IDAZOXAN (BioDeep_00001871443)
Main id: BioDeep_00000008418
代谢物信息卡片
IDAZOXAN
化学式: C11H12N2O2 (204.0898732)
中文名称: 亚达唑散
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1CN=C(N1)C2COC3=CC=CC=C3O2
InChI: InChI=1S/C11H12N2O2/c1-2-4-9-8(3-1)14-7-10(15-9)11-12-5-6-13-11/h1-4,10H,5-7H2,(H,12,13)
描述信息
C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C72900 - Adrenergic Antagonist
D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists
同义名列表
1 个代谢物同义名
数据库引用编号
10 个数据库交叉引用编号
- ChEBI: CHEBI:5862
- KEGG: C10968
- PubChem: 54459
- DrugBank: DB12551
- ChEMBL: CHEMBL10316
- MeSH: Idazoxan
- CAS: 84720-37-6
- CAS: 79944-58-4
- PubChem: 13151
- NIKKAJI: J33.875C
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)
0 个相关的物种来源信息
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
- Sònia Abás, Sergio Rodríguez-Arévalo, Andrea Bagán, Christian Griñán-Ferré, Foteini Vasilopoulou, Iria Brocos-Mosquera, Carolina Muguruza, Belén Pérez, Elies Molins, F Javier Luque, Pilar Pérez-Lozano, Steven de Jonghe, Dirk Daelemans, Lieve Naesens, José Brea, M Isabel Loza, Elena Hernández-Hernández, Jesús A García-Sevilla, M Julia García-Fuster, Milica Radan, Teodora Djikic, Katarina Nikolic, Mercè Pallàs, Luis F Callado, Carmen Escolano. Bicyclic α-Iminophosphonates as High Affinity Imidazoline I2 Receptor Ligands for Alzheimer's Disease.
Journal of medicinal chemistry.
2020 04; 63(7):3610-3633. doi:
10.1021/acs.jmedchem.9b02080. [PMID: 32150414] - M Julia García-Fuster, Jesús A García-Sevilla. Effects of anti-depressant treatments on FADD and p-FADD protein in rat brain cortex: enhanced anti-apoptotic p-FADD/FADD ratio after chronic desipramine and fluoxetine administration.
Psychopharmacology.
2016 Aug; 233(15-16):2955-71. doi:
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Brain structure & function.
2016 06; 221(5):2703-15. doi:
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Zhonghua wei zhong bing ji jiu yi xue.
2016 May; 28(5):445-9. doi:
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Drug and alcohol dependence.
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Metabolism: clinical and experimental.
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2009 May; 84(19-20):696-704. doi:
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2008 Jul; 36(7):1385-405. doi:
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Experimental physiology.
2007 Sep; 92(5):923-31. doi:
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2007 Jan; 25(1):147-55. doi:
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Neuroscience.
2006 Sep; 142(1):21-8. doi:
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2006 Mar; 96(6):1551-9. doi:
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2006 Feb; 96(4):1111-20. doi:
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The Journal of neuroscience : the official journal of the Society for Neuroscience.
2006 Jan; 26(2):467-78. doi:
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Clinical and experimental pharmacology & physiology.
2004 May; 31(5-6):348-53. doi:
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2004 Apr; 24(2):150-4. doi:
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2004 Mar; 18(1):47-53. doi:
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2002 Oct; 453(2-3):287-97. doi:
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American journal of physiology. Heart and circulatory physiology.
2002 Jun; 282(6):H2336-45. doi:
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2002 Jun; 42(7):958-65. doi:
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American journal of physiology. Renal physiology.
2002 May; 282(5):F943-52. doi:
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2002 May; 97(1-2):117-25. doi:
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European journal of pharmacology.
2002 Jan; 435(1):19-26. doi:
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