Category: Reagents

Reference: AG-CN2-0076-M001
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Potent competitive gamma-aminobutyric acid type A (GABAA) receptor antagonist and glycine receptor agonist. Weak nicotinic acetylcholine receptor agonist. Muscle relaxant. Anti-inflammatory. Has analgesic properties....
Reference: AG-CN2-0076-M005
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Potent competitive gamma-aminobutyric acid type A (GABAA) receptor antagonist and glycine receptor agonist. Weak nicotinic acetylcholine receptor agonist. Muscle relaxant. Anti-inflammatory. Has analgesic properties....
Reference: AG-CN2-0076-M025
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Potent competitive gamma-aminobutyric acid type A (GABAA) receptor antagonist and glycine receptor agonist. Weak nicotinic acetylcholine receptor agonist. Muscle relaxant. Anti-inflammatory. Has analgesic properties....
Reference: AG-CN2-0077-M010
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Noncaloric natural sweetener, 300 times more potent than sucrose. Antidiabetic. Antihyperglycaemic and antihypoglycaemic. Potentiates insulin secretion. Enhances acetyl-CoA carboxylase (ACC) gene expression. Increases...
Reference: AG-CN2-0077-M050
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Noncaloric natural sweetener, 300 times more potent than sucrose. Antidiabetic. Antihyperglycaemic and antihypoglycaemic. Potentiates insulin secretion. Enhances acetyl-CoA carboxylase (ACC) gene expression. Increases...
Reference: AG-CN2-0079-M100
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Potent immunosuppressant (same as FK-506 (Prod. No. AG-CN2-0047) and rapamycin (Prod. No. AG-CN2-0025)). Forms a complex with cyclophilin. Inhibits the activity of the calcium/calmodulin-dependent protein phosphatase...
Reference: AG-CN2-0079-5100
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Potent immunosuppressant (same as FK-506 (Prod. No. AG-CN2-0047) and rapamycin (Prod. No. AG-CN2-0025)). Forms a complex with cyclophilin. Inhibits the activity of the calcium/calmodulin-dependent protein phosphatase...
Reference: AG-CN2-0079-G001
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Potent immunosuppressant (same as FK-506 (Prod. No. AG-CN2-0047) and rapamycin (Prod. No. AG-CN2-0025)). Forms a complex with cyclophilin. Inhibits the activity of the calcium/calmodulin-dependent protein phosphatase...
Reference: AG-CN2-0080-M010
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Antibacterial. Human collagen I synthesis inducer. Anti-wrinkle activity. Shows wound healing activity. Enhances normal human skin cell migration, attachment and growth. Suppresses collagen expression and...
Reference: AG-CN2-0080-M050
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Antibacterial. Human collagen I synthesis inducer. Anti-wrinkle activity. Shows wound healing activity. Enhances normal human skin cell migration, attachment and growth. Suppresses collagen expression and...
Reference: AG-CN2-0082-M001
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Negative control for phorbol ester activation of protein kinase C and studies with PMA (AG-CN2-0010). Might be a reasonable PKC-independent TRPV4 channels agonist.
Reference: AG-CN2-0083-C100
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Antifungal and antifertility compound. Antitumor compound. PPARalpha signaling agonist. Angiogenesis inhibitor. Apoptosis and autophagy inducer. Microtubule-destabilizing agent. Anti-inflammatory. Inhibits NF-kappaB...
Reference: AG-CN2-0083-M001
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Antifungal and antifertility compound. Antitumor compound. PPARalpha signaling agonist. Angiogenesis inhibitor. Apoptosis and autophagy inducer. Microtubule-destabilizing agent. Anti-inflammatory. Inhibits NF-kappaB...
Reference: AG-CN2-0084-M001
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Anticancer compound. Apoptosis inducer. Induces DNA fragmentation at the G1/S phase of the cell cycle. HIV-1 replication inhibitor. Anti-inflammatory. Vasodilatation inducer. Increases BMP-2 expression (mRNA) and...
Reference: AG-CN2-0084-M005
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Anticancer compound. Apoptosis inducer. Induces DNA fragmentation at the G1/S phase of the cell cycle. HIV-1 replication inhibitor. Anti-inflammatory. Vasodilatation inducer. Increases BMP-2 expression (mRNA) and...
Reference: AG-CN2-0084-M025
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Anticancer compound. Apoptosis inducer. Induces DNA fragmentation at the G1/S phase of the cell cycle. HIV-1 replication inhibitor. Anti-inflammatory. Vasodilatation inducer. Increases BMP-2 expression (mRNA) and...
Reference: AG-CN2-0085-M010
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Offensive principle of the so-called "headache tree". Causes a painful cold sensation. Selective TRPA1 activator. Weak TRPM8 activator. Releases CGRP (calcitonin gene-related peptide) after TRPA1 activation which...
Reference: AG-CN2-0086-M001
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Wide range of tyrosine and serine/threonine protein kinase inhibitor, including Syk, p56lck, PKA, PKC, MLCK, CDPK, JNK and PI3K. Inhibits the tyrosine phosphorylation of STAT3 and STAT5. Potent apoptosis inducer....
Reference: AG-CN2-0086-M005
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Wide range of tyrosine and serine/threonine protein kinase inhibitor, including Syk, p56lck, PKA, PKC, MLCK, CDPK, JNK and PI3K. Inhibits the tyrosine phosphorylation of STAT3 and STAT5. Potent apoptosis inducer....
Reference: AG-CN2-0086-M025
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Wide range of tyrosine and serine/threonine protein kinase inhibitor, including Syk, p56lck, PKA, PKC, MLCK, CDPK, JNK and PI3K. Inhibits the tyrosine phosphorylation of STAT3 and STAT5. Potent apoptosis inducer....
Reference: AG-CN2-0087-M001
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Antiprotozoal. Potent inhibitor of histone deacetylase (HDAC). Inhibits proliferation. Induces cell cycle arrest at the G1 phase. Induces hyperacetylation of histone H4. Apoptosis inducer. Potent anti-angiogenic...
Reference: AG-CN2-0087-M005
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Antiprotozoal. Potent inhibitor of histone deacetylase (HDAC). Inhibits proliferation. Induces cell cycle arrest at the G1 phase. Induces hyperacetylation of histone H4. Apoptosis inducer. Potent anti-angiogenic...
Reference: AG-CN2-0089-M001
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Potent, cell permeable adenylyl cyclase activator. Increases intracellular cAMP levels. Widely used tool to investigate cAMP as a second messenger. Inotropic and antihypertensive. Smooth muscle relaxant/vasodilator....
Reference: AG-CN2-0089-M005
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Potent, cell permeable adenylyl cyclase activator. Increases intracellular cAMP levels. Widely used tool to investigate cAMP as a second messenger. Inotropic and antihypertensive. Smooth muscle relaxant/vasodilator....
Reference: AG-CN2-0089-M025
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Potent, cell permeable adenylyl cyclase activator. Increases intracellular cAMP levels. Widely used tool to investigate cAMP as a second messenger. Inotropic and antihypertensive. Smooth muscle relaxant/vasodilator....
Reference: AG-CN2-0089-M050
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Potent, cell permeable adenylyl cyclase activator. Increases intracellular cAMP levels. Widely used tool to investigate cAMP as a second messenger. Inotropic and antihypertensive. Smooth muscle relaxant/vasodilator....
Reference: AG-CN2-0090-M001
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Shows calcium-antagonistic and vasorelaxant activity. Antibacterial. Anti-inflammatory. Potent COX-2 and inducible nitric oxide (iNOS; NOS II) inhibitor. Hepatoprotective. Anticancer compound. Apoptosis inducer....
Reference: AG-CN2-0092-C250
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Mycotoxin. Potent and selective competitive protein phosphatase 2A (PP2A) inhibitor. Does not inhibit PP1, PP2B, PTP1B, ALP and CIP. Antitumor agent. Antimetastatic.
Reference: AG-CN2-0092-C500
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Mycotoxin. Potent and selective competitive protein phosphatase 2A (PP2A) inhibitor. Does not inhibit PP1, PP2B, PTP1B, ALP and CIP. Antitumor agent. Antimetastatic.
Reference: AG-CN2-0093-C250
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Potent and selective protein phosphatase 2A (PP2A) inhibitor. Cell adhesion inhibitor. Inhibits the adhesion of B16 melanoma cells to laminin and collagen type IV in a dose dependent manner but not to fibronectin....
Reference: AG-CN2-0098-M005
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Anticancer and antimetastatic. alpha-Glucosidase inhibitor. Topoisomerase I Inhibitor. Apoptosis inducer. Anti-inflammatory. 15-Lipoxygenase (15-LOX) inhibitor. IL-6 production inhibitor. Fatty acid synthase (FAS)...
Reference: AG-CN2-0098-M025
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Anticancer and antimetastatic. alpha-Glucosidase inhibitor. Topoisomerase I Inhibitor. Apoptosis inducer. Anti-inflammatory. 15-Lipoxygenase (15-LOX) inhibitor. IL-6 production inhibitor. Fatty acid synthase (FAS)...
Reference: AG-CN2-0102-C250
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Shows strong gastrointestinal motor stimulating (GMS) activity. Motilin receptor agonist. Stimulates smooth muscle cell contraction. Stimulates cholinergic neurons in a non-vagal pathway. Enhances gastrointestinal...
Reference: AG-CN2-0102-M001
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Shows strong gastrointestinal motor stimulating (GMS) activity. Motilin receptor agonist. Stimulates smooth muscle cell contraction. Stimulates cholinergic neurons in a non-vagal pathway. Enhances gastrointestinal...
Reference: AG-CN2-0104-C100
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Induces neuritogenesis. Potent and selective irreversible proteasome inhibitor. Specifically inhibits 20S proteasome (MCP; multicatalytic complex). Blocks proteasome activity by targeting the catalytic beta-subunit....
Reference: AG-CN2-0104-C200
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Induces neuritogenesis. Potent and selective irreversible proteasome inhibitor. Specifically inhibits 20S proteasome (MCP; multicatalytic complex). Blocks proteasome activity by targeting the catalytic beta-subunit....
Reference: AG-CN2-0104-C500
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Induces neuritogenesis. Potent and selective irreversible proteasome inhibitor. Specifically inhibits 20S proteasome (MCP; multicatalytic complex). Blocks proteasome activity by targeting the catalytic beta-subunit....
Reference: AG-CN2-0104-M001
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Induces neuritogenesis. Potent and selective irreversible proteasome inhibitor. Specifically inhibits 20S proteasome (MCP; multicatalytic complex). Blocks proteasome activity by targeting the catalytic beta-subunit....
Reference: AG-CN2-0109-M001
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Diacylglycerol acyltransferase (DGAT) inhibitor. Excessive accumulation of triacetylglycerol produced by DGAT may cause fatty liver, obesity and hypertriglyceridemia, which may lead to atherosclerosis, diabetes and...
Reference: AG-CN2-0109-MM25
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Diacylglycerol acyltransferase (DGAT) inhibitor. Excessive accumulation of triacetylglycerol produced by DGAT may cause fatty liver, obesity and hypertriglyceridemia, which may lead to atherosclerosis, diabetes and...
Reference: AG-CN2-0110-M001
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Diacylglycerol acyltransferase (DGAT) inhibitor. Excessive accumulation of triacetylglycerol produced by DGAT may cause fatty liver, obesity and hypertriglyceridemia, which may lead to atherosclerosis, diabetes and...
Reference: AG-CN2-0110-MM25
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Diacylglycerol acyltransferase (DGAT) inhibitor. Excessive accumulation of triacetylglycerol produced by DGAT may cause fatty liver, obesity and hypertriglyceridemia, which may lead to atherosclerosis, diabetes and...
Reference: AG-CN2-0111-M001
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Phytotoxin. Potent and specific PKC inhibitor. Competes for the phorbol binding site. Anticancer compound. Cytotoxic. Antiproliferative. Antiparasitic. Antimicrobial.
Reference: AG-CN2-0111-M005
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Phytotoxin. Potent and specific PKC inhibitor. Competes for the phorbol binding site. Anticancer compound. Cytotoxic. Antiproliferative. Antiparasitic. Antimicrobial.
Reference: AG-CN2-0115-C250
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Phytotoxin. Derivative of HDAC inhibitor chlamydocin Similar chemical structure to the TAN-1746 compounds (potent HDAC inhibitors).
Reference: AG-CN2-0115-M001
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Phytotoxin. Derivative of HDAC inhibitor chlamydocin Similar chemical structure to the TAN-1746 compounds (potent HDAC inhibitors).
Reference: AG-CN2-0117-C250
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Antifungal. Anticancer compound. Cytotoxic to human cancer cell lines.
Reference: AG-CN2-0117-M001
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Antifungal. Anticancer compound. Cytotoxic to human cancer cell lines.
Reference: AG-CN2-0119-C250
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Antifungal. Antibacterial against Gram-positive bacteria.
Reference: AG-CN2-0119-M001
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Antifungal. Antibacterial against Gram-positive bacteria.
Reference: AG-CN2-0120-C250
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Peptide with lasso structure. Antimycobacterial.
Reference: AG-CN2-0120-M001
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Peptide with lasso structure. Antimycobacterial.
Reference: AG-CN2-0121-C250
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Antibacterial. Selectively inhibits a Hof1 deletion strain.
Reference: AG-CN2-0121-M001
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Antibacterial. Selectively inhibits a Hof1 deletion strain.
Reference: AG-CN2-0122-C250
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Plant growth inhibitor. Acyl-CoA-cholesterol acyltransferase (ACAT) inhibitor. Anticancer compound. Cytotoxic. Non-peptidic oxytocin receptor antagonist. Calpain inhibitor.
Reference: AG-CN2-0122-M001
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Plant growth inhibitor. Acyl-CoA-cholesterol acyltransferase (ACAT) inhibitor. Anticancer compound. Cytotoxic. Non-peptidic oxytocin receptor antagonist. Calpain inhibitor.
Reference: AG-CN2-0125-C250
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Acyl-CoA:cholesterol acyltransferase (ACAT) isozymes ACAT1 and ACAT2 inhibitor. Tremorgenic. Cholesteryl ester (CE) synthesis inhibitor.
Reference: AG-CN2-0125-M001
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Acyl-CoA:cholesterol acyltransferase (ACAT) isozymes ACAT1 and ACAT2 inhibitor. Tremorgenic. Cholesteryl ester (CE) synthesis inhibitor.
Reference: AG-CN2-0127-C250
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Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. Mitotic kinesin Eg5 (Mitotic Kinesin Spindle Protein; KSP) inhibitor. Specific M phase inhibitor.
Reference: AG-CN2-0131-C250
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Specific anti-mycobacterial. Inhibits growth of Mycobacteria smegmatis but also Mycobacteria tuberculosis. M. smegmatis is used as a model for mycobacterial species. It is useful for the research analysis of other...
Reference: AG-CN2-0131-M001
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Specific anti-mycobacterial. Inhibits growth of Mycobacteria smegmatis but also Mycobacteria tuberculosis. M. smegmatis is used as a model for mycobacterial species. It is useful for the research analysis of other...
Reference: AG-CN2-0134-M001
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Antimicrobial. Phytotoxic. Specific acetylcholinesterase (AChE) inhibitor.
Reference: AG-CN2-0134-M005
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Antimicrobial. Phytotoxic. Specific acetylcholinesterase (AChE) inhibitor.
Reference: AG-CN2-0135-M001
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Free radical scavenger and antioxidant. Potential compound to neutralize radioactive and toxic wastes and "heal" soils. Chelates and binds scores of minerals into a bioavailable form used by cells. Shown to...
Reference: AG-CN2-0135-M005
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Free radical scavenger and antioxidant. Potential compound to neutralize radioactive and toxic wastes and "heal" soils. Chelates and binds scores of minerals into a bioavailable form used by cells. Shown to...
Reference: AG-CN2-0136-M001
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Antimicrobial. Phytotoxic.
Reference: AG-CN2-0137-M001
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Matrix metalloproteinase-1 (MMP-1; Type I collagenase) inhibitor. HIV-1 integrase inhibitor.
Reference: AG-CN2-0138-M001
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Mycotoxin. Antibacterial agent. ADP transport inhibitor. Mitochondrial respiration and oxidative phosphorylation inhibitor. Human CCR5 receptor antagonist. Anti-HIV compound.
Reference: AG-CN2-0138-MM25
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Mycotoxin. Antibacterial agent. ADP transport inhibitor. Mitochondrial respiration and oxidative phosphorylation inhibitor. Human CCR5 receptor antagonist. Anti-HIV compound.
Reference: AG-CN2-0139-M001
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Plasminogen activator inhibitor (PAI-1). Glucose uptake stimulator.
Reference: AG-CN2-0139-M005
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Plasminogen activator inhibitor (PAI-1). Glucose uptake stimulator.
Reference: AG-CN2-0140-M001
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Antiprotozoal (Leishmania). Antifungal.
Reference: AG-CN2-0142-C500
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Tremorgenic mycotoxin. Potent and specific, irreversible acetylcholinesterase (AChE) inhibitor.
Reference: AG-CN2-0142-M001
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Tremorgenic mycotoxin. Potent and specific, irreversible acetylcholinesterase (AChE) inhibitor.
Reference: AG-CN2-0144-C250
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Mycotoxin. Protein farnesyltransferase (PFTase) inhibitor. Anti-cancer compound. Directly interacts with P-glycoprotein and inhibits the efflux of antitumor agents in drug resistant cells.
Reference: AG-CN2-0144-M001
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Mycotoxin. Protein farnesyltransferase (PFTase) inhibitor. Anti-cancer compound. Directly interacts with P-glycoprotein and inhibits the efflux of antitumor agents in drug resistant cells.
Reference: AG-CN2-0154-M001
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Antimitotic. Cell cycle inhibitor at the G2/M phase. Antiproliferative. Weak CNS stimulant with weak inhibitory activity on blood platelet aggregation. Mycotoxin.
Reference: AG-CN2-0154-M005
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Antimitotic. Cell cycle inhibitor at the G2/M phase. Antiproliferative. Weak CNS stimulant with weak inhibitory activity on blood platelet aggregation. Mycotoxin.
Reference: AG-CN2-0156-C250
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Antioxidant. Radical scavenging activity towards DPPH and superoxide. Shows a suppressive effect on the expression of vascular cell adhesion molecule-1 (VCAM-1) in human umbilical vein endothelial cells (HUVECs)...
Reference: AG-CN2-0156-M001
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Antioxidant. Radical scavenging activity towards DPPH and superoxide. Shows a suppressive effect on the expression of vascular cell adhesion molecule-1 (VCAM-1) in human umbilical vein endothelial cells (HUVECs)...
Reference: AG-CN2-0163-M001
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Derivative of aszonalenin, a substance P inhibitor.
Reference: AG-CN2-0163-M005
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Derivative of aszonalenin, a substance P inhibitor.
Reference: AG-CN2-0167-M001
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Tremorgenic. Potent, selective and reversible inhibitor of high-conductance calcium-activated potassium (BKCa) channels. Reversible inhibitor of inositol 1,4,5-trisphosphate receptor (InsP(3)). Sarco/endoplasmic...
Reference: AG-CN2-0167-M005
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Tremorgenic. Potent, selective and reversible inhibitor of high-conductance calcium-activated potassium (BKCa) channels. Reversible inhibitor of inositol 1,4,5-trisphosphate receptor (InsP(3)). Sarco/endoplasmic...
Reference: AG-CN2-0168-M001
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Cytotoxic. Melanogenesis inhibitor without cytotoxicity.
Reference: AG-CN2-0168-MM25
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Cytotoxic. Melanogenesis inhibitor without cytotoxicity.
Reference: AG-CN2-0170-C250
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Weak blood platelet aggregation inhibitor compared to Herquline B.
Reference: AG-CN2-0170-M001
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Weak blood platelet aggregation inhibitor compared to Herquline B.
Reference: AG-CN2-0171-C250
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Anticancer compound. Cytotoxic against human breast cancer cells. Induces autophagic cell death in MCF-7 cells. Moderate radical scavenger. Weak acetylcholinesterase (AChE) inhibitor. Shows moderate trypanocidal...
Reference: AG-CN2-0171-M001
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Anticancer compound. Cytotoxic against human breast cancer cells. Induces autophagic cell death in MCF-7 cells. Moderate radical scavenger. Weak acetylcholinesterase (AChE) inhibitor. Shows moderate trypanocidal...
Reference: AG-CN2-0173-C500
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Selective apoptosis inducer in ras-dependent cells. Autophagy (Akt-dependent), apoptosis and necroptosis inducer in renal cancer cell lines. Induces death of ras-mutated pancreatic tumor (Panc-1) cells in vitro and in...
Reference: AG-CN2-0174-C250
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Potent anticancer agent. Inhibits cell growth, proliferation and survival of human tumor cells lines in vivo and in vitro. Exhibits strong cytotoxicity against a panel of human solid tumor cell lines, disrupting the...
Reference: AG-CN2-0174-M001
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Potent anticancer agent. Inhibits cell growth, proliferation and survival of human tumor cells lines in vivo and in vitro. Exhibits strong cytotoxicity against a panel of human solid tumor cell lines, disrupting the...
Reference: AG-CN2-0302-M001
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Broad spectrum antifungal agent compared to sordarin. Shows growth inhibitory activity against pathogenic fungal strains such as Candida albicans, Candida glabrata and Cryptococcus neoformans. Inhibits the protein...
Reference: AG-CN2-0309-M001
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Labionin-containing class III lanthipeptide. Antinociceptive agent. Effective in animal models of nociceptic and inflammatory pain. Does not act through opioid, cannabinoid or descending adrenergic mechanisms. Most...
Reference: AG-CN2-0309-M005
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Labionin-containing class III lanthipeptide. Antinociceptive agent. Effective in animal models of nociceptic and inflammatory pain. Does not act through opioid, cannabinoid or descending adrenergic mechanisms. Most...
Reference: AG-CN2-0400-M005
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Apoptosis inducer. Cell cycle arrest inducer. Anticancer compound Antioxidant. Hepatoprotective. Inhibits TGF-beta/Smad-mediated fibrogenesis. Stimulates wound healing. Anti-diabetic. Glycogen phosphorylase inhibitor....
Reference: AG-CN2-0400-M025
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Apoptosis inducer. Cell cycle arrest inducer. Anticancer compound Antioxidant. Hepatoprotective. Inhibits TGF-beta/Smad-mediated fibrogenesis. Stimulates wound healing. Anti-diabetic. Glycogen phosphorylase inhibitor....
Reference: AG-CN2-0402-M005
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Anti-inflammatory. Antibacterial. Antifungal. Haemolytic agent. Weak phosphodiesterase 4 (PDE4) inhibitor.. Antioxidant.
Reference: AG-CN2-0402-M025
€0.00 (tax incl.)
Anti-inflammatory. Antibacterial. Antifungal. Haemolytic agent. Weak phosphodiesterase 4 (PDE4) inhibitor.. Antioxidant.

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