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Showing 251 to 253 of 20 results

Product	Utech#	UOM	Mfg#	Price
Nsaid And Cox-2 Inhibitor Used To Treat Pain And Inflammation. It Also Induces Apoptosis In Hepatoma Cells And Indirectly Activates Sirt1, Each	5583465	EA	C1644-100 mg	$ 206.48
Cytochrome C Binding Agent That Inhibits Electron Transport Chain Activity, Oxidative Phosphorylation, And Atp Synthesis, Each	5583496	EA	A5378-10 mg	$ 323.92
Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each	5583507	EA	C2844-50 g	$ 337.49
Nsaid And Cox-2 Inhibitor Used To Treat Pain And Inflammation. It Also Induces Apoptosis In Hepatoma Cells And Indirectly Activates Sirt1, Each	5583526	EA	C1644-500 mg	$ 430.57
Nsaid And Cox-2 Inhibitor Used To Treat Pain And Inflammation. It Also Induces Apoptosis In Hepatoma Cells And Indirectly Activates Sirt1, Each	5583565	EA	C1644-1 g	$ 662.06
Cytochrome C Binding Agent That Inhibits Electron Transport Chain Activity, Oxidative Phosphorylation, And Atp Synthesis, Each	5583596	EA	A5378-50 mg	$ 772.22
Rig1-Like Receptor Antagonist Found In Andrographis. It Decreases Tnf-A-Induced Generation Of Ros, Suppresses Development Of Diabetes, And Inhibits Hsp90 Activity And Induces Apoptosis In Leukemia Cells, Each	5583635	EA	A5313-10 mg	$ 65.58
Endogenous Clr-Ramp2/3 Receptor Agonist Involved In Cell Growth And Differentiation. It Decreases Blood Pressure, Increases Neovascularization, And Binds Microtubule-Associated Proteins In The Cytoskeleton, Each	5583698	EA	A1607-25 mg	$ 113.86
Rig1-Like Receptor Antagonist Found In Andrographis. It Decreases Tnf-A-Induced Generation Of Ros, Suppresses Development Of Diabetes, And Inhibits Hsp90 Activity And Induces Apoptosis In Leukemia Cells, Each	5583709	EA	A5313-100 mg	$ 121.92
Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each	5583720	EA	C2845-5 g	$ 86.18
Prodrug Of 5-Fu And Inhibitor Of Thymidylate Synthase That Is Used To Treat Various Cancers. It Inhibits Dna Synthesis, Each	5583867	EA	C0162-250 mg	$ 176.85
Pp1/2A Inhibitor Found In Canarthis Vesicatoria. It Inhibits Proliferation Of Colorectal Cancer Cells, Increases Mcp-1, Il-6, And Il-1Ss Levels, And Inhibits Differentiation And Resorptive Activity Of Osteoclasts, Each	5583878	EA	C0255-25 mg	$ 183.44
Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each	5583918	EA	C2845-10 g	$ 124.41
Rig1-Like Receptor Antagonist Found In Andrographis. It Decreases Tnf-A-Induced Generation Of Ros, Suppresses Development Of Diabetes, And Inhibits Hsp90 Activity And Induces Apoptosis In Leukemia Cells, Each	5583961	EA	A5313-250 mg	$ 222.96
Endogenous Clr-Ramp2/3 Receptor Agonist Involved In Cell Growth And Differentiation. It Decreases Blood Pressure, Increases Neovascularization, And Binds Microtubule-Associated Proteins In The Cytoskeleton, Each	5584095	EA	A1607-100 mg	$ 326.80
Aromatase Inhibitor Used To Treat Er-Positive Breast Cancer. It Suppresses Estrogen Synthesis And Induces Apoptosis In Breast Cancer Cells, Each	5584140	EA	A5302-100 mg	$ 332.26
Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each	5584325	EA	C2845-50 g	$ 239.15
Prodrug Of 5-Fu And Inhibitor Of Thymidylate Synthase That Is Used To Treat Various Cancers. It Inhibits Dna Synthesis, Each	5584353	EA	C0162-1 g	$ 531.11
Pp1/2A Inhibitor Found In Canarthis Vesicatoria. It Inhibits Proliferation Of Colorectal Cancer Cells, Increases Mcp-1, Il-6, And Il-1Ss Levels, And Inhibits Differentiation And Resorptive Activity Of Osteoclasts, Each	5584358	EA	C0255-100 mg	$ 537.67
Aromatase Inhibitor Used To Treat Er-Positive Breast Cancer. It Suppresses Estrogen Synthesis And Induces Apoptosis In Breast Cancer Cells, Each	5584428	EA	A5302-250 mg	$ 611.07

Nsaid And Cox-2 Inhibitor Used To Treat Pain And Inflammation. It Also Induces Apoptosis In Hepatoma Cells And Indirectly Activates Sirt1, Each

Cytochrome C Binding Agent That Inhibits Electron Transport Chain Activity, Oxidative Phosphorylation, And Atp Synthesis, Each

Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each

Nsaid And Cox-2 Inhibitor Used To Treat Pain And Inflammation. It Also Induces Apoptosis In Hepatoma Cells And Indirectly Activates Sirt1, Each

Nsaid And Cox-2 Inhibitor Used To Treat Pain And Inflammation. It Also Induces Apoptosis In Hepatoma Cells And Indirectly Activates Sirt1, Each

Cytochrome C Binding Agent That Inhibits Electron Transport Chain Activity, Oxidative Phosphorylation, And Atp Synthesis, Each

Rig1-Like Receptor Antagonist Found In Andrographis. It Decreases Tnf-A-Induced Generation Of Ros, Suppresses Development Of Diabetes, And Inhibits Hsp90 Activity And Induces Apoptosis In Leukemia Cells, Each

Endogenous Clr-Ramp2/3 Receptor Agonist Involved In Cell Growth And Differentiation. It Decreases Blood Pressure, Increases Neovascularization, And Binds Microtubule-Associated Proteins In The Cytoskeleton, Each

Rig1-Like Receptor Antagonist Found In Andrographis. It Decreases Tnf-A-Induced Generation Of Ros, Suppresses Development Of Diabetes, And Inhibits Hsp90 Activity And Induces Apoptosis In Leukemia Cells, Each

Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each

Prodrug Of 5-Fu And Inhibitor Of Thymidylate Synthase That Is Used To Treat Various Cancers. It Inhibits Dna Synthesis, Each

Pp1/2A Inhibitor Found In Canarthis Vesicatoria. It Inhibits Proliferation Of Colorectal Cancer Cells, Increases Mcp-1, Il-6, And Il-1Ss Levels, And Inhibits Differentiation And Resorptive Activity Of Osteoclasts, Each

Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each

Rig1-Like Receptor Antagonist Found In Andrographis. It Decreases Tnf-A-Induced Generation Of Ros, Suppresses Development Of Diabetes, And Inhibits Hsp90 Activity And Induces Apoptosis In Leukemia Cells, Each

Endogenous Clr-Ramp2/3 Receptor Agonist Involved In Cell Growth And Differentiation. It Decreases Blood Pressure, Increases Neovascularization, And Binds Microtubule-Associated Proteins In The Cytoskeleton, Each

Aromatase Inhibitor Used To Treat Er-Positive Breast Cancer. It Suppresses Estrogen Synthesis And Induces Apoptosis In Breast Cancer Cells, Each

Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each

Prodrug Of 5-Fu And Inhibitor Of Thymidylate Synthase That Is Used To Treat Various Cancers. It Inhibits Dna Synthesis, Each

Pp1/2A Inhibitor Found In Canarthis Vesicatoria. It Inhibits Proliferation Of Colorectal Cancer Cells, Increases Mcp-1, Il-6, And Il-1Ss Levels, And Inhibits Differentiation And Resorptive Activity Of Osteoclasts, Each

Aromatase Inhibitor Used To Treat Er-Positive Breast Cancer. It Suppresses Estrogen Synthesis And Induces Apoptosis In Breast Cancer Cells, Each

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