Medicine & Life Sciences
luminamicin
100%
Ether
28%
3-hydroxybutanal
28%
Trehalose
21%
Tunicamycin
20%
Anti-Bacterial Agents
20%
imidazo(1,2-c)pyrimidine
19%
irumamycin
19%
tunicaminyluracil
18%
mureidomycin A
18%
furan
17%
Lactones
16%
2-(7-(3,4-dimethoxyphenyl)imidazo(1,2-c)pyrimidin-5-ylamino)nicotinamide
16%
Biological Products
15%
Maleic Anhydrides
15%
decalin
14%
undecane
14%
Germinal Center Kinases
14%
Polyprenols
14%
Aldehydes
13%
N,N-diacetylchitobiose
13%
phosphatidylinositol mannoside
13%
C 27
13%
Acetals
13%
Cyanates
13%
C-Type Lectins
13%
Cycloaddition Reaction
12%
muramyl-NAc-(pentapeptide)pyrophosphoryl-undecaprenol
12%
Uridine Diphosphate N-Acetylglucosamine
12%
Solid-Phase Synthesis Techniques
12%
Ethers
12%
Palladium
11%
Acids
11%
Syk Kinase
11%
Nucleosides
10%
Lipids
10%
indole
10%
pyridine
10%
Dipeptides
10%
Solubility
9%
Cross Reactions
9%
Amides
9%
Inositol
8%
Alkaloids
8%
Glycosylation
7%
Skeleton
7%
Dichlorodiphenyldichloroethane
7%
lipid I
7%
Urea
7%
Glycolipids
6%
Chemical Compounds
Total Synthesis
50%
Lipid
24%
Macrolactonization
23%
Tunicamycin
23%
Glycerolipid
23%
Antimicrobial Agent
21%
Tensyuic Acid B
18%
Ethynyl
18%
Brartemicin
16%
Mureidomycin A
16%
Polyprenol Phosphate
15%
Ether
15%
Cross-Coupling Reaction
15%
Glycolipid
15%
Maleic Anhydride
15%
Lactone
14%
Phosphatidylinositol Mannoside
14%
Enol Ether
14%
imidazo[1,2-c]pyrimidine
14%
Aromatic Structure
13%
Hydrostannylation
13%
Antibacterial
12%
Lectin
12%
Cis-Decalin
11%
Occurrence in Nature
11%
Mukaiyama Aldol Addition
11%
Stille Cross Coupling
11%
Undecane
10%
Cyanate
10%
Structure-Activity Relationship
9%
Lipid As
9%
Stille Reaction
9%
Phosphotransferase Inhibitor
9%
Trehalose
9%
Nucleoside
9%
Oxidative Elimination Reaction
9%
Chemical Depolymerization
9%
Vinyl Group
8%
Tensyuic Acid
8%
Diester
8%
Brown
8%
Molecule
8%
Aldehyde
8%
Glycosylation
7%
Acetal
7%
Dipole
7%
Biological Property
7%
Furan
7%
Agonist
7%
Indole
7%