Bidenoside C is a flavonoid found in brazilian propolis, the first of its kind to be isolated from a herb of the genus Leech, and has anti-proliferative activity against cancer cells.

Bidisomide is an agent of class I antiarrhythmic.

Bidisomide is an agent of class I antiarrhythmic.

Bidisomide is an agent of class I antiarrhythmic.

Bidisomide is an agent of class I antiarrhythmic.

Bidisomide is an agent of class I antiarrhythmic.

Bidisomide is an agent of class I antiarrhythmic.

Bidisomide is an agent of class I antiarrhythmic.

Bidisomide is an agent of class I antiarrhythmic.

Bidwillon A is a useful organic compound for research related to life sciences and the catalog number is T130026.

Biebrich scarlet is a scarlet dye, it has been used in Masson’s trichrome stain for the staining of collagen. It has also been used for the staining of eosinophil.

Biebrich scarlet is a scarlet dye, it has been used in Masson’s trichrome stain for the staining of collagen. It has also been used for the staining of eosinophil.

Bietamiverine(Paparid) is a biochemical spasmodic drug.

Bietamiverine dihydrochloride is a spasmolytic biochemical.

Bietanautine is an antiemetic biochemical.

Bietanautine is an antiemetic biochemical.

Bietaserpine lowered blood pressure and also reduced tumor size in mice.

Bietaserpine lowered blood pressure and also reduced tumor size in mice.

Bietaserpine lowered blood pressure and also reduced tumor size in mice.

Bifemelane is a nootropic compound that causes the first peak by stimulating release from intracellular Ca 2+ stores and the second by capacitive entry via store–operated Ca 2+ channels. Bifemelane will be offered as a pharmacological tool for basic research on astrocytes [1].

Bifemelane is a nootropic compound that causes the first peak by stimulating release from intracellular Ca 2+ stores and the second by capacitive entry via store–operated Ca 2+ channels. Bifemelane will be offered as a pharmacological tool for basic research on astrocytes [1].

Bifemelane is a nootropic compound that causes the first peak by stimulating release from intracellular Ca 2+ stores and the second by capacitive entry via store–operated Ca 2+ channels. Bifemelane will be offered as a pharmacological tool for basic research on astrocytes [1].

Bifemelane hydrochloride is a MAO inhibitor

Bifemelane hydrochloride is a MAO inhibitor

Bifemelane hydrochloride is a MAO inhibitor

Bifemelane hydrochloride is a MAO inhibitor

Bifemelane hydrochloride is a MAO inhibitor

Bifemelane hydrochloride is a MAO inhibitor

Bifemelane hydrochloride is a MAO inhibitor

Bifemelane hydrochloride is a MAO inhibitor

Bifenazate is a positive allosteric modulator of GABA receptor. Bifenazate is an acaricide that controls 100% of mites at a concentration of 25 ppm.

Bifenazate is a positive allosteric modulator of GABA receptor. Bifenazate is an acaricide that controls 100% of mites at a concentration of 25 ppm.

Bifendate (Bifendatatum) is commonly used to treat the transaminase elevation that caused by viral hepatitis and drug-induced liver injury.

Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia.

Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia.

Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia.

Bifeprunox is a partial dopamine and serotonin agonist potentially for the treatment of schizophrenia. Bifeprunox suppresses in vivo VTA dopaminergic neuronal activity via D2 and not D3 dopamine autoreceptor activation. Bifeprunox influences nicotine-seeking behaviour in response to drug-associated stimuli in rats.

Bifeprunox is a partial dopamine and serotonin agonist potentially for the treatment of schizophrenia. Bifeprunox suppresses in vivo VTA dopaminergic neuronal activity via D2 and not D3 dopamine autoreceptor activation. Bifeprunox influences nicotine-seeking behaviour in response to drug-associated stimuli in rats.

Bifeprunox is a partial dopamine and serotonin agonist potentially for the treatment of schizophrenia. Bifeprunox suppresses in vivo VTA dopaminergic neuronal activity via D2 and not D3 dopamine autoreceptor activation. Bifeprunox influences nicotine-seeking behaviour in response to drug-associated stimuli in rats.