(+)-Norfenfluramine hydrochloride, a major hepatic metabolite of (+)-fenfluramine, is a selective 5-HT 2B receptor agonist ( K i : 11.2 nM). (+)-Norfenfluramine hydrochloride potently stimulates the hydrolysis of inositol phosphates and increases intracellular Ca 2+ . (+)-Norfenfluramine hydrochloride can be used for the research of primary pulmonary hypertension and valvular heart disease .

(+)-Norgestrel is a progestin medication for the treatment of birth control pills and in menopausal hormone therapy.

(+)-Norgestrel is a progestin medication for the treatment of birth control pills and in menopausal hormone therapy.

(+)-Norgestrel is a progestin medication for the treatment of birth control pills and in menopausal hormone therapy.

(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity.

(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity.

(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity.

(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity.

(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity.

(+)-ORM-10921 is a conformation of ORM-10921 and can be used in chemical synthesis studies.

(+)-ORM-10921 is a conformation of ORM-10921 and can be used in chemical synthesis studies.

(+)-ORM-10921 is a conformation of ORM-10921 and can be used in chemical synthesis studies.

(+)-ORM-10921 is a conformation of ORM-10921 and can be used in chemical synthesis studies.

(+)-ORM-10921 is a conformation of ORM-10921 and can be used in chemical synthesis studies.

(+)-ORM-10921 is a conformation of ORM-10921 and can be used in chemical synthesis studies.

(+)-OSU 6162 is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

(+)-OSU 6162 is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

(+)-OSU 6162 is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

(+)-OSU 6162 is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

(+)-OSU 6162 is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

(+)-OSU 6162 is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

(+)-OSU 6162 is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

(+)-OSU 6162 is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

(+)-PD 128907 hydrochloride is an agonist of D3 dopamine receptor .

(+)-PD 128907 hydrochloride is an agonist of D3 dopamine receptor .

(+)-PD 128907 hydrochloride is an agonist of D3 dopamine receptor .

(+)-PD 128907 hydrochloride is an agonist of D3 dopamine receptor .

(+)-PD 128907 hydrochloride is an agonist of D3 dopamine receptor .

(+)-PD 128907 hydrochloride is an agonist of D3 dopamine receptor .

(+)-Penbutolol is an antagonist of β-adrenoceptor(IC50 of 0.74 μM). (+)-Penbutolol is an optical isomer of l-penbutolol with Na+ channel-blocking action.

(+)-Penbutolol is an antagonist of β-adrenoceptor(IC50 of 0.74 μM). (+)-Penbutolol is an optical isomer of l-penbutolol with Na+ channel-blocking action.

(+)-Perillaldehyde is a natural product.

(+)-Peusedanol is a natural product isolated from Peucedanumjaponicum.

(+)-Peusedanol is a natural product isolated from Peucedanumjaponicum.

(+)-Peusedanol is a natural product isolated from Peucedanumjaponicum.

(+)-Peusedanol is a natural product isolated from Peucedanumjaponicum.

(+)-Peusedanol is a natural product isolated from Peucedanumjaponicum.

(+)-Peusedanol is a natural product isolated from Peucedanumjaponicum.

(+)-Phenserine is a novel selective inhibitor of cholinesterase non-competitive (IC50: 45.3 μM).

(+)-Phenserine is a novel selective inhibitor of cholinesterase non-competitive (IC50: 45.3 μM).

(+)-Phenserine is a novel selective inhibitor of cholinesterase non-competitive (IC50: 45.3 μM).

(+)-Picumeterol is a mixture of all configurations of Picumeterol.

(+)-Picumeterol is a mixture of all configurations of Picumeterol.