(-)-Lunacridine is a bioactive chemical.

(-)-Lyoniresinol has antioxidant activity.

(-)-Lyoniresinol has antioxidant activity.

(-)-Lyoniresinol 9′-O-glucoside is a natural product from Phyllostachys heterocycla MITF.

(-) -Mdo-NPA HCl is an oral effective long-acting drug that is active against central dopamine receptors and the similar apophin.

(-) -Mdo-NPA HCl is an oral effective long-acting drug that is active against central dopamine receptors and the similar apophin.

(-) -Mdo-NPA HCl is an oral effective long-acting drug that is active against central dopamine receptors and the similar apophin.

(-)-Menthol (Levomenthol) is a levo isomer of menthol, an organic compound made synthetically or obtained from peppermint or mint oils with flavoring and local anesthetic properties. When added to pharmaceuticals and foods, menthol functions as a fortifier for peppermint flavors. It also has a counterirritant effect on skin and mucous membranes, thereby producing a local […]

(-)-Menthol (Levomenthol) is a levo isomer of menthol, an organic compound made synthetically or obtained from peppermint or mint oils with flavoring and local anesthetic properties. When added to pharmaceuticals and foods, menthol functions as a fortifier for peppermint flavors. It also has a counterirritant effect on skin and mucous membranes, thereby producing a local […]

(-)-Menthone is a natural product.

(-)-Menthone is a natural product.

Mesembrine is a serotonin reuptake inhibitor and is also a weak inhibitor of the enzyme phosphodiesterase 4 (PDE4).

Mesembrine is a serotonin reuptake inhibitor and is also a weak inhibitor of the enzyme phosphodiesterase 4 (PDE4).

Mesembrine is a serotonin reuptake inhibitor and is also a weak inhibitor of the enzyme phosphodiesterase 4 (PDE4).

(-)-Mycousnine is a microbial metabolite and derivative of usnic acid originally isolated fromM. nawaethat has antibacterial and antifungal activities.1,2It is active against the Gram-positive bacteriaB. subtilis,K. rhizophila, andS. aureus(MICs = 4, 8, and 4 g/ml, respectively) but not the Gram-negative bacteriaE. coli,S. typhimurium, andK. pneumoniae(MICs = >128 g/ml for all).2(-)-Mycousnine is also active against the […]

(-)-Mycousnine is a microbial metabolite and derivative of usnic acid originally isolated fromM. nawaethat has antibacterial and antifungal activities.1,2It is active against the Gram-positive bacteriaB. subtilis,K. rhizophila, andS. aureus(MICs = 4, 8, and 4 g/ml, respectively) but not the Gram-negative bacteriaE. coli,S. typhimurium, andK. pneumoniae(MICs = >128 g/ml for all).2(-)-Mycousnine is also active against the […]

N-Methylcoclaurine shows binding affinities for the ĸ opioid receptor with the equilibrium dissociation constant (Ki) value of 0.9 ± 0.1 uM. N-methylcoclaurine also shows promising butyrylcholinesterase inhibition activities, with the IC50 value of 15.0 ± 1.4 uM.

(-)-N-Methylsedridine is a natural product of Sedum, Crassulaceae. The catalog number is TN4615 and the CAS number is 41447-15-8. (-)-N-Methylsedridine can be used as a reference standard.

(S)-2-(1-(2-chloro-4-(pyrrolidin-1-yl)benzoyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl)-N-isopropylacetamide is an antidiuretic hormone V2 receptor agonist used in the treatment of nocturia and urinary incontinence.

(S)-2-(1-(2-chloro-4-(pyrrolidin-1-yl)benzoyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl)-N-isopropylacetamide is an antidiuretic hormone V2 receptor agonist used in the treatment of nocturia and urinary incontinence.

(S)-2-(1-(2-chloro-4-(pyrrolidin-1-yl)benzoyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl)-N-isopropylacetamide is an antidiuretic hormone V2 receptor agonist used in the treatment of nocturia and urinary incontinence.

(S)-2-(1-(2-chloro-4-(pyrrolidin-1-yl)benzoyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl)-N-isopropylacetamide is an antidiuretic hormone V2 receptor agonist used in the treatment of nocturia and urinary incontinence.

(S)-2-(1-(2-chloro-4-(pyrrolidin-1-yl)benzoyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl)-N-isopropylacetamide is an antidiuretic hormone V2 receptor agonist used in the treatment of nocturia and urinary incontinence.

(S)-2-(1-(2-chloro-4-(pyrrolidin-1-yl)benzoyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl)-N-isopropylacetamide is an antidiuretic hormone V2 receptor agonist used in the treatment of nocturia and urinary incontinence.

(S)-2-(1-(2-chloro-4-(pyrrolidin-1-yl)benzoyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl)-N-isopropylacetamide is an antidiuretic hormone V2 receptor agonist used in the treatment of nocturia and urinary incontinence.

(-)-Oxypeucedanin hydrate is a furanocoumarin. It has a role as a metabolite.

(-)-Oxypeucedanin hydrate is a furanocoumarin. It has a role as a metabolite.

(-)-Oxypeucedanin hydrate is a furanocoumarin. It has a role as a metabolite.

(-)-Oxypeucedanin hydrate is a furanocoumarin. It has a role as a metabolite.

(-)-Oxypeucedanin hydrate is a furanocoumarin. It has a role as a metabolite.

(-)-Oxypeucedanin hydrate is a furanocoumarin. It has a role as a metabolite.

p-Bromotetramisole Oxalate is a potent and non-specific inhibitor of alkaline phosphatase.

p-Bromotetramisole Oxalate is a potent and non-specific inhibitor of alkaline phosphatase.

p-Bromotetramisole Oxalate is a potent and non-specific inhibitor of alkaline phosphatase.

p-Bromotetramisole Oxalate is a potent and non-specific inhibitor of alkaline phosphatase.

p-Bromotetramisole Oxalate is a potent and non-specific inhibitor of alkaline phosphatase.

p-Bromotetramisole Oxalate is a potent and non-specific inhibitor of alkaline phosphatase.

p-Bromotetramisole Oxalate is a potent and non-specific inhibitor of alkaline phosphatase.

(-)-Perillaldehyde shows antibacterial activity.

(-)-Perillaldehyde shows antibacterial activity.

(-)-Phaselic acid is a natural product for research related to life sciences. The catalog number is TN5840 and the CAS number is 423170-79-0.

(-)-Phyllocladene is a natural product from Callicarpa macrophylla.

(-)-Phyllocladene is a natural product from Callicarpa macrophylla.

(-)-Pinocembrin exhibits anti-mycobacterium activity against mycobacteriuum tuberculosis H37Ra with an IC 50 value of 1.11 mg/mL in dormant phase and 1.21 mg/mL in active phase, respectively. (-)-Pinocembrin has potent antiproliferative activity with IC 50 values of 1.88-11.00 mg/mL against THP-1, A549, Panc-1, HeLa and MCF7 cell lines .

(-)-Pinocembrin exhibits anti-mycobacterium activity against mycobacteriuum tuberculosis H37Ra with an IC 50 value of 1.11 mg/mL in dormant phase and 1.21 mg/mL in active phase, respectively. (-)-Pinocembrin has potent antiproliferative activity with IC 50 values of 1.88-11.00 mg/mL against THP-1, A549, Panc-1, HeLa and MCF7 cell lines .