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30 articles for CJ Swain


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Cmpds
Data
Article Title
Organization
36
Novel 5-HT3 antagonists: indol-3-ylspiro(azabicycloalkane-3,5'(4'H)-oxazoles).EBI
Merck Sharp and Dohme Research Laboratories
49
Novel 5-HT3 antagonists. Indole oxadiazoles.EBI
Merck Sharp and Dohme Research Laboratories
7
An orally active, water-soluble neurokinin-1 receptor antagonist suitable for both intravenous and oral clinical administration.EBI
Merck
13
High affinity, selective neurokinin 2 and neurokinin 3 receptor antagonists from a common structural template.EBI
Merck Sharp Laboratory
14
 
3-Benzyloxy-2-phenylpiperidine NK1 antagonists: the influence of alpha methyl substitutionEBI
TBA
15
 
Piperidine-ether based hNK1 antagonists 2: Investigation of the effect of N-substitutionEBI
TBA
11
 
Phenyl-glycinol based NK1 receptor antagonists — towards the minimum pharmacophoreEBI
TBA
6
 
Quinuclidine-based NK1 antagonists, the role of the benzhydrylEBI
TBA
3
 
Gem-disubstituted amino-ether based substance p antagonistsEBI
TBA
5
 
Piperidine-ether based hNK1 antagonists 1: Determination of the relative and absolute stereochemical requirementsEBI
TBA
9
 
Acyclic NK1 antagonists: Replacements for the benzhydryl group.EBI
TBA
23
 
Acyclic NK-1 antagonists: 2-benzhydryl-2-aminoethyl ethersEBI
TBA
4
 
Quinuclidine based NK-1 antagonists 2: determination of the absolute stereochemical requirementsEBI
TBA
17
 
Quinuclidine-based NK-1 antagonists I: 3-benzyloxy-1-azabicyclo[2.2.2]octanesEBI
TBA
28
Identification and optimisation of 5-amino-7-aryldihydro-1,4-diazepines as 5-HT2A ligands.EBI
Merck Sharp and Dohme Research Laboratories
12
Novel lactam NK1 antagonists with anti-emetic activity.EBI
Merck Sharp & Dohme Research Laboratories
13
Synthesis and structure-activity relationships of 8-azabicyclo[3.2.1]octane benzylamine NK1 antagonists.EBI
Merck Sharp & Dohme Research Laboratories
10
Spirocyclic NK(1) antagonists II: [4.5]-spiroethers.EBI
Merck Sharp & Dohme Research Laboratories
19
Spirocyclic NK(1) antagonists I: [4.5] and [5.5]-spiroketals.EBI
Merck Sharp and Dohme Research Laboratories
16
4,4-Disubstituted cyclohexylamine NK(1) receptor antagonists II.EBI
Merck Sharp & Dohme Research Laboratories
19
4,4-Disubstituted cyclohexylamine NK(1) receptor antagonists I.EBI
Merck Sharp & Dohme Research Laboratories
19
2-Aryl indole NK(1) antagonists: optimisation of the amide substituent.EBI
Merck Sharp & Dohme Research Laboratories
27
2-Aryl indole NK1 receptor antagonists: optimisation of the 2-aryl ring and the indole nitrogen substituent.EBI
Merck Sharp and Dohme Research Laboratories
27
2-Aryl indole NK1 receptor antagonists: optimisation of indole substitution.EBI
The Neuroscience Research Centre
18
High affinity phenylglycinol-based NK1 receptor antagonists.EBI
Merck Sharp and Dohme Research Laboratories
37
4,4-Disubstituted piperidine high-affinity NK1 antagonists: structure-activity relationships and in vivo activity.EBI
Merck Sharp and Dohme Research Laboratories
11
N-heteroaryl-2-phenyl-3-(benzyloxy)piperidines: a novel class of potent orally active human NK1 antagonists.EBI
Merck Sharp and Dohme Research Laboratories
11
N-acyl-L-tryptophan benzyl esters: potent substance P receptor antagonists.EBI
Merck Sharp and Dohme Research Laboratories
31
Identification of L-tryptophan derivatives with potent and selective antagonist activity at the NK1 receptor.EBI
Merck Sharp and Dohme Research Laboratories
55
Identification of a series of 3-(benzyloxy)-1-azabicyclo[2.2.2]octane human NK1 antagonists.EBI
Merck Sharp and Dohme Research Laboratories