(-)-Anonaine can be extracted from several species of Magnoliaceae and Annelidae and has antimalarial, antibacterial, antifungal, antioxidant, anticancer, antidepressant and vasodilatory activities. (-)-Anonaine induces apoptosis in human cervical cancer (HeLa) cells, induces DNA damage and inhibits the growth and migration of human lung cancer h1299 cells through Bax and caspase-dependent pathways.

(-)-Anonaine can be extracted from several species of Magnoliaceae and Annelidae and has antimalarial, antibacterial, antifungal, antioxidant, anticancer, antidepressant and vasodilatory activities. (-)-Anonaine induces apoptosis in human cervical cancer (HeLa) cells, induces DNA damage and inhibits the growth and migration of human lung cancer h1299 cells through Bax and caspase-dependent pathways.

(-)-Anonaine can be extracted from several species of Magnoliaceae and Annelidae and has antimalarial, antibacterial, antifungal, antioxidant, anticancer, antidepressant and vasodilatory activities. (-)-Anonaine induces apoptosis in human cervical cancer (HeLa) cells, induces DNA damage and inhibits the growth and migration of human lung cancer h1299 cells through Bax and caspase-dependent pathways.

(-)-Anonaine can be extracted from several species of Magnoliaceae and Annelidae and has antimalarial, antibacterial, antifungal, antioxidant, anticancer, antidepressant and vasodilatory activities. (-)-Anonaine induces apoptosis in human cervical cancer (HeLa) cells, induces DNA damage and inhibits the growth and migration of human lung cancer h1299 cells through Bax and caspase-dependent pathways.

(-)-Asarinin (Eleutheroside B4) shows antibacterial activity.

(-)-Asarinin (Eleutheroside B4) shows antibacterial activity.

D-Aspartic acid (D-Asp) is an endogenous amino acid existing in invertebrates and vertebrates. It can regulate testosterone synthesis and is an agonist of NMDA receptor.

(-)-Benzotetramisole makes an efficient and selective catalyst. (-)-Benzotetramisole is a benzannulated derivative of the anthelmintic compound tetraimidazole 3 and is itself an effective catalyst for conversion.

(-)-Benzotetramisole makes an efficient and selective catalyst. (-)-Benzotetramisole is a benzannulated derivative of the anthelmintic compound tetraimidazole 3 and is itself an effective catalyst for conversion.

(-)-Benzotetramisole makes an efficient and selective catalyst. (-)-Benzotetramisole is a benzannulated derivative of the anthelmintic compound tetraimidazole 3 and is itself an effective catalyst for conversion.

(-)-Benzotetramisole makes an efficient and selective catalyst. (-)-Benzotetramisole is a benzannulated derivative of the anthelmintic compound tetraimidazole 3 and is itself an effective catalyst for conversion.

(-)-Benzotetramisole makes an efficient and selective catalyst. (-)-Benzotetramisole is a benzannulated derivative of the anthelmintic compound tetraimidazole 3 and is itself an effective catalyst for conversion.

(-)-Benzotetramisole makes an efficient and selective catalyst. (-)-Benzotetramisole is a benzannulated derivative of the anthelmintic compound tetraimidazole 3 and is itself an effective catalyst for conversion.

(-)-Benzotetramisole makes an efficient and selective catalyst. (-)-Benzotetramisole is a benzannulated derivative of the anthelmintic compound tetraimidazole 3 and is itself an effective catalyst for conversion.

(-)-Bicuculline methobromide is a potent antagonist of GABAA receptor .

(-)-Bicuculline methochloride is a potent antagonist of GABAA receptor.

(-)-Bicuculline methochloride is a potent antagonist of GABAA receptor.

(-)-Bicuculline methochloride is a potent antagonist of GABAA receptor.

(-)-Blebbistatin is an S enantiomer of blebbistatin. It is a potent and selective myosin II inhibitor with IC50 ranging from 0.5 to 5 μM.

(-)-Blebbistatin is an S enantiomer of blebbistatin. It is a potent and selective myosin II inhibitor with IC50 ranging from 0.5 to 5 μM.

(-)-Borneol has a highly efficacious positive modulating action at GABA receptor with an EC50 of 237 μM.

(-)-Borneol has a highly efficacious positive modulating action at GABA receptor with an EC50 of 237 μM.

(-)-Bornyl acetate is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate isolates from hyssop oil and possesses antifungal activity. (-)-Bornyl acetate shows highly active whitening and antioxidant activities, has potential applications in cosmeceutical materials. (-)-Bornyl acetate downregulated the levels of proinflammatory cytokines in vitro and in vivo; reduced the number of total cells, neutrophils, […]

(-)-Bornyl acetate is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate isolates from hyssop oil and possesses antifungal activity. (-)-Bornyl acetate shows highly active whitening and antioxidant activities, has potential applications in cosmeceutical materials. (-)-Bornyl acetate downregulated the levels of proinflammatory cytokines in vitro and in vivo; reduced the number of total cells, neutrophils, […]

(-)-Bornyl acetate is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate isolates from hyssop oil and possesses antifungal activity. (-)-Bornyl acetate shows highly active whitening and antioxidant activities, has potential applications in cosmeceutical materials. (-)-Bornyl acetate downregulated the levels of proinflammatory cytokines in vitro and in vivo; reduced the number of total cells, neutrophils, […]

(-)-Butin has antioxidant activity, can protect cells against H2O2-induced apoptosis, oxidative DNA damage and oxidative mitochondrial dysfunction; it attenuates oxidative stress by activating Nrf2-mediated Mn SOD induction via the PI3K/Akt signaling pathway.

(-)-Butin has antioxidant activity, can protect cells against H2O2-induced apoptosis, oxidative DNA damage and oxidative mitochondrial dysfunction; it attenuates oxidative stress by activating Nrf2-mediated Mn SOD induction via the PI3K/Akt signaling pathway.

(-)-Butin has antioxidant activity, can protect cells against H2O2-induced apoptosis, oxidative DNA damage and oxidative mitochondrial dysfunction; it attenuates oxidative stress by activating Nrf2-mediated Mn SOD induction via the PI3K/Akt signaling pathway.

(-)-Butin has antioxidant activity, can protect cells against H2O2-induced apoptosis, oxidative DNA damage and oxidative mitochondrial dysfunction; it attenuates oxidative stress by activating Nrf2-mediated Mn SOD induction via the PI3K/Akt signaling pathway.

(1S,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one also known by its common name as (-)-Camphor is a chiral intermediate of camphor and is used as a flavour additive in foods and sweetners.

(1S,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one also known by its common name as (-)-Camphor is a chiral intermediate of camphor and is used as a flavour additive in foods and sweetners.

(-)-Camphoric acid is a less active enantiomer of Camphoric acid which induces GluR expression.

(-)-Camphoric acid is a less active enantiomer of Camphoric acid which induces GluR expression.

(-)-Carvone is a natural product which probably has antioxidant and anti-inflammatory capabilities.

(-)-Carvone is a natural product which probably has antioxidant and anti-inflammatory capabilities.

(-)-Catechin, an isomer of catechin, inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM.

(-)-Catechin, an isomer of catechin, inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM.

(-)-Catechin, an isomer of catechin, inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM.

(-)-Catechin, an isomer of catechin, inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM.

(-)-Catechin, an isomer of catechin, inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM.