Dibenzylamine (BioDeep_00000178198)
human metabolite blood metabolite
代谢物信息卡片
化学式: C14H15N (197.120443)
中文名称: 二苄胺
谱图信息:
最多检出来源 Homo sapiens(blood) 20.87%
分子结构信息
SMILES: C(NCC1=CC=CC=C1)C1=CC=CC=C1
InChI: InChI=1S/C14H15N/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10,15H,11-12H2
描述信息
同义名列表
数据库引用编号
5 个数据库交叉引用编号
- ChEBI: CHEBI:189125
- PubChem: 7656
- HMDB: HMDB0251169
- ChEMBL: CHEMBL3182419
- CAS: 103-49-1
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)
1 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
- Peter Urbanovský, Jan Kotek, Fabio Carniato, Mauro Botta, Petr Hermann. Lanthanide Complexes of DO3A-(Dibenzylamino)methylphosphinate: Effect of Protonation of the Dibenzylamino Group on the Water-Exchange Rate and the Binding of Human Serum Albumin.
Inorganic chemistry.
2019 Apr; 58(8):5196-5210. doi:
10.1021/acs.inorgchem.9b00267
. [PMID: 30942072] - Paul E Harrington, David J St Jean, Jeffrey Clarine, Thomas S Coulter, Michael Croghan, Adam Davenport, James Davis, Chiara Ghiron, Jonathan Hutchinson, Michael G Kelly, Fred Lott, Jenny Ying-Lin Lu, David Martin, Sean Morony, Steve F Poon, Elena Portero-Larragueta, Jeff D Reagan, Kelly A Regal, Andrew Tasker, Minghan Wang, Yuhua Yang, Guomin Yao, Qingping Zeng, Charles Henley, Christopher Fotsch. The discovery of an orally efficacious positive allosteric modulator of the calcium sensing receptor containing a dibenzylamine core.
Bioorganic & medicinal chemistry letters.
2010 Sep; 20(18):5544-7. doi:
10.1016/j.bmcl.2010.07.060
. [PMID: 20708930] - Bach Dinh, Kevin Dove, Dilara Jappar, Joseph A Hrabie, Keith M Davies. Effect of hydrophobic structure on the catalysis of nitric oxide release from zwitterionic diazeniumdiolates in surfactant and liposome media.
Nitric oxide : biology and chemistry.
2005 Nov; 13(3):204-9. doi:
10.1016/j.niox.2005.07.003
. [PMID: 16122951] - Satyanarayana Sreemantula, Krishna M Boini, Srinivas Nammi. Reserpine methonitrate, a novel quaternary analogue of reserpine augments urinary excretion of VMA and 5-HIAA without affecting HVA in rats.
BMC pharmacology.
2004 Nov; 4(?):30. doi:
10.1186/1471-2210-4-30
. [PMID: 15546495] - Jose S Santos, Dong-Kuk Lee, Ayyalusamy Ramamoorthy. Effects of antidepressants on the conformation of phospholipid headgroups studied by solid-state NMR.
Magnetic resonance in chemistry : MRC.
2004 Feb; 42(2):105-14. doi:
10.1002/mrc.1327
. [PMID: 14745789] - M B Calvo, J L Pedraz, A Domínguez-Gil. Pharmacokinetics of dibenzylamine administered in a sustained drug delivery system with cefazolin.
Biopharmaceutics & drug disposition.
1990 Dec; 11(9):797-806. doi:
10.1002/bdd.2510110907
. [PMID: 2271755] - M B Calvo, J L Pedraz, A Domínguez-Gil. Determination of low concentrations of dibenzylamine in human plasma and urine by gas chromatography with a nitrogen-phosphorus detector.
Journal of chromatography.
1989 May; 490(1):206-12. doi:
10.1016/s0378-4347(00)82776-0
. [PMID: 2760151] - U CONSBRUCH, C FAUST. [Comparative longitudinal section observation of serum protein ratios in exogenous traumatic psychoses and endogenous psychoses after treatment with reserpine, iminodibenzyl derivative and phenothiazines].
Archiv fur Psychiatrie und Nervenkrankheiten, vereinigt mit Zeitschrift fur die gesamte Neurologie und Psychiatrie.
1958; 197(3):279-87. doi:
10.1007/bf00394685
. [PMID: 13595861] - U CONSBRUCH, C FAUST. [Comparative cross-sectional studies of serum protein conditions in exogenous traumatic psychoses & endogenous psychoses treated with reserpine, iminodibenzyl derivatives & phenothiazines].
Confinia neurologica.
1958; 18(2-4):280-3. doi:
NULL
. [PMID: 13597508]