Molecular Biology Reagents

(S)-2-Pyridylthio Cysteamine Hydrochloride is a cleavable cross-linking reagent.

(S)-3,3'-Bis(4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol.

(S)-3,3'-Bis(4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol.

(S)-3,3'-Bis(4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol.

(S)-3,3'-Diiodo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene.

(S)-3-(Boc-amino)-4-(3-chlorophenyl)butyric acid.

(S)-3-(Boc-amino)-4-(3-chlorophenyl)butyric acid.

Applications：Useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens: and alkynylpyrimidine amide derivatives as orally available inhibitors of Tie-2 kinase.

Applications：Useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens: and alkynylpyrimidine amide derivatives as orally available inhibitors of Tie-2 kinase.

Applications：Useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens: and alkynylpyrimidine amide derivatives as orally available inhibitors of Tie-2 kinase.

Applications：Useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens: and alkynylpyrimidine amide derivatives as orally available inhibitors of Tie-2 kinase.

Applications：Useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens: and alkynylpyrimidine amide derivatives as orally available inhibitors of Tie-2 kinase.