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G418 Disulfate is an aminoglycoside antibiotic similar in structure to gentamicin B1 and blocks polypeptide synthesis by inhibiting the elongation step in both prokaryotic and eukaryotic cells.
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Gabexate mesylate could inhibit trypsin, plasmin, plasma kallikrein and thrombin with IC50s of 9.4 μM, 30 μM, 41 μM and 110 μM. It has certain anticoagulant effect.
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Gabexate mesylate could inhibit trypsin, plasmin, plasma kallikrein and thrombin with IC50s of 9.4 μM, 30 μM, 41 μM and 110 μM. It has certain anticoagulant effect.
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CSNpharm
Gabexate mesylate could inhibit trypsin, plasmin, plasma kallikrein and thrombin with IC50s of 9.4 μM, 30 μM, 41 μM and 110 μM. It has certain anticoagulant effect.
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CSNpharm
Gabexate mesylate could inhibit trypsin, plasmin, plasma kallikrein and thrombin with IC50s of 9.4 μM, 30 μM, 41 μM and 110 μM. It has certain anticoagulant effect.
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CSNpharm
Gabexate mesylate could inhibit trypsin, plasmin, plasma kallikrein and thrombin with IC50s of 9.4 μM, 30 μM, 41 μM and 110 μM. It has certain anticoagulant effect.
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Gaboxadol HCl is a systemically active GABAA receptor agonist and GABAA-ρ receptor antagonist. Displays antinociceptive, anticonvulsant and sedative effects. Hypnotic agent that enhances delta activity within non-REM sleep in rats.
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Gaboxadol HCl is a systemically active GABAA receptor agonist and GABAA-ρ receptor antagonist. Displays antinociceptive, anticonvulsant and sedative effects. Hypnotic agent that enhances delta activity within non-REM sleep in rats.
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Gadobutrol is used in magnetic resonance imaging (MRI) imaging to help visualize and detect vascular abnormalities in the blood brain barrier and central nervous system.
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Gadobutrol is used in magnetic resonance imaging (MRI) imaging to help visualize and detect vascular abnormalities in the blood brain barrier and central nervous system.
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Gadobutrol is used in magnetic resonance imaging (MRI) imaging to help visualize and detect vascular abnormalities in the blood brain barrier and central nervous system.
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CSNpharm
Gadobutrol is used in magnetic resonance imaging (MRI) imaging to help visualize and detect vascular abnormalities in the blood brain barrier and central nervous system.
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CSNpharm
Gadobutrol is used in magnetic resonance imaging (MRI) imaging to help visualize and detect vascular abnormalities in the blood brain barrier and central nervous system.
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CSNpharm
Gadobutrol is used in magnetic resonance imaging (MRI) imaging to help visualize and detect vascular abnormalities in the blood brain barrier and central nervous system.
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Gadodiamide is a gadolinium-based MRI contrast agent, used in MR imaging procedures to assist in the visualization of blood vessels.
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Gadodiamide is a gadolinium-based MRI contrast agent, used in MR imaging procedures to assist in the visualization of blood vessels.
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Gadolinium(III) chloride hexahydrate can inhibit macrophages and significantly decrease NO production and inducible INOS expression in rat lung macrophages.
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Gadolinium(III) chloride hexahydrate can inhibit macrophages and significantly decrease NO production and inducible INOS expression in rat lung macrophages.
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Gadopentetate Dimeglumine is complex of gadolinium with a chelating agent, diethylenetriamine penta-acetic acid (DTPA), used during an MRI (magnetic resonance imaging) test.
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Gadopentetate Dimeglumine is complex of gadolinium with a chelating agent, diethylenetriamine penta-acetic acid (DTPA), used during an MRI (magnetic resonance imaging) test.
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Gadopentetate Dimeglumine is complex of gadolinium with a chelating agent, diethylenetriamine penta-acetic acid (DTPA), used during an MRI (magnetic resonance imaging) test.
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GAK inhibitor 49 ATP-competitive inhibitor of cyclin G associated kinase (GAK) with Ki of 0.54 nM and IC50 of 56 nM. It also binds to RIPK2.
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GAK inhibitor 49 ATP-competitive inhibitor of cyclin G associated kinase (GAK) with Ki of 0.54 nM and IC50 of 56 nM. It also binds to RIPK2.
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GAK inhibitor 49 ATP-competitive inhibitor of cyclin G associated kinase (GAK) with Ki of 0.54 nM and IC50 of 56 nM. It also binds to RIPK2.
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GAK inhibitor 49 ATP-competitive inhibitor of cyclin G associated kinase (GAK) with Ki of 0.54 nM and IC50 of 56 nM. It also binds to RIPK2.
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GAK inhibitor 49 ATP-competitive inhibitor of cyclin G associated kinase (GAK) with Ki of 0.54 nM and IC50 of 56 nM. It also binds to RIPK2.
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Galangin functions as an antagonist of the aryl hydrocarbon receptor and also inhibits CYP1A1 (IC50 = 1 μM). It belongs to flavonoids and can be extracted from the rhizome of Zingiber officinale Roscoe with anti-inflammatory properties.
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Galangin functions as an antagonist of the aryl hydrocarbon receptor and also inhibits CYP1A1 (IC50 = 1 μM). It belongs to flavonoids and can be extracted from the rhizome of Zingiber officinale Roscoe with anti-inflammatory properties.
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Galangin functions as an antagonist of the aryl hydrocarbon receptor and also inhibits CYP1A1 (IC50 = 1 μM). It belongs to flavonoids and can be extracted from the rhizome of Zingiber officinale Roscoe with anti-inflammatory properties.
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Galangin functions as an antagonist of the aryl hydrocarbon receptor and also inhibits CYP1A1 (IC50 = 1 μM). It belongs to flavonoids and can be extracted from the rhizome of Zingiber officinale Roscoe with anti-inflammatory properties.
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Galanthamine is a long-acting, centrally active acetylcholinesterase (AChE) inhibitor (IC50 = 410 nM) and allosteric potentiator at neuronal nicotinic ACh receptors.
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Galanthamine is a long-acting, centrally active acetylcholinesterase (AChE) inhibitor (IC50 = 410 nM) and allosteric potentiator at neuronal nicotinic ACh receptors.
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Galanthamine hydrobromide is a natural occuring AchE inhibitor with IC50 value of 410nM and allosteric potentiator at neuronal nAchRs, used for the treatment of cognitive decline in mild to moderate Alzheimer’s disease and various other memory impairments.
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Galanthamine hydrobromide is a natural occuring AchE inhibitor with IC50 value of 410nM and allosteric potentiator at neuronal nAchRs, used for the treatment of cognitive decline in mild to moderate Alzheimer’s disease and various other memory impairments.
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Galantamine is a competitive and reversible cholinesterase (AChE) inhibitor and is used for the treatment of mild to moderate Alzheimer’s disease and various other memory impairments.
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Galantamine is a competitive and reversible cholinesterase (AChE) inhibitor and is used for the treatment of mild to moderate Alzheimer’s disease and various other memory impairments.
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Galantamine is a competitive and reversible cholinesterase (AChE) inhibitor and is used for the treatment of mild to moderate Alzheimer’s disease and various other memory impairments.
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Galantamine is a competitive and reversible cholinesterase (AChE) inhibitor and is used for the treatment of mild to moderate Alzheimer’s disease and various other memory impairments.
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Galegine is a toxic chemical compound that has been isolated from Goat’s rue (Galega officinalis), it was used as a drug for diabetes in the 1920s.
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Galegine is a toxic chemical compound that has been isolated from Goat’s rue (Galega officinalis), it was used as a drug for diabetes in the 1920s.
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CSNpharm
Galegine is a toxic chemical compound that has been isolated from Goat’s rue (Galega officinalis), it was used as a drug for diabetes in the 1920s.
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CSNpharm
Galegine is a toxic chemical compound that has been isolated from Goat’s rue (Galega officinalis), it was used as a drug for diabetes in the 1920s.
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