Reagents (3)

Umbellulone

Reference: AG-CN2-0085-M010

€0.00 (tax incl.)

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...

Piceatannol

Reference: AG-CN2-0086-M001

€0.00 (tax incl.)

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....

Piceatannol

Reference: AG-CN2-0086-M005

€0.00 (tax incl.)

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....

Piceatannol

Reference: AG-CN2-0086-M025

€0.00 (tax incl.)

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....

Apicidin

Reference: AG-CN2-0087-M001

€0.00 (tax incl.)

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...

Apicidin

Reference: AG-CN2-0087-M005

€0.00 (tax incl.)

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...

Forskolin

Reference: AG-CN2-0089-M001

€0.00 (tax incl.)

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....

Forskolin

Reference: AG-CN2-0089-M005

€0.00 (tax incl.)

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....

Forskolin

Reference: AG-CN2-0089-M025

€0.00 (tax incl.)

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....

Forskolin

Reference: AG-CN2-0089-M050

€0.00 (tax incl.)

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....

Xanthorrhizol

Reference: AG-CN2-0090-M001

€0.00 (tax incl.)

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....

Rubratoxin A

Reference: AG-CN2-0092-C250

€0.00 (tax incl.)

Mycotoxin. Potent and selective competitive protein phosphatase 2A (PP2A) inhibitor. Does not inhibit PP1, PP2B, PTP1B, ALP and CIP. Antitumor agent. Antimetastatic.

Rubratoxin A

Reference: AG-CN2-0092-C500

€0.00 (tax incl.)

Mycotoxin. Potent and selective competitive protein phosphatase 2A (PP2A) inhibitor. Does not inhibit PP1, PP2B, PTP1B, ALP and CIP. Antitumor agent. Antimetastatic.

Cytostatin

Reference: AG-CN2-0093-C250

€0.00 (tax incl.)

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....

Luteolin

Reference: AG-CN2-0098-M005

€0.00 (tax incl.)

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)...

Luteolin

Reference: AG-CN2-0098-M025

€0.00 (tax incl.)

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)...

EM574 [Motilide]

Reference: AG-CN2-0102-C250

€0.00 (tax incl.)

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...

EM574 [Motilide]

Reference: AG-CN2-0102-M001

€0.00 (tax incl.)

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...

Lactacystin

Reference: AG-CN2-0104-C100

€0.00 (tax incl.)

Induces neuritogenesis. Potent and selective irreversible proteasome inhibitor. Specifically inhibits 20S proteasome (MCP; multicatalytic complex). Blocks proteasome activity by targeting the catalytic beta-subunit....

Lactacystin

Reference: AG-CN2-0104-C200

€0.00 (tax incl.)

Induces neuritogenesis. Potent and selective irreversible proteasome inhibitor. Specifically inhibits 20S proteasome (MCP; multicatalytic complex). Blocks proteasome activity by targeting the catalytic beta-subunit....

Lactacystin

Reference: AG-CN2-0104-C500

€0.00 (tax incl.)

Induces neuritogenesis. Potent and selective irreversible proteasome inhibitor. Specifically inhibits 20S proteasome (MCP; multicatalytic complex). Blocks proteasome activity by targeting the catalytic beta-subunit....

Lactacystin

Reference: AG-CN2-0104-M001

€0.00 (tax incl.)

Induces neuritogenesis. Potent and selective irreversible proteasome inhibitor. Specifically inhibits 20S proteasome (MCP; multicatalytic complex). Blocks proteasome activity by targeting the catalytic beta-subunit....

Amidepsine A

Reference: AG-CN2-0109-M001

€0.00 (tax incl.)

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...

Amidepsine A

Reference: AG-CN2-0109-MM25

€0.00 (tax incl.)

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...

Amidepsine D

Reference: AG-CN2-0110-M001

€0.00 (tax incl.)

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...

Amidepsine D

Reference: AG-CN2-0110-MM25

€0.00 (tax incl.)

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...

Cercosporin

Reference: AG-CN2-0111-M001

€0.00 (tax incl.)

Phytotoxin. Potent and specific PKC inhibitor. Competes for the phorbol binding site. Anticancer compound. Cytotoxic. Antiproliferative. Antiparasitic. Antimicrobial.

Cercosporin

Reference: AG-CN2-0111-M005

€0.00 (tax incl.)

Phytotoxin. Potent and specific PKC inhibitor. Competes for the phorbol binding site. Anticancer compound. Cytotoxic. Antiproliferative. Antiparasitic. Antimicrobial.

Dihydrochlamydocin

Reference: AG-CN2-0115-C250

€0.00 (tax incl.)

Phytotoxin. Derivative of HDAC inhibitor chlamydocin Similar chemical structure to the TAN-1746 compounds (potent HDAC inhibitors).

Dihydrochlamydocin

Reference: AG-CN2-0115-M001

€0.00 (tax incl.)

Phytotoxin. Derivative of HDAC inhibitor chlamydocin Similar chemical structure to the TAN-1746 compounds (potent HDAC inhibitors).

Harzianum A

Reference: AG-CN2-0117-C250

€0.00 (tax incl.)

Antifungal. Anticancer compound. Cytotoxic to human cancer cell lines.

Harzianum A

Reference: AG-CN2-0117-M001

€0.00 (tax incl.)

Antifungal. Anticancer compound. Cytotoxic to human cancer cell lines.

17-Hydroxyventuricidin A

Reference: AG-CN2-0119-C250

€0.00 (tax incl.)

Antifungal. Antibacterial against Gram-positive bacteria.

17-Hydroxyventuricidin A

Reference: AG-CN2-0119-M001

€0.00 (tax incl.)

Antifungal. Antibacterial against Gram-positive bacteria.

Lariatin A

Reference: AG-CN2-0120-C250

€0.00 (tax incl.)

Peptide with lasso structure. Antimycobacterial.

Lariatin A

Reference: AG-CN2-0120-M001

€0.00 (tax incl.)

Peptide with lasso structure. Antimycobacterial.

11-O-Methylpseurotin A

Reference: AG-CN2-0121-C250

€0.00 (tax incl.)

Antibacterial. Selectively inhibits a Hof1 deletion strain.

11-O-Methylpseurotin A

Reference: AG-CN2-0121-M001

€0.00 (tax incl.)

Antibacterial. Selectively inhibits a Hof1 deletion strain.

Penicillide

Reference: AG-CN2-0122-C250

€0.00 (tax incl.)

Plant growth inhibitor. Acyl-CoA-cholesterol acyltransferase (ACAT) inhibitor. Anticancer compound. Cytotoxic. Non-peptidic oxytocin receptor antagonist. Calpain inhibitor.

Penicillide

Reference: AG-CN2-0122-M001

€0.00 (tax incl.)

Plant growth inhibitor. Acyl-CoA-cholesterol acyltransferase (ACAT) inhibitor. Anticancer compound. Cytotoxic. Non-peptidic oxytocin receptor antagonist. Calpain inhibitor.

Terpendole C

Reference: AG-CN2-0125-C250

€0.00 (tax incl.)

Acyl-CoA:cholesterol acyltransferase (ACAT) isozymes ACAT1 and ACAT2 inhibitor. Tremorgenic. Cholesteryl ester (CE) synthesis inhibitor.

Terpendole C

Reference: AG-CN2-0125-M001

€0.00 (tax incl.)

Acyl-CoA:cholesterol acyltransferase (ACAT) isozymes ACAT1 and ACAT2 inhibitor. Tremorgenic. Cholesteryl ester (CE) synthesis inhibitor.

Terpendole E

Reference: AG-CN2-0127-C250

€0.00 (tax incl.)

Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. Mitotic kinesin Eg5 (Mitotic Kinesin Spindle Protein; KSP) inhibitor. Specific M phase inhibitor.

Calpinactam

Reference: AG-CN2-0131-C250

€0.00 (tax incl.)

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...

Calpinactam

Reference: AG-CN2-0131-M001

€0.00 (tax incl.)

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...

Cyclopenin

Reference: AG-CN2-0134-M001

€0.00 (tax incl.)

Antimicrobial. Phytotoxic. Specific acetylcholinesterase (AChE) inhibitor.

Cyclopenin

Reference: AG-CN2-0134-M005

€0.00 (tax incl.)

Antimicrobial. Phytotoxic. Specific acetylcholinesterase (AChE) inhibitor.

Fulvic acid

Reference: AG-CN2-0135-M001

€0.00 (tax incl.)

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...

Fulvic acid

Reference: AG-CN2-0135-M005

€0.00 (tax incl.)

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...

Cyclopenol

Reference: AG-CN2-0136-M001

€0.00 (tax incl.)

Antimicrobial. Phytotoxic.

Funalenone

Reference: AG-CN2-0137-M001

€0.00 (tax incl.)

Matrix metalloproteinase-1 (MMP-1; Type I collagenase) inhibitor. HIV-1 integrase inhibitor.

Fuscin

Reference: AG-CN2-0138-M001

€0.00 (tax incl.)

Mycotoxin. Antibacterial agent. ADP transport inhibitor. Mitochondrial respiration and oxidative phosphorylation inhibitor. Human CCR5 receptor antagonist. Anti-HIV compound.

Fuscin

Reference: AG-CN2-0138-MM25

€0.00 (tax incl.)

Mycotoxin. Antibacterial agent. ADP transport inhibitor. Mitochondrial respiration and oxidative phosphorylation inhibitor. Human CCR5 receptor antagonist. Anti-HIV compound.

Geodin

Reference: AG-CN2-0139-M001

€0.00 (tax incl.)

Plasminogen activator inhibitor (PAI-1). Glucose uptake stimulator.

Geodin

Reference: AG-CN2-0139-M005

€0.00 (tax incl.)

Plasminogen activator inhibitor (PAI-1). Glucose uptake stimulator.

Palitantin

Reference: AG-CN2-0140-M001

€0.00 (tax incl.)

Antiprotozoal (Leishmania). Antifungal.

Territrem B

Reference: AG-CN2-0142-C500

€0.00 (tax incl.)

Tremorgenic mycotoxin. Potent and specific, irreversible acetylcholinesterase (AChE) inhibitor.

Territrem B

Reference: AG-CN2-0142-M001

€0.00 (tax incl.)

Tremorgenic mycotoxin. Potent and specific, irreversible acetylcholinesterase (AChE) inhibitor.

Andrastin A

Reference: AG-CN2-0144-C250

€0.00 (tax incl.)

Mycotoxin. Protein farnesyltransferase (PFTase) inhibitor. Anti-cancer compound. Directly interacts with P-glycoprotein and inhibits the efflux of antitumor agents in drug resistant cells.

Andrastin A

Reference: AG-CN2-0144-M001

€0.00 (tax incl.)

Mycotoxin. Protein farnesyltransferase (PFTase) inhibitor. Anti-cancer compound. Directly interacts with P-glycoprotein and inhibits the efflux of antitumor agents in drug resistant cells.

Neoxaline

Reference: AG-CN2-0154-M001

€0.00 (tax incl.)

Antimitotic. Cell cycle inhibitor at the G2/M phase. Antiproliferative. Weak CNS stimulant with weak inhibitory activity on blood platelet aggregation. Mycotoxin.

Neoxaline

Reference: AG-CN2-0154-M005

€0.00 (tax incl.)

Antimitotic. Cell cycle inhibitor at the G2/M phase. Antiproliferative. Weak CNS stimulant with weak inhibitory activity on blood platelet aggregation. Mycotoxin.

Pyranonigrin A

Reference: AG-CN2-0156-C250

€0.00 (tax incl.)

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)...

Pyranonigrin A

Reference: AG-CN2-0156-M001

€0.00 (tax incl.)

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)...

epi-Aszonalenin A

Reference: AG-CN2-0163-M001

€0.00 (tax incl.)

Derivative of aszonalenin, a substance P inhibitor.

epi-Aszonalenin A

Reference: AG-CN2-0163-M005

€0.00 (tax incl.)

Derivative of aszonalenin, a substance P inhibitor.

Paxilline

Reference: AG-CN2-0167-M001

€0.00 (tax incl.)

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...

Paxilline

Reference: AG-CN2-0167-M005

€0.00 (tax incl.)

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...

Aspochalasin I

Reference: AG-CN2-0168-M001

€0.00 (tax incl.)

Cytotoxic. Melanogenesis inhibitor without cytotoxicity.

Aspochalasin I

Reference: AG-CN2-0168-MM25

€0.00 (tax incl.)

Cytotoxic. Melanogenesis inhibitor without cytotoxicity.

Herquline A

Reference: AG-CN2-0170-C250

€0.00 (tax incl.)

Weak blood platelet aggregation inhibitor compared to Herquline B.

Herquline A

Reference: AG-CN2-0170-M001

€0.00 (tax incl.)

Weak blood platelet aggregation inhibitor compared to Herquline B.

Asperphenamate

Reference: AG-CN2-0171-C250

€0.00 (tax incl.)

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...

Asperphenamate

Reference: AG-CN2-0171-M001

€0.00 (tax incl.)

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...

Rasfonin

Reference: AG-CN2-0173-C500

€0.00 (tax incl.)

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...

Globosuxanthone A

Reference: AG-CN2-0174-C250

€0.00 (tax incl.)

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...

Globosuxanthone A

Reference: AG-CN2-0174-M001

€0.00 (tax incl.)

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...

BE-31405

Reference: AG-CN2-0302-M001

€0.00 (tax incl.)

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...

NAI-112

Reference: AG-CN2-0309-M001

€0.00 (tax incl.)

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...

NAI-112

Reference: AG-CN2-0309-M005

€0.00 (tax incl.)

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...

Asiatic acid

Reference: AG-CN2-0400-M005

€0.00 (tax incl.)

Apoptosis inducer. Cell cycle arrest inducer. Anticancer compound Antioxidant. Hepatoprotective. Inhibits TGF-beta/Smad-mediated fibrogenesis. Stimulates wound healing. Anti-diabetic. Glycogen phosphorylase inhibitor....

Asiatic acid

Reference: AG-CN2-0400-M025

€0.00 (tax incl.)

Apoptosis inducer. Cell cycle arrest inducer. Anticancer compound Antioxidant. Hepatoprotective. Inhibits TGF-beta/Smad-mediated fibrogenesis. Stimulates wound healing. Anti-diabetic. Glycogen phosphorylase inhibitor....

Sericic acid

Reference: AG-CN2-0402-M005

€0.00 (tax incl.)

Anti-inflammatory. Antibacterial. Antifungal. Haemolytic agent. Weak phosphodiesterase 4 (PDE4) inhibitor.. Antioxidant.

Sericic acid

Reference: AG-CN2-0402-M025

€0.00 (tax incl.)

Anti-inflammatory. Antibacterial. Antifungal. Haemolytic agent. Weak phosphodiesterase 4 (PDE4) inhibitor.. Antioxidant.

Ledol

Reference: AG-CN2-0406-M500

€0.00 (tax incl.)

Toxic sesquiterpenoid. Exhibits expectorant and antitussive effect. Reported to increase blood pressure. Antifungal compound.

Ledol

Reference: AG-CN2-0406-G001

€0.00 (tax incl.)

Toxic sesquiterpenoid. Exhibits expectorant and antitussive effect. Reported to increase blood pressure. Antifungal compound.

(+)-Catechin . hydrate

Reference: AG-CN2-0407-M500

€0.00 (tax incl.)

Specific histidine decarboxylase inhibitor. Anti-inflammatory. COX-1 inhibitor. Antioxidant flavonoid. Free radical scavenger. Inhibits lipid peroxidation. Antimetastatic and anticancer compound. Antiangiogenic....

(+)-Catechin . hydrate

Reference: AG-CN2-0407-G001

€0.00 (tax incl.)

Specific histidine decarboxylase inhibitor. Anti-inflammatory. COX-1 inhibitor. Antioxidant flavonoid. Free radical scavenger. Inhibits lipid peroxidation. Antimetastatic and anticancer compound. Antiangiogenic....

Rutin . trihydrate

Reference: AG-CN2-0408-G005

€0.00 (tax incl.)

Antioxidant. Free radical scavenger. Nitric oxide (NO) scavenger. Anticancer compound. Antiproliferative. Apoptosis inducer. Reduces induced DNA damage. Protective against carcinogenesis. Hypolipidaemic. Reduces...

Quercetin . dihydrate

Reference: AG-CN2-0409-G001

€0.00 (tax incl.)

Multipotent flavonoid antioxidant. Potent free radical scavenger. Neuroprotective. Anticancer compound with chemosensitizing activity. Cell cycle arrest, apoptosis and autophagy inducer. Proteasome inhibitor....

Quercetin . dihydrate

Reference: AG-CN2-0409-G005

€0.00 (tax incl.)

Multipotent flavonoid antioxidant. Potent free radical scavenger. Neuroprotective. Anticancer compound with chemosensitizing activity. Cell cycle arrest, apoptosis and autophagy inducer. Proteasome inhibitor....

Chenodeoxycholic acid

Reference: AG-CN2-0410-M100

€0.00 (tax incl.)

Cytotoxic hydrophobic primary bile acid. Activator of farnesoid X receptor (FXR), a nuclear receptor that is hepatoprotective and regulates bile acid synthesis (cholesterol 7alpha-hydroxylase (CYP7A1) suppression),...

Chenodeoxycholic acid

Reference: AG-CN2-0410-M500

€0.00 (tax incl.)

Cytotoxic hydrophobic primary bile acid. Activator of farnesoid X receptor (FXR), a nuclear receptor that is hepatoprotective and regulates bile acid synthesis (cholesterol 7alpha-hydroxylase (CYP7A1) suppression),...

Ursodeoxycholic acid

Reference: AG-CN2-0411-G001

€0.00 (tax incl.)

Endogenous hydrophilic bile acid. Antioxidant. Cytoprotective against oxidative stress and cell death. Hepatoprotective at cellular and molecular level, including stabilization of membranes. Protects hepatocytes...

Ursodeoxycholic acid

Reference: AG-CN2-0411-G005

€0.00 (tax incl.)

Endogenous hydrophilic bile acid. Antioxidant. Cytoprotective against oxidative stress and cell death. Hepatoprotective at cellular and molecular level, including stabilization of membranes. Protects hepatocytes...

Stigmasterol

Reference: AG-CN2-0412-G001

€0.00 (tax incl.)

Anti-hypercholestrolemic compound. Anti-inflammatory and immune-modulating effects. Anticancer compound. Chemopreventive. Cytostatic. Cell growth inhibitor. Antimutagenic. Potent in vitro antagonist of FXR (farnesoid...

Stigmasterol

Reference: AG-CN2-0412-G005

€0.00 (tax incl.)

Anti-hypercholestrolemic compound. Anti-inflammatory and immune-modulating effects. Anticancer compound. Chemopreventive. Cytostatic. Cell growth inhibitor. Antimutagenic. Potent in vitro antagonist of FXR (farnesoid...

Meglumine

Reference: AG-CN2-0413-G001

€0.00 (tax incl.)

Used as an excipient (an inert substance) in pharmaceuticals that improves solubility, drug release rate and stabilization of anionic drug substances. Counter ion used to replace sodium. It is impermeable towards cell...

Meglumine

Reference: AG-CN2-0413-G005

€0.00 (tax incl.)

Used as an excipient (an inert substance) in pharmaceuticals that improves solubility, drug release rate and stabilization of anionic drug substances. Counter ion used to replace sodium. It is impermeable towards cell...

Papaverine . hydrochloride

Reference: AG-CN2-0414-G001

€0.00 (tax incl.)

Smooth muscle relaxant and vasodilator. Phosphodiesterase PDE10A inhibitor. Antiviral. Antipsychotic. Potential inducer of browning in WAT.

Category: Reagents

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