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Florfenicol is a fluorinated synthetic amphenicol class of antibiotic, mainly used in veterinary medicine to treat bacterial infections in food-producing animals.
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Florfenicol is a fluorinated synthetic amphenicol class of antibiotic, mainly used in veterinary medicine to treat bacterial infections in food-producing animals.
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Flosequinan is a quinolone vasodilator to treat people with heart failure who could not tolerate ACE inhibitors or digitalis.
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Floxuridine is an oncology drug that belongs to antimetabolites with an GI50 of 5.1 μM for the inhibition of PEPT1.
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Floxuridine is an oncology drug that belongs to antimetabolites with an GI50 of 5.1 μM for the inhibition of PEPT1.
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Fluconazole, an inhibitor of CYP2C19, CYP2C9 and CYP3A4, is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections.
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Fluconazole, an inhibitor of CYP2C19, CYP2C9 and CYP3A4, is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections.
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Fludarabine, a DNA synthesis inhibitor, is a chemotherapy drug used in the treatment of hematological malignancies.
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Fludarabine, a DNA synthesis inhibitor, is a chemotherapy drug used in the treatment of hematological malignancies.
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Fludarabine, a DNA synthesis inhibitor, is a chemotherapy drug used in the treatment of hematological malignancies.
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Fludarabine phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis.
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Fludarabine phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis.
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CSNpharm
Fludarabine phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis.
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Flufenamic Acid is a COX inhibitor and prevents formation of prostaglandins, binds to and reduce the activity of prostaglandin F synthase and activate TRPC6, it is a NSAID drug.
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CSNpharm
Flufenamic Acid is a COX inhibitor and prevents formation of prostaglandins, binds to and reduce the activity of prostaglandin F synthase and activate TRPC6, it is a NSAID drug.
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Flunixin meglumine is a potent inhibitor of COX used as analgesic agent with anti-inflammatory and antipyretic activity.
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CSNpharm
Flunixin meglumine is a potent inhibitor of COX used as analgesic agent with anti-inflammatory and antipyretic activity.
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CSNpharm
Flunixin meglumine is a potent inhibitor of COX used as analgesic agent with anti-inflammatory and antipyretic activity.
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CSNpharm
Fluorescamine is a spiro compound that is not fluorescent itself, but reacts with primary amines to form highly fluorescent products.
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CSNpharm
Fluorescamine is a spiro compound that is not fluorescent itself, but reacts with primary amines to form highly fluorescent products.
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Fluorescein diacetate is a cell-permeant esterase substrate that can serve as a viability probe that measures both enzymatic activity, which is require to activate its fluorescence, and cell-membrane integrity, which is required for intracellular retention of their fluorescent product.
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Fluorescein-5-maleimide is a fluorescent thiol-reactive dye used to conjugate fluorescein to proteins (excitation: 494 nm, emission: 519 nm).
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CSNpharm
Fluorescein-5-maleimide is a fluorescent thiol-reactive dye used to conjugate fluorescein to proteins (excitation: 494 nm, emission: 519 nm).
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CSNpharm
Fluorescein-5-maleimide is a fluorescent thiol-reactive dye used to conjugate fluorescein to proteins (excitation: 494 nm, emission: 519 nm).
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CSNpharm
Fluoroquinolonic acid acts as an intermediate during the synthesis of ciprofloxacin HCl which is a broad-spectrum antibacterial agent.
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CSNpharm
Fluoroquinolonic acid acts as an intermediate during the synthesis of ciprofloxacin HCl which is a broad-spectrum antibacterial agent.
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CSNpharm
Fluoroquinolonic acid acts as an intermediate during the synthesis of ciprofloxacin HCl which is a broad-spectrum antibacterial agent.
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CSNpharm
Fluoroquinolonic acid acts as an intermediate during the synthesis of ciprofloxacin HCl which is a broad-spectrum antibacterial agent.
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CSNpharm
Fluoxetine HCl, an antidepressant, is an inhibitor of the selective serotonin reuptake with Kd of 0.81 nM against serotonin transporter.
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Fluoxetine HCl, an antidepressant, is an inhibitor of the selective serotonin reuptake with Kd of 0.81 nM against serotonin transporter.
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