CSNpharm
Tiadinil is a plant activator of systemic acquired resistance, boosts the production of herbivore-induced plant volatiles and is an insecticide agent.
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CSNpharm
Tiadinil is a plant activator of systemic acquired resistance, boosts the production of herbivore-induced plant volatiles and is an insecticide agent.
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CSNpharm
Tiadinil is a plant activator of systemic acquired resistance, boosts the production of herbivore-induced plant volatiles and is an insecticide agent.
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CSNpharm
Tiagabine HCl is an inhibitor of gamma-aminobutyric acid (GABA) reuptake (IC50 = 67 nM in vivo) with anticonvulsant effect.
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CSNpharm
Tiagabine HCl is an inhibitor of gamma-aminobutyric acid (GABA) reuptake (IC50 = 67 nM in vivo) with anticonvulsant effect.
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CSNpharm
Tiagabine HCl is an inhibitor of gamma-aminobutyric acid (GABA) reuptake (IC50 = 67 nM in vivo) with anticonvulsant effect.
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CSNpharm
Thioridazine is an antipsychotic drug, used in the treatment of schizophrenia and psychosis, shows D4 selectivity or serotonin antagonism.
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TIC10 isomer is an isomer of TIC10, a potent, orally active, and stable small molecule that transcriptionally induces TRAIL in a p53-independent manner and crosses the blood-brain barrier.
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CSNpharm
TIC10 isomer is an isomer of TIC10, a potent, orally active, and stable small molecule that transcriptionally induces TRAIL in a p53-independent manner and crosses the blood-brain barrier.
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CSNpharm
TIC10 isomer is an isomer of TIC10, a potent, orally active, and stable small molecule that transcriptionally induces TRAIL in a p53-independent manner and crosses the blood-brain barrier.
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CSNpharm
TIC10 isomer is an isomer of TIC10, a potent, orally active, and stable small molecule that transcriptionally induces TRAIL in a p53-independent manner and crosses the blood-brain barrier.
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CSNpharm
TIC10 isomer is an isomer of TIC10, a potent, orally active, and stable small molecule that transcriptionally induces TRAIL in a p53-independent manner and crosses the blood-brain barrier.
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CSNpharm
TIC10 isomer is an isomer of TIC10, a potent, orally active, and stable small molecule that transcriptionally induces TRAIL in a p53-independent manner and crosses the blood-brain barrier.
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CSNpharm
Ticagrelor is a reversibly and oral active P2Y12 receptor antagonist with Ki of 2 nM, also inhibits CYP2C9 and midazolam 4-hydroxylation with IC50 of 10.5 μM and 8.2 μM respectively.
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CSNpharm
Ticagrelor is a reversibly and oral active P2Y12 receptor antagonist with Ki of 2 nM, also inhibits CYP2C9 and midazolam 4-hydroxylation with IC50 of 10.5 μM and 8.2 μM respectively.
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CSNpharm
Ticagrelor is a reversibly and oral active P2Y12 receptor antagonist with Ki of 2 nM, also inhibits CYP2C9 and midazolam 4-hydroxylation with IC50 of 10.5 μM and 8.2 μM respectively.
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CSNpharm
Ticarcillin is a semisynthetic antibiotic with a broad spectrum of bactericidal activity against many Gram-positive and Gram-negative aerobic and anaerobic bacteria.
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Ticlopidine is an antiplatelet drug in the thienopyridine family which is an adenosine diphosphate (ADP) receptor inhibitor.
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CSNpharm
Ticlopidine is an antiplatelet drug in the thienopyridine family which is an adenosine diphosphate (ADP) receptor inhibitor.
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CSNpharm
Ticlopidine is an antiplatelet drug in the thienopyridine family which is an adenosine diphosphate (ADP) receptor inhibitor.
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CSNpharm
Ticlopidine is an antiplatelet drug in the thienopyridine family which is an adenosine diphosphate (ADP) receptor inhibitor.
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CSNpharm
Ticlopidine HCl is an adenosine diphosphate (ADP) receptor inhibitor that against platelet aggregation with IC50 of ~2 μM.
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CSNpharm
Ticlopidine HCl is an adenosine diphosphate (ADP) receptor inhibitor that against platelet aggregation with IC50 of ~2 μM.
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CSNpharm
Tie2 kinase inhibitor is an optimized compound of SB-203580, selective to Tie2 with IC50 of 0.25 μM, 200-fold more potent than p38.
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CSNpharm
Tie2 kinase inhibitor is an optimized compound of SB-203580, selective to Tie2 with IC50 of 0.25 μM, 200-fold more potent than p38.
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CSNpharm
Tie2 kinase inhibitor is an optimized compound of SB-203580, selective to Tie2 with IC50 of 0.25 μM, 200-fold more potent than p38.
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Tildipirosin is a 16-membered macrolide for treatment, control, and prevention of bovine respiratory disease by inhibiting protein synthesis on the ribosome (IC50= 0.23 ± 0.01 μM).
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CSNpharm
Tildipirosin is a 16-membered macrolide for treatment, control, and prevention of bovine respiratory disease by inhibiting protein synthesis on the ribosome (IC50= 0.23 ± 0.01 μM).
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CSNpharm
Tildipirosin is a 16-membered macrolide for treatment, control, and prevention of bovine respiratory disease by inhibiting protein synthesis on the ribosome (IC50= 0.23 ± 0.01 μM).
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