Corynantheine (BioDeep_00000177675)
human metabolite blood metabolite natural product
代谢物信息卡片
化学式: C22H26N2O3 (366.1943)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(blood) 100%
分子结构信息
SMILES: C=CC1CN2CCc3c([nH]c4ccccc34)C2CC1C(=COC)C(=O)OC
InChI: InChI=1S/C22H26N2O3/c1-4-14-12-24-10-9-16-15-7-5-6-8-19(15)23-21(16)20(24)11-17(14)18(13-26-2)22(25)27-3/h4-8,13-14,17,20,23H,1,9-12H2,2-3H3
描述信息
同义名列表
7 个代谢物同义名
Methyl 2-{5-ethenyl-7,17-diazatetracyclo[8.7.0.0,.0,]heptadeca-1(10),11,13,15-tetraen-4-yl}-3-methoxyprop-2-enoic acid; Methyl 2-(3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)-3-methoxyprop-2-enoate; methyl 2-{3-ethenyl-1H,2H,3H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-2-yl}-3-methoxyprop-2-enoate; hirsuteine, (R-(R*,R*))-tartrate (1:1) salt; hirsuteine, (3beta,16E)-isomer; hirsuteine hydrochloride; Corynantheine
数据库引用编号
7 个数据库交叉引用编号
- ChEBI: CHEBI:181646
- PubChem: 3281521
- HMDB: HMDB0250477
- chemspider: 2530605
- LOTUS: LTS0048382
- LOTUS: LTS0120890
- wikidata: Q105268417
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)
13 个相关的物种来源信息
- 170017 - Corynanthe: LTS0048382
- 170031 - Corynanthe pachyceras: 10.1055/S-2000-8661
- 170031 - Corynanthe pachyceras: LTS0048382
- 2759 - Eukaryota: LTS0048382
- 9606 - Homo sapiens: -
- 3398 - Magnoliopsida: LTS0048382
- 292266 - Pseudocinchona: LTS0048382
- 640129 - Pseudocinchona pachyceras: 10.1055/S-2000-8661
- 640129 - Pseudocinchona pachyceras: LTS0048382
- 24966 - Rubiaceae: LTS0048382
- 35493 - Streptophyta: LTS0048382
- 58023 - Tracheophyta: LTS0048382
- 33090 - Viridiplantae: LTS0048382
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
- Hiroyuki Kitagawa, Masaya Munekage, Kengo Ichikawa, Ian Fukudome, Eri Munekage, Yuka Takezaki, Takashi Matsumoto, Yasushi Igarashi, Haruo Hanyu, Kazuhiro Hanazaki. Pharmacokinetics of Active Components of Yokukansan, a Traditional Japanese Herbal Medicine after a Single Oral Administration to Healthy Japanese Volunteers: A Cross-Over, Randomized Study.
PloS one.
2015; 10(7):e0131165. doi:
10.1371/journal.pone.0131165
. [PMID: 26151135] - Wen Qi, Si-Jia Yue, Jia-Hong Sun, James W Simpkins, Lin Zhang, Dan Yuan. Alkaloids from the hook-bearing branch of Uncariarhynchophylla and their neuroprotective effects against glutamate-induced HT22 cell death.
Journal of Asian natural products research.
2014; 16(8):876-83. doi:
10.1080/10286020.2014.918109
. [PMID: 24899363] - Takahiro Nakazawa, Koh-ichi Banba, Kazumasa Hata, Yutaka Nihei, Ayumi Hoshikawa, Keisuke Ohsawa. Metabolites of hirsuteine and hirsutine, the major indole alkaloids of Uncaria rhynchophylla, in rats.
Biological & pharmaceutical bulletin.
2006 Aug; 29(8):1671-7. doi:
10.1248/bpb.29.1671
. [PMID: 16880624] - Y Ozaki. [Vasodilative effects of indole alkaloids obtained from domestic plants, Uncaria rhynchophylla Miq. and Amsonia elliptica Roem. et Schult].
Nihon yakurigaku zasshi. Folia pharmacologica Japonica.
1990 Feb; 95(2):47-54. doi:
10.1254/fpj.95.2_47
. [PMID: 2328929]