Heliamine (BioDeep_00000007392)
Secondary id: BioDeep_00001868903
natural product Volatile Flavor Compounds
代谢物信息卡片
化学式: C11H15NO2 (193.110273)
中文名称: 6,7-二甲氧基-1,2,3,4-四氢异喹啉
谱图信息:
最多检出来源 Escherichia coli(natural_products) 33.33%
分子结构信息
SMILES: COC(C(OC)=C1)=CC2=C1CNCC2
InChI: InChI=1S/C11H15NO2/c1-13-10-5-8-3-4-12-7-9(8)6-11(10)14-2/h5-6,12H,3-4,7H2,1-2H3
描述信息
An isoquinoline that is 1,2,3,4-tetrahydroisoquinoline substituted by methoxy groups at positions 6 and 7.
同义名列表
数据库引用编号
16 个数据库交叉引用编号
- ChEBI: CHEBI:5637
- KEGG: C09460
- PubChem: 15623
- Metlin: METLIN67718
- ChEMBL: CHEMBL12367
- CAS: 1745-07-9
- MoNA: CCMSLIB00005436068
- PMhub: MS000020736
- MetaboLights: MTBLC5637
- PubChem: 11651
- KNApSAcK: C00001865
- 3DMET: B02988
- NIKKAJI: J263.656E
- RefMet: Heliamine
- KNApSAcK: 5637
- LOTUS: LTS0062875
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)
23 个相关的物种来源信息
- 41773 - Berberidaceae: LTS0062875
- 22774 - Berberis: LTS0062875
- 258147 - Berberis canadensis: 10.1007/BF00631016
- 1112794 - Berberis integerrima: 10.1007/BF00631016
- 1112794 - Berberis integerrima: LTS0062875
- 121720 - Berberis thunbergii: 10.1007/BF02254817
- 121720 - Berberis thunbergii: LTS0062875
- 3593 - Cactaceae: LTS0062875
- 171968 - Carnegiea: LTS0062875
- 171969 - Carnegiea gigantea: 10.1021/NP50021A008
- 171969 - Carnegiea gigantea: LTS0062875
- 2759 - Eukaryota: LTS0062875
- 3398 - Magnoliopsida: LTS0062875
- 154434 - Pachycereus: LTS0062875
- 223066 - Pachycereus militaris: 10.1002/JPS.2600690127
- 223066 - Pachycereus militaris: 10.1021/NP50016A021
- 154438 - Pachycereus weberi:
- 154438 - Pachycereus weberi: 10.1016/0031-9422(80)87036-1
- 154438 - Pachycereus weberi: 10.1021/AC00279A030
- 154438 - Pachycereus weberi: LTS0062875
- 35493 - Streptophyta: LTS0062875
- 58023 - Tracheophyta: LTS0062875
- 33090 - Viridiplantae: LTS0062875
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
- Kambarali K Turgunov, Sherzod N Zhurakulov, Ulli Englert, Valentina I Vinogradova, Bakhodir Tashkhodjaev. Synthesis of 2-(2-hydroxyethyl)-1-(2-hydroxyphenyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline and pseudosymmetry in its crystal structure.
Acta crystallographica. Section C, Structural chemistry.
2016 Aug; 72(Pt 8):607-11. doi:
10.1107/s2053229616010792. [PMID: 27487334] - Ken-ichi Umehara, Kouichi Wada, Kiyoshi Noguchi, Takafumi Iwatsubo, Takashi Usui, Hidetaka Kamimura. Relationship between exposure of (-)-N-{2-[(R)-3-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)piperidino]ethyl}-4-fluorobenzamide (YM758), a 'funny' if current channel inhibitor, and heart rate reduction in tachycardia-induced beagle dogs.
Drug metabolism and disposition: the biological fate of chemicals.
2009 Jul; 37(7):1427-33. doi:
10.1124/dmd.108.026385. [PMID: 19359407] - Nicola A Colabufo, Francesco Berardi, Maria Grazia Perrone, Mariangela Cantore, Marialessandra Contino, Carmela Inglese, Mauro Niso, Roberto Perrone. Multi-drug-resistance-reverting agents: 2-aryloxazole and 2-arylthiazole derivatives as potent BCRP or MRP1 inhibitors.
ChemMedChem.
2009 Feb; 4(2):188-95. doi:
10.1002/cmdc.200800329. [PMID: 19140144] - R Mata, J L McLaughlin. Cactus alkaloids XLII: 3,4-dimethoxy-beta-phenethylamine and heliamine from the Mexican cereoid Backebergia militaris.
Journal of pharmaceutical sciences.
1980 Jan; 69(1):94-5. doi:
10.1002/jps.2600690127. [PMID: 7354455]