Skip to main navigation
Skip to search
Skip to main content
Sort by
Pharmacology, Toxicology and Pharmaceutical Science
Vanilloid Receptor 1 Antagonist
100%
Capsaicin
88%
Structure Activity Relationship
80%
Vanilloid Receptor 1
58%
Receptor
50%
G Protein Coupled Receptor
48%
Resiniferatoxin
32%
Rat
30%
Nucleoside
28%
Carboxamide
27%
S Adenosylhomocysteine
26%
Adenosylhomocysteinase
26%
Alzheimer's Disease
26%
Pyridine
26%
Analgesic Agent
24%
Thiourea
22%
Reduced Nicotinamide Adenine Dinucleotide Phosphate Oxidase
20%
IC50
19%
Chinese Hamster
19%
Vasculotropin
19%
Antitumor Activity
18%
Neuropathic Pain
17%
Hypothermia
17%
Dimer
17%
Nucleic Acid Base
17%
Antiangiogenic
17%
Reactive Oxygen Metabolite
17%
Binding Site
15%
Phosphotransferase
15%
Osteoclast Differentiation Factor
14%
Partial Agonist
14%
4 Aminobutyric Acid
14%
Quantitative Structure-Activity Relationship
14%
Janus Kinase
14%
Aminotransferase
13%
Acetamide Derivative
13%
Albumin
13%
Quantitative Structure Activity Relation
13%
Comparative Molecular Field Analysis
13%
Anticarcinogen
13%
Computer-Aided Drug Design
13%
Hydrogen
13%
Phthalocyanine
13%
Neoplasm
13%
Malignant Neoplasm
12%
Adenosine A3 Receptor Antagonist
12%
Janus Kinase 1
12%
Combinatorial Library
12%
Enzymes
11%
Adenosine Receptor Ligands
11%
Biochemistry, Genetics and Molecular Biology
G Protein Coupled Receptor
56%
Enzyme
40%
TRPV1
28%
Agonist
28%
Active Site
26%
Transient Receptor Potential Vanilloid
26%
Cyclase
26%
Structure Activity Relation
26%
Hydrolase
25%
Drug Development
23%
Crystal Structure
23%
Molecular Model
22%
S-Adenosyl-L-Homocysteine
22%
Adenosine A2A Receptor
21%
Peptide
20%
DNA Template
18%
Arginine
17%
Isoform
16%
G Protein
15%
Antineoplastic Activity
15%
Amyloid Protein
14%
X Ray
14%
Nucleoside
14%
Signal Transduction
13%
Electric Potential
13%
N-Terminus
11%
Binding Site
11%
Homology Modeling
11%
Nucleobase
11%
Pharmacophore
10%
NAD(P)H Oxidase
10%
Thiourea
10%
Anticancer
9%
Gamma-Aminobutyric Acid
9%
Binding Affinity
8%
Adenosine Receptor Antagonist
8%
Adenosine Receptor Agonist
8%
Vibrio vulnificus
8%
Plasmodium falciparum
8%
Protein Structure Prediction
8%
Pyridoxal Phosphate
8%
Receptor Tyrosine Kinase
8%
Cytochrome P450 Inhibitor
8%
Cytochrome P450
8%
Reductase
8%
Tyrosine Kinase
8%
Calpain
8%
Enzymatic Activity
8%
Transaminase
8%
Oxidoreductase
8%
Chemistry
Structure-Activity Relationship
49%
Capsaicin
43%
Inhibition Constant (Ki)
32%
Pyridine
31%
Nucleobase
22%
Vanilloid
22%
Kd
18%
Stereoselective Synthesis
17%
Nucleoside
16%
Peptide
16%
Antineoplastic Agent
14%
Adenosine A3 Receptor Agonist
13%
D-Ribose
13%
Lactone
13%
Cycloaddition
13%
Natural Product
13%
Adenosine
12%
Thioadenosine
12%
Antitumor
12%
Hydrogen Bonding
12%
Hydrophobic Interaction
11%
Carboxamide
11%
Lead Compound
11%
Amino Group
10%
Antiallodynic
8%
Condensation Reaction
8%
Heterocyclic Compound
8%
D-Gulonic Acid
8%
Quinolone
8%
Pyrrolopyrimidine
8%
D-Mannose
8%
Nucleophilic Aromatic Substitution
8%
Asymmetric Synthesis
8%
Fluorination
8%
Cytosine
8%
Triazole
8%
Nucleophilic Substitution
8%
Alkaloid Synthesis
8%
Catalyst
8%
Density Functional Theory Study
8%
Urea
8%
Molecular Dynamics Simulation
8%
Pentapeptide
8%
Acetamide
8%
Partial Agonist
8%
Bioactivity
8%
Diastereoselectivity
8%
Selenium
7%
Alkaloid
7%
Michael Addition
7%
