2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine
                             
                            
                            
                                
                            
                            
                                
                            
                            
                            
                                
                                    
                                            
	"2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, 
	MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, 
	which enables searching at various levels of specificity.
	
	
		
			
			
				A selective D1 dopamine receptor agonist used primarily as a research tool.
    
			
			
				
				
					
						| Descriptor ID | D015647 | 
					
						| MeSH Number(s) | D03.633.100.079.800 | 
					
						| Concept/Terms | 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine1H-3-Benzazepine-7,8-diol, 2,3,4,5-tetrahydro-1-phenyl-
 SK&F-38393SK&F-38393SK&F 38393SK&F38393SKF38393SKF-38393SKF 38393R-SK&F 38393RSK&F 38393SKF 38393-ASKF 38393 ASKF 38393A
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				Below are MeSH descriptors whose meaning is more general than "2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine" by people in this website by year, and whether "2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine" was a major or minor topic of these publications. 
				
					 
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		            | Year | Major Topic | Minor Topic | Total | 
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| 2000 | 0 | 1 | 1 | 
| 2001 | 0 | 1 | 1 | 
| 2002 | 0 | 1 | 1 | 
| 2003 | 2 | 2 | 4 | 
| 2004 | 0 | 1 | 1 | 
| 2005 | 0 | 2 | 2 | 
| 2006 | 0 | 3 | 3 | 
| 2007 | 0 | 3 | 3 | 
| 2008 | 0 | 1 | 1 | 
| 2009 | 0 | 1 | 1 | 
| 2010 | 0 | 2 | 2 | 
| 2012 | 0 | 2 | 2 | 
| 2013 | 0 | 1 | 1 | 
| 2019 | 0 | 1 | 1 | 
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				Below are the most recent publications written about "2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine" by people in Profiles.
						
					
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								Injection of D1 receptor antagonist SCH23390 into the periaqueductal gray attenuates morphine withdrawal symptoms in rats. Neurosci Lett. 2020 01 01; 714:134502. 
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								Kidney dopamine D1-like receptors and angiotensin 1-7 interaction inhibits renal Na+ transporters. Am J Physiol Renal Physiol. 2019 10 01; 317(4):F949-F956. 
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								Rhodium-catalyzed asymmetric addition of arylboronic acids to ?-nitroolefins: formal synthesis of (S)-SKF 38393. Org Lett. 2013 Nov 15; 15(22):5730-3. 
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								Transcription factor Nrf2 protects renal dopamine D1 receptor function during oxidative stress. Hypertension. 2013 Sep; 62(3):512-7. 
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								Altered functioning of both renal dopamine D1 and angiotensin II type 1 receptors causes hypertension in old rats. Hypertension. 2012 May; 59(5):1029-36. 
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								Novel role of NF-?B-p65 in antioxidant homeostasis in human kidney-2 cells. Am J Physiol Renal Physiol. 2012 Jun 01; 302(11):F1440-6. 
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								Oxidative stress alters renal D1 and AT1 receptor functions and increases blood pressure in old rats. Am J Physiol Renal Physiol. 2011 Jan; 300(1):F133-8. 
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								Exercise reduces oxidative stress but does not alleviate hyperinsulinemia or renal dopamine D1 receptor dysfunction in obese rats. Am J Physiol Renal Physiol. 2011 Jan; 300(1):F98-104. 
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								Exercise activates redox-sensitive transcription factors and restores renal D1 receptor function in old rats. Am J Physiol Renal Physiol. 2009 Nov; 297(5):F1174-80. 
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								Renal proximal tubules from old Fischer 344 rats grow into epithelial cells in cultures and exhibit increased oxidative stress and reduced D1 receptor function. Am J Physiol Cell Physiol. 2008 Nov; 295(5):C1326-31.