ligands acting on targets

(+)-nootkatone, a bicyclic conjugated sesquiterpene ketone with a grapefruit-like flavor, is commonly used in fragrance, food, cosmetics and pharmaceutical industry. It can be synthesized from (+)-valencene via biotransformation. (+)-nootkatone is

(+)-nootkatone, a bicyclic conjugated sesquiterpene ketone with a grapefruit-like flavor, is commonly used in fragrance, food, cosmetics and pharmaceutical industry. It can be synthesized from (+)-valencene via biotransformation. (+)-nootkatone is

(+)-norfenfluramine.

(+)-norfenfluramine.

(&amp:plus:)-Norfenfluramine is the major hepatic metabolite of (&amp:plus:)-fenfluramine and is primarily responsible for the anorexic effect, as well as side effects: (&amp:plus:)-norfenfluramine causes vasoconstriction and a blood pressure

(&amp:plus:)-Norfenfluramine is the major hepatic metabolite of (&amp:plus:)-fenfluramine and is primarily responsible for the anorexic effect, as well as side effects: (&amp:plus:)-norfenfluramine causes vasoconstriction and a blood pressure

(&amp:plus:)-Norfenfluramine is the major hepatic metabolite of (&amp:plus:)-fenfluramine and is primarily responsible for the anorexic effect, as well as side effects: (&amp:plus:)-norfenfluramine causes vasoconstriction and a blood pressure

(&amp:plus:)-Norfenfluramine is the major hepatic metabolite of (&amp:plus:)-fenfluramine and is primarily responsible for the anorexic effect, as well as side effects: (&amp:plus:)-norfenfluramine causes vasoconstriction and a blood pressure

(+)-Oxypeucedanin methanolate (compound 9) is a natural compound with inhibitory effect on prostaglandin E2 production.

(+)-Oxypeucedanin methanolate (compound 9) is a natural compound with inhibitory effect on prostaglandin E2 production.

(+)-PD 128907 hydrochloride is a selective dopamine D2/D3 receptor agonist, with Kis of 1.7, 0.84 nM for human and rat D3 receptors, 179, 770 n M for human and rat D3 receptors, respectively.

(+)-PD 128907 hydrochloride is a selective dopamine D2/D3 receptor agonist, with Kis of 1.7, 0.84 nM for human and rat D3 receptors, 179, 770 n M for human and rat D3 receptors, respectively.