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

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

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

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

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

(+)-Pinanediol is an effective inducer of melanogenesis. In S91 cells, it acts by inducing higher levels of pigmentation and synthesis of nitric oxide (NO).

(+)-Pinanediol is an effective inducer of melanogenesis. In S91 cells, it acts by inducing higher levels of pigmentation and synthesis of nitric oxide (NO).

(+)-Pinoresinol monomethyl ether 4-O-β-D-glucoside is a natural product.

(+)-S-myricanol shows anti-oxidant and anti-inflammatory activities.

(+)-SHIN1 ((+)-RZ-2994) is an active (+) enantiomer of SHIN1 [1]. SHIN1 is a human serine hydroxymethyltransferse 1 and 2 (SHMT1/2) inhibitor.

(+)-SHIN1 ((+)-RZ-2994) is an active (+) enantiomer of SHIN1 [1]. SHIN1 is a human serine hydroxymethyltransferse 1 and 2 (SHMT1/2) inhibitor.

(+)-SJ733 is an anti-malaria compound. (+)-SJ733 can also inhibit Na+-ATPase PfATP4.

(+)-SJ733 is an anti-malaria compound. (+)-SJ733 can also inhibit Na+-ATPase PfATP4.

(+)-SJ733 is an anti-malaria compound. (+)-SJ733 can also inhibit Na+-ATPase PfATP4.

(+)-SJ733 is an anti-malaria compound. (+)-SJ733 can also inhibit Na+-ATPase PfATP4.

(+)-SJ733 is an anti-malaria compound. (+)-SJ733 can also inhibit Na+-ATPase PfATP4.

(+)-SJ733 is an anti-malaria compound. (+)-SJ733 can also inhibit Na+-ATPase PfATP4.

(+)-Sotalol ((S)-Sotalol) is the S-isomer of Sotalol . Sotalol is an orally active, non-selective β-adrenergic receptor blocker. (+)-Sotalol is an antiarrhythmic agent. (+)-Sotalol can prolong action potential duration in isolated cardiac muscle [1] [2] [3] .

(+)-Sotalol ((S)-Sotalol) is the S-isomer of Sotalol . Sotalol is an orally active, non-selective β-adrenergic receptor blocker. (+)-Sotalol is an antiarrhythmic agent. (+)-Sotalol can prolong action potential duration in isolated cardiac muscle [1] [2] [3] .

(+)-Sotalol ((S)-Sotalol) is the S-isomer of Sotalol . Sotalol is an orally active, non-selective β-adrenergic receptor blocker. (+)-Sotalol is an antiarrhythmic agent. (+)-Sotalol can prolong action potential duration in isolated cardiac muscle [1] [2] [3] .

Pachycarpine is a natural product extracted from scotch broom, is a sodium channel blocker and a class 1a antiarrhythmic agent

(+)-Syringaresinol shows antioxidant potential, it exhibits cytoprotective activity in cultured MCF-7 cells stressed by H2O2.

(+)-Syringaresinol shows antioxidant potential, it exhibits cytoprotective activity in cultured MCF-7 cells stressed by H2O2.

(+)-Tetrabenazine is a reversible vesicular monoamine transporter 2 (VMAT-2) inhibitor, inhibits transport by VMAT2 with 10-fold greater potency than transport by VMAT1.

(+)-Tetrabenazine is a reversible vesicular monoamine transporter 2 (VMAT-2) inhibitor, inhibits transport by VMAT2 with 10-fold greater potency than transport by VMAT1.

(+)-Tetrabenazine is a reversible vesicular monoamine transporter 2 (VMAT-2) inhibitor, inhibits transport by VMAT2 with 10-fold greater potency than transport by VMAT1.

(+)-Tetrabenazine is a reversible vesicular monoamine transporter 2 (VMAT-2) inhibitor, inhibits transport by VMAT2 with 10-fold greater potency than transport by VMAT1.

(+)-Tetrabenazine is a reversible vesicular monoamine transporter 2 (VMAT-2) inhibitor, inhibits transport by VMAT2 with 10-fold greater potency than transport by VMAT1.

(+)-Tetrabenazine is a reversible vesicular monoamine transporter 2 (VMAT-2) inhibitor, inhibits transport by VMAT2 with 10-fold greater potency than transport by VMAT1.

(+)-Tomoxetine hydrochloride is a bioactive chemical.

(+)-Tomoxetine hydrochloride is a bioactive chemical.

(+)-trans-Isolimonene is a natural product (monoterpene) isolated from essential oil.

(+)-trans-Isolimonene is a natural product (monoterpene) isolated from essential oil.

(+)-U-50488 ((+)-Trans-(1R,2R)-U-50488) is a less active κ opioid receptor (KOR) agonist than the enantiomer of (-)-Trans-(1S,2S)-U-50488 [1] .

(+)-U-50488 ((+)-Trans-(1R,2R)-U-50488) is a less active κ opioid receptor (KOR) agonist than the enantiomer of (-)-Trans-(1S,2S)-U-50488 [1] .

D2 antagonist

D2 antagonist

D2 antagonist

(+)-Usnic acid (D-Usnic Acid) is a naturally occurring dibenzofuran derivative found in several lichen species.

(+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.