CCC2=CC=CC=C2)O)O
InChI: InChI=1S/C16H16O4/c1-20-15-10-12(17)9-14(19)16(15)13(18)8-7-11-5-3-2-4-6-11/h2-6,9-10,17,19H,7-8H2,1H3

描述信息

同义名列表

1 个代谢物同义名

Uvangoletin

数据库引用编号

5 个数据库交叉引用编号

ChEBI: CHEBI:180160
PubChem: 6483649
HMDB: HMDB0132914
ChEMBL: CHEMBL4641401
PMhub: MS000097087

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)

8 个相关的物种来源信息

864332 - Cedrelopsis grevei: 10.1016/S0031-9422(02)00675-1
191066 - Empetrum nigrum: 10.1111/J.1438-8677.1992.TB00302.X
9606 - Homo sapiens: -
130418 - Piper umbellatum: 10.1248/YAKUSHI.122.291
92927 - Sarcandra glabra: 10.1016/0031-9422(96)00352-4
260143 - Syzygium samarangense: 10.1055/S-2004-835859
672960 - Uvaria acuminata:
672961 - Uvaria angolensis:

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

Junyi Shen, Xinrui Zhu, Zhenru Wu, Yujun Shi, Tianfu Wen. Uvangoletin, extracted from Sarcandra glabra, exerts anticancer activity by inducing autophagy and apoptosis and inhibiting invasion and migration on hepatocellular carcinoma cells. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2022 Jan; 94(?):153793. doi: 10.1016/j.phymed.2021.153793. [PMID: 34736000]
Yanping Zhang, Taohua Yuan, Yunsong Li, Ning Wu, Xiaotian Dai. Network Pharmacology Analysis of the Mechanisms of Compound Herba Sarcandrae (Fufang Zhongjiefeng) Aerosol in Chronic Pharyngitis Treatment. Drug design, development and therapy. 2021; 15(?):2783-2803. doi: 10.2147/dddt.s304708. [PMID: 34234411]
Gasper Maeda, Jelle van der Wal, Arvind Kumar Gupta, Joan J E Munissi, Andreas Orthaber, Per Sunnerhagen, Stephen S Nyandoro, Máté Erdélyi. Oxygenated Cyclohexene Derivatives and Other Constituents from the Roots of Monanthotaxis trichocarpa. Journal of natural products. 2020 02; 83(2):210-215. doi: 10.1021/acs.jnatprod.9b00363. [PMID: 31986029]
Tian-Yin Liu, Shi-Biao Chen. Sarcandra glabra combined with lycopene protect rats from lipopolysaccharide induced acute lung injury via reducing inflammatory response. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2016 Dec; 84(?):34-41. doi: 10.1016/j.biopha.2016.09.009. [PMID: 27631138]
Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont, Sanan Subhadhirasakul, Supinya Tewtrakul. Anti-HIV-1 protease activity of compounds from Boesenbergia pandurata. Bioorganic & medicinal chemistry. 2006 Mar; 14(6):1710-4. doi: 10.1016/j.bmc.2005.10.019. [PMID: 16263298]
Momoyo Ichimaru, Noriyoshi Nakatani, Tomoko Takahashi, Yumi Nishiyama, Masataka Moriyasu, Atsushi Kato, Simon G Mathenge, Francis D Juma, Joseph N Nganga. Cytotoxic C-benzylated dihydrochalcones from Uvaria acuminata. Chemical & pharmaceutical bulletin. 2004 Jan; 52(1):138-41. doi: 10.1248/cpb.52.138. [PMID: 14709883]
Takahiko Isobe, Ayumi Ohsaki, Kumiko Nagata. [Antibacterial constituents against Helicobacter pylori of Brazilian medicinal plant, Pariparoba]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan. 2002 Apr; 122(4):291-4. doi: 10.1248/yakushi.122.291. [PMID: 11968842]