Endonuclease Inhibitors

(+)-15-epi Cloprostenol is a synthetic prostaglandin F2α (PGF2α) analog and a potent PGF2αR(FP receptor) agonist. The 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. When compared to 15(R)-cloprostenol, this epimer is less active by several

(+)-15-epi Cloprostenol is a synthetic prostaglandin F2α (PGF2α) analog and a potent PGF2αR(FP receptor) agonist. The 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. When compared to 15(R)-cloprostenol, this epimer is less active by several

(1S,2S)-1,2-di(naphthalen-2-yl)ethane-1,2-diamine.

(1S,2S)-1,2-di(naphthalen-2-yl)ethane-1,2-diamine.

(1S,2S)-1,2-di(naphthalen-2-yl)ethane-1,2-diamine.

(2S,4S)-8,9-diazatricyclo[4.3.0.0²⁴]nona-1(6),7-diene-7-carboxylic acid.

(2S,4S)-8,9-diazatricyclo[4.3.0.0²⁴]nona-1(6),7-diene-7-carboxylic acid.

(2S,4S)-8,9-diazatricyclo[4.3.0.0²⁴]nona-1(6),7-diene-7-carboxylic acid.

(2S,4S)-8,9-diazatricyclo[4.3.0.0²⁴]nona-1(6),7-diene-7-carboxylic acid.

(2S,4S)-8,9-diazatricyclo[4.3.0.0²⁴]nona-1(6),7-diene-7-carboxylic acid.

Reactant for preparation of: Topoisomerase I-targeting antitumor agents: C15-C21 stereopentad of discodermolide via cleavage of aminoglycosides, double-bond isomerization, and selective hydroxyl group protection: Diphenyl amine based sodium channel

Reactant for preparation of: Topoisomerase I-targeting antitumor agents: C15-C21 stereopentad of discodermolide via cleavage of aminoglycosides, double-bond isomerization, and selective hydroxyl group protection: Diphenyl amine based sodium channel