CSNpharm
CSNpharm
Teriflunomide, the active metabolite of an approved antirheumatic drug leflunomide, is an emerging oral therapy for multiple sclerosis (MS). It reversibly inhibits dihydroorotate dehydrogenase, the rate-limiting step in the de novo synthesis of pyrimidines.
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CSNpharm
Teriflunomide, the active metabolite of an approved antirheumatic drug leflunomide, is an emerging oral therapy for multiple sclerosis (MS). It reversibly inhibits dihydroorotate dehydrogenase, the rate-limiting step in the de novo synthesis of pyrimidines.
More Information
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CSNpharm
Teriflunomide, the active metabolite of an approved antirheumatic drug leflunomide, is an emerging oral therapy for multiple sclerosis (MS). It reversibly inhibits dihydroorotate dehydrogenase, the rate-limiting step in the de novo synthesis of pyrimidines.
More Information
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CSNpharm
Teriflunomide, the active metabolite of an approved antirheumatic drug leflunomide, is an emerging oral therapy for multiple sclerosis (MS). It reversibly inhibits dihydroorotate dehydrogenase, the rate-limiting step in the de novo synthesis of pyrimidines.
More Information
Supplier Page
CSNpharm
Teriflunomide, the active metabolite of an approved antirheumatic drug leflunomide, is an emerging oral therapy for multiple sclerosis (MS). It reversibly inhibits dihydroorotate dehydrogenase, the rate-limiting step in the de novo synthesis of pyrimidines.
More Information
Supplier Page
CSNpharm
Teriflunomide, the active metabolite of an approved antirheumatic drug leflunomide, is an emerging oral therapy for multiple sclerosis (MS). It reversibly inhibits dihydroorotate dehydrogenase, the rate-limiting step in the de novo synthesis of pyrimidines.
More Information
Supplier Page
CSNpharm
Teriflunomide, the active metabolite of an approved antirheumatic drug leflunomide, is an emerging oral therapy for multiple sclerosis (MS). It reversibly inhibits dihydroorotate dehydrogenase, the rate-limiting step in the de novo synthesis of pyrimidines.
More Information
Supplier Page
CSNpharm
Teriflunomide, the active metabolite of an approved antirheumatic drug leflunomide, is an emerging oral therapy for multiple sclerosis (MS). It reversibly inhibits dihydroorotate dehydrogenase, the rate-limiting step in the de novo synthesis of pyrimidines.
More Information
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CSNpharm
Terpin is an expectorant, commonly used to loosen mucus in patients presenting with acute or chronic bronchitis, and related conditions.
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CSNpharm
Terpin is an expectorant, commonly used to loosen mucus in patients presenting with acute or chronic bronchitis, and related conditions.
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CSNpharm
Terpinen-4-ol, a naturally occurring monoterpene, is the main bioactive component of tea-tree oil and has been shown to have many biological activities such as antifungal properties.
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CSNpharm
CSNpharm
Tert-Butyl 2-(dimethoxyphosphoryl)acetate is reactant for preparation of phosphonate terminated PPH dendrimers as anti-HIV-1 agents and preparation of monodehydro diketopiperazines from ketoacyl amino acid amides via acid-catalyzed cyclization etc.
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CSNpharm
Tetraethylammonium bromide is used as the source of tetraethylammonium ions in pharmacological and physiological studies, but is also used in organic chemical synthesis.
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CSNpharm
Tetraethylammonium chloride is a non-selective potassium channel blocker. Tetraethylammonium chloride is a good substrate for organic cation transporter (OCTN1). Tetraethylammonium chloride antitumor properties[1][2].
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CSNpharm
CSNpharm
Tetrahydroamentoflavone, a potent XO inhibitor isolated and purified from the herbs of Selaginella uncinata, exerts its antioxidant activity in vitro through metal-chelating, and radical-scavenging, and has anti-inflammatory effects. It shows in vitro cyclooxygenase (COX) inhibition activity ( an IC(50) value of 29.5 microM (COX-1) and 40.5% inhibition at 100 mg/mL (COX-2)).
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CSNpharm
Tetrahydroamentoflavone, a potent XO inhibitor isolated and purified from the herbs of Selaginella uncinata, exerts its antioxidant activity in vitro through metal-chelating, and radical-scavenging, and has anti-inflammatory effects. It shows in vitro cyclooxygenase (COX) inhibition activity ( an IC(50) value of 29.5 microM (COX-1) and 40.5% inhibition at 100 mg/mL (COX-2)).
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CSNpharm
Tetrahydrobiopterin is a cofactor of the aromatic amino acid hydroxylases enzymes and also acts as an essential cofactor for all nitric oxide synthase (NOS) isoforms.
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CSNpharm
Tetrahydrobiopterin is a cofactor of the aromatic amino acid hydroxylases enzymes and also acts as an essential cofactor for all nitric oxide synthase (NOS) isoforms.
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CSNpharm
Tetrahydrobiopterin is a cofactor of the aromatic amino acid hydroxylases enzymes and also acts as an essential cofactor for all nitric oxide synthase (NOS) isoforms.
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CSNpharm
Tetrahydrocoptisine is a natural alkaloid compound isolated and purified from Corydalis tubers with anti-inflammatory and anti-parasitic activities.
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CSNpharm
Tetrahydrocoptisine is a natural alkaloid compound isolated and purified from Corydalis tubers with anti-inflammatory and anti-parasitic activities.
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CSNpharm
Tetrahydrocurcumin, a natural product isolated and purified from the rhizomes of Curcuma longa L., is one of the major metabolites of Curcumin. It is an apoptosis inducer and has been demonstrated to be an antioxidant.
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CSNpharm
Tetrahydrocurcumin, a natural product isolated and purified from the rhizomes of Curcuma longa L., is one of the major metabolites of Curcumin. It is an apoptosis inducer and has been demonstrated to be an antioxidant.
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CSNpharm
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CSNpharm
Tetrahydropalmatine is an isoquinoline alkaloid mainly found in the genus Corydalis with analgesic effects. It antagonizes dopamine D1, and D2 receptors as well as actions at dopamine D3, alpha adrenergic and serotonin receptors, with Ki values of 124 nM and 388 nM for D1 and D2 dopamine receptors, respectively.
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CSNpharm
Tetrahydropalmatine is an isoquinoline alkaloid mainly found in the genus Corydalis with analgesic effects. It antagonizes dopamine D1, and D2 receptors as well as actions at dopamine D3, alpha adrenergic and serotonin receptors, with Ki values of 124 nM and 388 nM for D1 and D2 dopamine receptors, respectively.
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Tetrahydrozoline HCl is an imidazole-derived alpha-adrenergic receptor agonist which can result vasoconstriction and decreased nasal and ophthalmic congestion.
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CSNpharm
Tetrahydrozoline HCl is an imidazole-derived alpha-adrenergic receptor agonist which can result vasoconstriction and decreased nasal and ophthalmic congestion.
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CSNpharm
Tetramethylpyrazine, a natural product isolated and purified from the rhizome of Ligusticum chuanxiong Hort., can protect against CoCl2 -induced neurotoxicity and apoptosis in PC12 cells and in rats.
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CSNpharm
Tetramethylpyrazine, a natural product isolated and purified from the rhizome of Ligusticum chuanxiong Hort., can protect against CoCl2 -induced neurotoxicity and apoptosis in PC12 cells and in rats.
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CSNpharm
Tetramethylrhodamine Ethyl Ester Perchlorate is a specific dye for mitochondria with λex and λem of 550 nm, 575 nm, respectively.
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CSNpharm
Tetramethylrhodamine Ethyl Ester Perchlorate is a specific dye for mitochondria with λex and λem of 550 nm, 575 nm, respectively.
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CSNpharm
TMRM Perchlorate is a red fluorescent dye with cell-permeant cationic lipophilic (λex and λem are 530 nm, 592 nm, respectively).
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CSNpharm
TMRM Perchlorate is a red fluorescent dye with cell-permeant cationic lipophilic (λex and λem are 530 nm, 592 nm, respectively).
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CSNpharm
TMRM Perchlorate is a red fluorescent dye with cell-permeant cationic lipophilic (λex and λem are 530 nm, 592 nm, respectively).
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CSNpharm