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Showing 241 to 242 of 20 results

Product	Utech#	UOM	Mfg#	Price
Cytochrome C Binding Agent That Inhibits Electron Transport Chain Activity, Oxidative Phosphorylation, And Atp Synthesis, Each	5583596	EA	A5378-50 mg	$ 685.85
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	$ 58.24
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	$ 101.13
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	$ 108.28
Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each	5583720	EA	C2845-5 g	$ 76.54
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	$ 157.07
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	$ 162.92
Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each	5583918	EA	C2845-10 g	$ 110.50
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	$ 198.03
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	$ 290.25
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	$ 295.10
Protein Translation And Peptidyl Transferase Inhibitor. It Is Particularly Active Against Streptomyces, Each	5584325	EA	C2845-50 g	$ 212.40
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	$ 471.71
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	$ 477.53
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	$ 542.72
Pde4 Inhibitor Used To Treat Psoriasis And Psoriatic Arthritis. It Also Decreases Levels Of Inos, Il-23, And Tnf-A, Each	5584453	EA	A6269-5 mg	$ 339.71
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	5584720	EA	A1607-500 mg	$ 1,109.55
Prodrug Of 5-Fu And Inhibitor Of Thymidylate Synthase That Is Used To Treat Various Cancers. It Inhibits Dna Synthesis, Each	5584800	EA	C0162-5 g	$ 1,509.76
Aromatase Inhibitor Used To Treat Er-Positive Breast Cancer. It Suppresses Estrogen Synthesis And Induces Apoptosis In Breast Cancer Cells, Each	5584821	EA	A5302-1 g	$ 1,649.51
Pde4 Inhibitor Used To Treat Psoriasis And Psoriatic Arthritis. It Also Decreases Levels Of Inos, Il-23, And Tnf-A, Each	5584830	EA	A6269-25 mg	$ 970.58

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

Pde4 Inhibitor Used To Treat Psoriasis And Psoriatic Arthritis. It Also Decreases Levels Of Inos, Il-23, And Tnf-A, 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

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

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

Pde4 Inhibitor Used To Treat Psoriasis And Psoriatic Arthritis. It Also Decreases Levels Of Inos, Il-23, And Tnf-A, Each

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