Chemical Synthesis

Application(3-Trimethylsilyl-2-propynyl)triphenylphosphonium Bromide has been used in the synthesis of olefinic peptides that exhibit renin inhibitor activity against both hog kidney renin and human amniotic renin.

Application(3-Trimethylsilyl-2-propynyl)triphenylphosphonium Bromide has been used in the synthesis of olefinic peptides that exhibit renin inhibitor activity against both hog kidney renin and human amniotic renin.

(4-Bromobenzyl)triphenylphosphonium Bromide.

(4-Bromobenzyl)triphenylphosphonium Bromide.

(4-Bromobenzyl)triphenylphosphonium Bromide.

(4-Bromobenzyl)triphenylphosphonium Bromide.

Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells Reactant for preparation of: Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions Methyl alkenyl

Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells Reactant for preparation of: Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions Methyl alkenyl

Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells Reactant for preparation of: Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions Methyl alkenyl

Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells Reactant for preparation of: Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions Methyl alkenyl

Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells Reactant for preparation of: Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions Methyl alkenyl

application：Reactant for the synthesis of:β-amyloid plaque ligandsSelective norbornane-type aspartate analog inhibitors of glutamate transporter 1Pyrethroids with insecticidal activityChlorinated aromatic avenaciolide analogs with antifungal