Prolintane hydrochloride

Application (1 S ,2 S ,3 R ,5 S )-(+)-Pinanediol can be used as a chiral reagent in the synthesis of homochiral &#945-hydroxyketones and in the resolution of prolineboronate esters.

Application (1 S ,2 S ,3 R ,5 S )-(+)-Pinanediol can be used as a chiral reagent in the synthesis of homochiral &#945-hydroxyketones and in the resolution of prolineboronate esters.

Application (1 S ,2 S ,3 R ,5 S )-(+)-Pinanediol can be used as a chiral reagent in the synthesis of homochiral &#945-hydroxyketones and in the resolution of prolineboronate esters.

Application (1 S ,2 S ,3 R ,5 S )-(+)-Pinanediol can be used as a chiral reagent in the synthesis of homochiral &#945-hydroxyketones and in the resolution of prolineboronate esters.

Application 1,2-Naphthoquinone-4-sulfonic acid sodium salt (Folin&#8242s reagent) was used in the colorimetric assay for determination of procaine hydrochloride in pharmaceutical preparations .

11&beta-PGE2 is the C-11 epimer of PGE2. It is a moderate inhibitor of PGE2 binding to rat hypothalamic membranes with a Ki value of 53 nM.

15-deoxy-Δ|12,14|-Prostaglandin J|2|is one of the cyclopentenone PGs, which have documented metabolic (peroxisome proliferator-activated receptor γ-activating), antimitotic, and antiproliferative effects.(1,2,3) The activity of the compounds in this

15-deoxy-Δ|12,14|-Prostaglandin J|2|is one of the cyclopentenone PGs, which have documented metabolic (peroxisome proliferator-activated receptor γ-activating), antimitotic, and antiproliferative effects.(1,2,3) The activity of the compounds in this

17-phenyl trinor PGD2 is a novel, chemically stable analog of PGD2 wherein the lower side chain is modified by the addition of a phenyl group at C-17 in place of the last 3 &omega-chain carbon atoms. This modification has not been reported in a

17-phenyl trinor PGD2 is a novel, chemically stable analog of PGD2 wherein the lower side chain is modified by the addition of a phenyl group at C-17 in place of the last 3 &omega-chain carbon atoms. This modification has not been reported in a

17-phenyl trinor PGD2 is a novel, chemically stable analog of PGD2 wherein the lower side chain is modified by the addition of a phenyl group at C-17 in place of the last 3 &omega-chain carbon atoms. This modification has not been reported in a

17-phenyl trinor-13,14-dihydro Prostaglandin A|2|is a synthetic PG analog with biological activity not widely reported. The PGF2α analog latanoprost, bearing the same features as the lower side chain, has recently been approved as a pharmaceutical