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Reference: CDX-G0197-M005
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(-)-Gallocatechin gallate is a catechin polyphenol that has been found in green tea extracts. It has been shown to have diverse biological activities, including antioxidant, antiallergic, antiobesity and anticancer...
Reference: CDX-E0128-M010
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(-)-Epigallocatechin gallate (EGCG), an antioxidant and anti-inflammatory polyphenol flavonoid exerts antitumor properties by inhibiting telomerase and DNA methyltransferase activity. EGCG inhibits the expression of...
Reference: AG-CN2-0063-M100
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Potent anticancer compound. Anti-angiogenic. VEGF, VE-cadherin phosphorylation, matrix metalloproteinase and urokinase-plasminogen activator (uPA) inhibitor. Anti-inflammatory. NF-kappaB inhibitor. Modulates chronic...
Reference: AG-CN2-0063-M025
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Potent anticancer compound. Anti-angiogenic. VEGF, VE-cadherin phosphorylation, matrix metalloproteinase and urokinase-plasminogen activator (uPA) inhibitor. Anti-inflammatory. NF-kappaB inhibitor. Modulates chronic...
Reference: CDX-E0182-M010
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(-)-Epigallocatechin ((-)-EGC) is a major green tea polyphenol with antioxidant, anti-inflammatory and anticancer activities. It has been shown to scavenge DPPH radicals and to prevent the growth of several different...
Reference: CDX-E0181-M010
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The catechins (-)-epicatechin (EC) and (-)-epigallocatechin gallate (EGCG) are abundant in green and black teas. (-)-Epicatechin gallate (ECG) is a natural catechin with a single galloyl group. Like EGCG, it inhibits...
Reference: CDX-E0231-M025
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Epicatechin is a natural flavonoid found in green tea. It has been reported to possess an immense antioxidant effect which contributes to its therapeutic effect in diabetes and cancer conditions. The consumption of...
Reference: CDX-E0231-M005
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Epicatechin is a natural flavonoid found in green tea. It has been reported to possess an immense antioxidant effect which contributes to its therapeutic effect in diabetes and cancer conditions. The consumption of...
Reference: CDX-C0228-G005
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Pyridine-like alkaloid. Nicotine agonist. Potent agonist at alpha3beta4 and alpha7 nicotinic acetylcholine receptors and partial agonist at alpha4beta2 nicotinic acetylcholine receptors. Shows analgesic,...
Reference: CDX-C0228-M500
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Pyridine-like alkaloid. Nicotine agonist. Potent agonist at alpha3beta4 and alpha7 nicotinic acetylcholine receptors and partial agonist at alpha4beta2 nicotinic acetylcholine receptors. Shows analgesic,...
Reference: CDX-C0228-M100
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Pyridine-like alkaloid. Nicotine agonist. Potent agonist at alpha3beta4 and alpha7 nicotinic acetylcholine receptors and partial agonist at alpha4beta2 nicotinic acetylcholine receptors. Shows analgesic,...
Reference: CDX-C0453-M025
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Catechins have wide biological functionality, including antioxidant, anti-inflammatory, antiviral and anticancer activities. Catechins also play a key role in regulating carbohydrate and lipid metabolism. (-)-Catechin...
Reference: CDX-C0453-M005
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Catechins have wide biological functionality, including antioxidant, anti-inflammatory, antiviral and anticancer activities. Catechins also play a key role in regulating carbohydrate and lipid metabolism. (-)-Catechin...
Reference: CDX-C0144-G010
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Chirality inducing agent. Useful tool as resolving agent to separate the isomers and purify racemic mixtures (e.g. DL-lysine) by fractionally crystallizing the product to obtain the pure isomer (e.g. D-lysine). Can...
Reference: CDX-C0144-G001
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Chirality inducing agent. Useful tool as resolving agent to separate the isomers and purify racemic mixtures (e.g. DL-lysine) by fractionally crystallizing the product to obtain the pure isomer (e.g. D-lysine). Can...
Reference: CDX-B0240-M100
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(-)-Bicuculline methiodide is the N-methylated water-soluble derivative of the widely-employed ionotropic GABAA receptor antagonist (+)-Bicuculline. This prototypic, competitive GABAA receptor antagonist displaces...
Reference: CDX-B0240-M025
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(-)-Bicuculline methiodide is the N-methylated water-soluble derivative of the widely-employed ionotropic GABAA receptor antagonist (+)-Bicuculline. This prototypic, competitive GABAA receptor antagonist displaces...
Reference: AG-CN2-0532-M050
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Metabolizes into (-)-Arctigenin (AG-CN2-0530). Multifunctional natural compound with photoprotective, anti-inflammatory, antidiabetic, antiproliferative and antiviral activities. Decreasing the production of nitric...
Reference: AG-CN2-0532-M010
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Metabolizes into (-)-Arctigenin (AG-CN2-0530). Multifunctional natural compound with photoprotective, anti-inflammatory, antidiabetic, antiproliferative and antiviral activities. Decreasing the production of nitric...
Reference: AG-CN2-0530-M050
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Aglycone metabolite of (-)-Arctiin (AG-CN2-0532), isolated from Arctium lappa. Multifunctional natural compound with antioxidant, antibacterial, anti-inflammatory, antidiabetic, neuroprotective, antiproliferative and...
Reference: AG-CN2-0530-M010
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Aglycone metabolite of (-)-Arctiin (AG-CN2-0532), isolated from Arctium lappa. Multifunctional natural compound with antioxidant, antibacterial, anti-inflammatory, antidiabetic, neuroprotective, antiproliferative and...
Reference: AG-CN2-0016-M001
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Quaternary ammonium compound. Antifouling compound. Inhibits biofilm formation but not bacterial growth of Staphylococcus epidermidis. Anticancer compound. Cytotoxic against L5178Y mouse lymphoma cells.
Reference: AG-CR1-3627-G005
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alpha1-Adrenergic receptor (alpha-AR) antagonist. Prototypical calcium channel protein inhibitor that blocks the L-type Ca2+ channels in smooth and cardiac muscle cells. Vasodilator known to reduce the renal clearance...
Reference: AG-CR1-3627-G001
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alpha1-Adrenergic receptor (alpha-AR) antagonist. Prototypical calcium channel protein inhibitor that blocks the L-type Ca2+ channels in smooth and cardiac muscle cells. Vasodilator known to reduce the renal clearance...
Reference: AG-CR1-3627-M100
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alpha1-Adrenergic receptor (alpha-AR) antagonist. Prototypical calcium channel protein inhibitor that blocks the L-type Ca2+ channels in smooth and cardiac muscle cells. Vasodilator known to reduce the renal clearance...
Reference: CDX-H0117-M050
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Synthetic methylxanthine metabolite of pentoxifylline. Potent anti-inflammatory agent in which only the (−) optical isomer is biologically active. Inhibits the generation of phosphatidic acid from cytokine-activated...
Reference: CDX-H0117-M010
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Synthetic methylxanthine metabolite of pentoxifylline. Potent anti-inflammatory agent in which only the (−) optical isomer is biologically active. Inhibits the generation of phosphatidic acid from cytokine-activated...
Reference: CDX-D0442-M050
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Flavanonol derived from plant source. Precursor of kaempferol. Shown to stimulate glucose uptake and improve insulin resistance by inducing adipogenesis through increased PPAR2 expression. Anti-inflammatory compound.
Reference: CDX-D0442-M010
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Flavanonol derived from plant source. Precursor of kaempferol. Shown to stimulate glucose uptake and improve insulin resistance by inducing adipogenesis through increased PPAR2 expression. Anti-inflammatory compound.
Reference: AG-CR1-2904-M005
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Stable synthetic cerulenin derivative. Competitive irreversible fatty acid synthase (FASN) inhibitor that acts on KR, ACP and TE domains. Used to study fatty acid synthesis in metabolic disorders and cancer. Useful...
Reference: AG-CR1-2904-M001
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Stable synthetic cerulenin derivative. Competitive irreversible fatty acid synthase (FASN) inhibitor that acts on KR, ACP and TE domains. Used to study fatty acid synthesis in metabolic disorders and cancer. Useful...
Reference: BVT-0026-M001
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Angucyclinone antibiotic. Antibacterial and antitumor agent. Potentiates the cytotoxicity of vincristine. Antimalarial agent.
Reference: SYN-3004-M100
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(+)-JQ1 is a potent, high affinity, selective BET bromodomain inhibitor (IC(50) values of 17.7, 32.6, 76.9 and 12942nM respectively for BRD2 (N-terminal (N)), BRD4 (C-terminal (C)), BRD4 (N) and CREBBP, respectively....
Reference: SYN-3004-M050
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(+)-JQ1 is a potent, high affinity, selective BET bromodomain inhibitor (IC(50) values of 17.7, 32.6, 76.9 and 12942nM respectively for BRD2 (N-terminal (N)), BRD4 (C-terminal (C)), BRD4 (N) and CREBBP, respectively....
Reference: SYN-3004-M010
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(+)-JQ1 is a potent, high affinity, selective BET bromodomain inhibitor (IC(50) values of 17.7, 32.6, 76.9 and 12942nM respectively for BRD2 (N-terminal (N)), BRD4 (C-terminal (C)), BRD4 (N) and CREBBP, respectively....
Reference: SYN-3004-M005
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(+)-JQ1 is a potent, high affinity, selective BET bromodomain inhibitor (IC(50) values of 17.7, 32.6, 76.9 and 12942nM respectively for BRD2 (N-terminal (N)), BRD4 (C-terminal (C)), BRD4 (N) and CREBBP, respectively....
Reference: SYN-3004-M001
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(+)-JQ1 is a potent, high affinity, selective BET bromodomain inhibitor (IC(50) values of 17.7, 32.6, 76.9 and 12942nM respectively for BRD2 (N-terminal (N)), BRD4 (C-terminal (C)), BRD4 (N) and CREBBP, respectively....
Reference: BVT-0279-M001
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Phytotoxin (Fruit rot toxin). Antibiotic. Antibacterial and antifungal compound.
Reference: AG-CR1-3688-M025
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Irreversible inhibitor of carnitine palmitoyltransferase-1 (CPT-1a) a mitochondrial enzyme involved in fatty acid beta-oxidation. CPR-1a on the outer face of the inner mitochondrial membrane, consequently prevents the...
Reference: AG-CR1-3688-M005
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Irreversible inhibitor of carnitine palmitoyltransferase-1 (CPT-1a) a mitochondrial enzyme involved in fatty acid beta-oxidation. CPR-1a on the outer face of the inner mitochondrial membrane, consequently prevents the...
Reference: AG-CN2-0407-G001
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Specific histidine decarboxylase inhibitor. Anti-inflammatory. COX-1 inhibitor. Antioxidant flavonoid. Free radical scavenger. Inhibits lipid peroxidation. Antimetastatic and anticancer compound. Antiangiogenic....
Reference: AG-CN2-0407-M500
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Specific histidine decarboxylase inhibitor. Anti-inflammatory. COX-1 inhibitor. Antioxidant flavonoid. Free radical scavenger. Inhibits lipid peroxidation. Antimetastatic and anticancer compound. Antiangiogenic....
Reference: CDX-C0169-G500
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Terpene standard for GC.
Reference: CDX-C0169-G100
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Terpene standard for GC.
Reference: CDX-C0169-G005
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Terpene standard for GC.
Reference: BVT-0190-M001
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Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor Reviews.
Reference: AG-CN2-0018-M025
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Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
Reference: AG-CN2-0018-M010
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Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
Reference: AG-CN2-0018-M005
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Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
Reference: CDX-B0145-M250
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Biotin succinimidyl ester is the most popular amine-reactive biotinylating agent for modifying proteins, peptides, antibodies, oligonucleotides, microbeads and other biological molecules. It forms irreversible amide...
Reference: CDX-B0145-M100
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Biotin succinimidyl ester is the most popular amine-reactive biotinylating agent for modifying proteins, peptides, antibodies, oligonucleotides, microbeads and other biological molecules. It forms irreversible amide...
Reference: CDX-B0239-G005
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GABAA receptor antagonist.
Reference: CDX-B0239-M500
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GABAA receptor antagonist.
Reference: CDX-B0239-M025
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GABAA receptor antagonist.
Reference: BVT-0307-M025
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Phytotoxin. Antibiotic. Antiviral and antineoplastic agent. Antileishmanial agent. Reversible inhibitor of eukaryotic nuclear DNA replication. Useful for cell synchronization. Blocks the cell cycle at G1/S phase....
Reference: BVT-0307-M005
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Phytotoxin. Antibiotic. Antiviral and antineoplastic agent. Antileishmanial agent. Reversible inhibitor of eukaryotic nuclear DNA replication. Useful for cell synchronization. Blocks the cell cycle at G1/S phase....
Reference: BVT-0307-M001
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Phytotoxin. Antibiotic. Antiviral and antineoplastic agent. Antileishmanial agent. Reversible inhibitor of eukaryotic nuclear DNA replication. Useful for cell synchronization. Blocks the cell cycle at G1/S phase....

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