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(+)-15-epi Cloprostenol (+)-15-epi Cloprostenol

(+)-15-epi Cloprostenol

Reference: 10006692-500
€0.00 (tax incl.)
Cloprostenol is a synthetic PGF2α analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude...
(+)-15-epi Cloprostenol (+)-15-epi Cloprostenol

(+)-15-epi Cloprostenol

Reference: 10006692-5
€0.00 (tax incl.)
Cloprostenol is a synthetic PGF2α analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude...
(+)-15-epi Cloprostenol (+)-15-epi Cloprostenol

(+)-15-epi Cloprostenol

Reference: 10006692-10
€0.00 (tax incl.)
Cloprostenol is a synthetic PGF2α analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude...
(+)-15-epi Cloprostenol (+)-15-epi Cloprostenol

(+)-15-epi Cloprostenol

Reference: 10006692-1
€0.00 (tax incl.)
Cloprostenol is a synthetic PGF2α analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol is the 15(S), or 15β-hydroxy enantiomer of (+)-cloprostenol. This epimer is less active by several orders of magnitude...
(+)-2,5-epi Goniothalesdiol (+)-2,5-epi Goniothalesdiol

(+)-2,5-epi Goniothalesdiol

Reference: 10008887-5
€0.00 (tax incl.)
An analog of goniothalesdiol, a tetrahydrofuran compound known to have significant cytotoxic effects against P388 murine leukemia cells and pesticidal activities.
(+)-2,5-epi Goniothalesdiol (+)-2,5-epi Goniothalesdiol

(+)-2,5-epi Goniothalesdiol

Reference: 10008887-10
€0.00 (tax incl.)
An analog of goniothalesdiol, a tetrahydrofuran compound known to have significant cytotoxic effects against P388 murine leukemia cells and pesticidal activities.
(+)-2,5-epi Goniothalesdiol (+)-2,5-epi Goniothalesdiol

(+)-2,5-epi Goniothalesdiol

Reference: 10008887-1
€0.00 (tax incl.)
An analog of goniothalesdiol, a tetrahydrofuran compound known to have significant cytotoxic effects against P388 murine leukemia cells and pesticidal activities.
(+)-3-Carene (+)-3-Carene

(+)-3-Carene

Reference: 23165-100
€0.00 (tax incl.)
A monoterpene; a component of (±)-3-carene
(+)-5-trans Cloprostenol (+)-5-trans Cloprostenol

(+)-5-trans Cloprostenol

Reference: 10004970-5
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
(+)-5-trans Cloprostenol (+)-5-trans Cloprostenol

(+)-5-trans Cloprostenol

Reference: 10004970-25
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
(+)-5-trans Cloprostenol (+)-5-trans Cloprostenol

(+)-5-trans Cloprostenol

Reference: 10004970-10
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
(+)-5-trans Cloprostenol (+)-5-trans Cloprostenol

(+)-5-trans Cloprostenol

Reference: 10004970-1
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
(+)-Abscisic Acid (+)-Abscisic Acid

(+)-Abscisic Acid

Reference: 10073-50
€0.00 (tax incl.)
A plant hormone with diverse roles in disease resistance, plant development, and response to stresses; regulates gene expression and may contribute to epigenetic changes at the chromatin level
(+)-Abscisic Acid (+)-Abscisic Acid

(+)-Abscisic Acid

Reference: 10073-5
€0.00 (tax incl.)
A plant hormone with diverse roles in disease resistance, plant development, and response to stresses; regulates gene expression and may contribute to epigenetic changes at the chromatin level
(+)-Abscisic Acid (+)-Abscisic Acid

(+)-Abscisic Acid

Reference: 10073-10
€0.00 (tax incl.)
A plant hormone with diverse roles in disease resistance, plant development, and response to stresses; regulates gene expression and may contribute to epigenetic changes at the chromatin level
(+)-Abscisic Acid (+)-Abscisic Acid

(+)-Abscisic Acid

Reference: 10073-1
€0.00 (tax incl.)
A plant hormone with diverse roles in disease resistance, plant development, and response to stresses; regulates gene expression and may contribute to epigenetic changes at the chromatin level
(+)-Abscisic Acid-d6 (+)-Abscisic Acid-d6

(+)-Abscisic Acid-d6

Reference: 29093-1
€0.00 (tax incl.)
An internal standard for the quantification of (+)-abscisic acid by GC- or LC-MS
(+)-Aeroplysinin-1 (+)-Aeroplysinin-1

(+)-Aeroplysinin-1

Reference: 21498-100
€0.00 (tax incl.)
A sea sponge metabolite with diverse biological activities; induces cell death in MCF-7 and ZR-75-1 human breast cancer cells in a time- and concentration-dependent manner from 0.25-0.5 μM; blocks EGF-induced...
(+)-Alliin (+)-Alliin

(+)-Alliin

Reference: 14002-5
€0.00 (tax incl.)
A cysteine sulfoxide constituent of garlic that exhibits anti-cancer, anti-microbial, anti-hypertensive, cardioprotective, and anti-oxidant activities; S-allyl-cysteine is oxidized stereospecifically to (+)-alliin by...
(+)-Alliin (+)-Alliin

(+)-Alliin

Reference: 14002-10
€0.00 (tax incl.)
A cysteine sulfoxide constituent of garlic that exhibits anti-cancer, anti-microbial, anti-hypertensive, cardioprotective, and anti-oxidant activities; S-allyl-cysteine is oxidized stereospecifically to (+)-alliin by...
(+)-Alliin (+)-Alliin

(+)-Alliin

Reference: 14002-1
€0.00 (tax incl.)
A cysteine sulfoxide constituent of garlic that exhibits anti-cancer, anti-microbial, anti-hypertensive, cardioprotective, and anti-oxidant activities; S-allyl-cysteine is oxidized stereospecifically to (+)-alliin by...
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: 14007-5
€0.00 (tax incl.)
A natural tetracyclic diterpene with antiviral activity against herpes simplex; a cell-permeable, reversible inhibitor of DNA replication in eukaryotic cells, specifically blocking the activity of DNA polymerases α,...
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: 14007-25
€0.00 (tax incl.)
A natural tetracyclic diterpene with antiviral activity against herpes simplex; a cell-permeable, reversible inhibitor of DNA replication in eukaryotic cells, specifically blocking the activity of DNA polymerases α,...
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: 14007-1
€0.00 (tax incl.)
A natural tetracyclic diterpene with antiviral activity against herpes simplex; a cell-permeable, reversible inhibitor of DNA replication in eukaryotic cells, specifically blocking the activity of DNA polymerases α,...
(+)-ar-Turmerone (+)-ar-Turmerone

(+)-ar-Turmerone

Reference: 11759-5
€0.00 (tax incl.)
An aromatic compound that stimulates the proliferation of peripheral blood mononuclear cells and increases the production of TNF-α, IL-2, and IFN-γ; promotes the maturation of dendritic cells and induces the...
(+)-ar-Turmerone (+)-ar-Turmerone

(+)-ar-Turmerone

Reference: 11759-10
€0.00 (tax incl.)
An aromatic compound that stimulates the proliferation of peripheral blood mononuclear cells and increases the production of TNF-α, IL-2, and IFN-γ; promotes the maturation of dendritic cells and induces the...
(+)-ar-Turmerone (+)-ar-Turmerone

(+)-ar-Turmerone

Reference: 11759-1
€0.00 (tax incl.)
An aromatic compound that stimulates the proliferation of peripheral blood mononuclear cells and increases the production of TNF-α, IL-2, and IFN-γ; promotes the maturation of dendritic cells and induces the...
(+)-AS 115 (+)-AS 115

(+)-AS 115

Reference: 10009650-500
€0.00 (tax incl.)
A single enantiomer of a potent and selective inactivator of KIAA1363, a MAGE hydrolase an enzyme that is upregulated in aggressive cancers from various tissues (IC50 = 150 nM when tested as a racemic mixture in...
(+)-AS 115 (+)-AS 115

(+)-AS 115

Reference: 10009650-100
€0.00 (tax incl.)
A single enantiomer of a potent and selective inactivator of KIAA1363, a MAGE hydrolase an enzyme that is upregulated in aggressive cancers from various tissues (IC50 = 150 nM when tested as a racemic mixture in...
(+)-AS 115 (+)-AS 115

(+)-AS 115

Reference: 10009650-1
€0.00 (tax incl.)
A single enantiomer of a potent and selective inactivator of KIAA1363, a MAGE hydrolase an enzyme that is upregulated in aggressive cancers from various tissues (IC50 = 150 nM when tested as a racemic mixture in...
(+)-Atenolol (+)-Atenolol

(+)-Atenolol

Reference: 18623-5
€0.00 (tax incl.)
An enantiomer of (±)-atenolol; inhibits radioligand binding to β-ARs on sarcolemma-enriched membranes (Ki = 8.61 µM); has no effect on blood pressure in spontaneously hypertensive rats
(+)-Atenolol (+)-Atenolol

(+)-Atenolol

Reference: 18623-25
€0.00 (tax incl.)
An enantiomer of (±)-atenolol; inhibits radioligand binding to β-ARs on sarcolemma-enriched membranes (Ki = 8.61 µM); has no effect on blood pressure in spontaneously hypertensive rats
(+)-Atenolol (+)-Atenolol

(+)-Atenolol

Reference: 18623-10
€0.00 (tax incl.)
An enantiomer of (±)-atenolol; inhibits radioligand binding to β-ARs on sarcolemma-enriched membranes (Ki = 8.61 µM); has no effect on blood pressure in spontaneously hypertensive rats
(+)-Atenolol (+)-Atenolol

(+)-Atenolol

Reference: 18623-1
€0.00 (tax incl.)
An enantiomer of (±)-atenolol; inhibits radioligand binding to β-ARs on sarcolemma-enriched membranes (Ki = 8.61 µM); has no effect on blood pressure in spontaneously hypertensive rats
(+)-Baclofen (hydrochloride) (+)-Baclofen (hydrochloride)

(+)-Baclofen (hydrochloride)

Reference: 31595-50
€0.00 (tax incl.)
A GABAB receptor agonist; increases latency to paw or tail withdrawal in the hot-plate test in mice at 1 and 3 mg/kg; reduces the number of lever responses for alcohol in Sardinian alcohol-preferring rats at 3 mg/kg
(+)-Baclofen (hydrochloride) (+)-Baclofen (hydrochloride)

(+)-Baclofen (hydrochloride)

Reference: 31595-25
€0.00 (tax incl.)
A GABAB receptor agonist; increases latency to paw or tail withdrawal in the hot-plate test in mice at 1 and 3 mg/kg; reduces the number of lever responses for alcohol in Sardinian alcohol-preferring rats at 3 mg/kg
(+)-Baclofen (hydrochloride) (+)-Baclofen (hydrochloride)

(+)-Baclofen (hydrochloride)

Reference: 31595-10
€0.00 (tax incl.)
A GABAB receptor agonist; increases latency to paw or tail withdrawal in the hot-plate test in mice at 1 and 3 mg/kg; reduces the number of lever responses for alcohol in Sardinian alcohol-preferring rats at 3 mg/kg
(+)-Blebbistatin (+)-Blebbistatin

(+)-Blebbistatin

Reference: 13165-5
€0.00 (tax incl.)
An inactive enantiomer of (–)-blebbistatin; (R)-nitro-blebbistatin is a more stable form of (+)-blebbistatin,
(+)-Blebbistatin (+)-Blebbistatin

(+)-Blebbistatin

Reference: 13165-25
€0.00 (tax incl.)
An inactive enantiomer of (–)-blebbistatin; (R)-nitro-blebbistatin is a more stable form of (+)-blebbistatin,
(+)-Blebbistatin (+)-Blebbistatin

(+)-Blebbistatin

Reference: 13165-10
€0.00 (tax incl.)
An inactive enantiomer of (–)-blebbistatin; (R)-nitro-blebbistatin is a more stable form of (+)-blebbistatin,
(+)-Blebbistatin (+)-Blebbistatin

(+)-Blebbistatin

Reference: 13165-1
€0.00 (tax incl.)
An inactive enantiomer of (–)-blebbistatin; (R)-nitro-blebbistatin is a more stable form of (+)-blebbistatin,
(+)-Borneol (+)-Borneol

(+)-Borneol

Reference: 23467-500
€0.00 (tax incl.)
A bicyclic monoterpene with diverse biological activities; a positive allosteric modulator of α1β2γ2L subunit-containing GABAA receptors (EC50 = 248 μM for human recombinant receptors); dose-dependently increases the...
(+)-Borneol (+)-Borneol

(+)-Borneol

Reference: 23467-1
€0.00 (tax incl.)
A bicyclic monoterpene with diverse biological activities; a positive allosteric modulator of α1β2γ2L subunit-containing GABAA receptors (EC50 = 248 μM for human recombinant receptors); dose-dependently increases the...
(+)-Catechin (hydrate) (+)-Catechin (hydrate)

(+)-Catechin (hydrate)

Reference: 70940-5
€0.00 (tax incl.)
Catechin is a polyphenolic flavonoid which has been isolated from a variety of natural sources including tea leaves, grape seeds, and the wood and bark of trees such as acacia and mahogany. Catechin is a more potent...
(+)-Catechin (hydrate) (+)-Catechin (hydrate)

(+)-Catechin (hydrate)

Reference: 70940-25
€0.00 (tax incl.)
Catechin is a polyphenolic flavonoid which has been isolated from a variety of natural sources including tea leaves, grape seeds, and the wood and bark of trees such as acacia and mahogany. Catechin is a more potent...
(+)-Catechin (hydrate) (+)-Catechin (hydrate)

(+)-Catechin (hydrate)

Reference: 70940-10
€0.00 (tax incl.)
Catechin is a polyphenolic flavonoid which has been isolated from a variety of natural sources including tea leaves, grape seeds, and the wood and bark of trees such as acacia and mahogany. Catechin is a more potent...
(+)-Catechin (hydrate) (+)-Catechin (hydrate)

(+)-Catechin (hydrate)

Reference: 70940-1
€0.00 (tax incl.)
Catechin is a polyphenolic flavonoid which has been isolated from a variety of natural sources including tea leaves, grape seeds, and the wood and bark of trees such as acacia and mahogany. Catechin is a more potent...
(+)-Cedrol (+)-Cedrol

(+)-Cedrol

Reference: 25769-250
€0.00 (tax incl.)
A sesquiterpene alcohol; inhibits the growth of L. sulphureus, G. trabeum, L. betulina, and T. versicolor wood decay fungi at 100 μg/ml; inhibits CYP2B6 and CYP3A4 (Kis = 0.9 and 3.4 μM, respectively); prevents hair...
(+)-Cedrol (+)-Cedrol

(+)-Cedrol

Reference: 25769-100
€0.00 (tax incl.)
A sesquiterpene alcohol; inhibits the growth of L. sulphureus, G. trabeum, L. betulina, and T. versicolor wood decay fungi at 100 μg/ml; inhibits CYP2B6 and CYP3A4 (Kis = 0.9 and 3.4 μM, respectively); prevents hair...
(+)-Cloprostenol (+)-Cloprostenol

(+)-Cloprostenol

Reference: 16765-5
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity
(+)-Cloprostenol (+)-Cloprostenol

(+)-Cloprostenol

Reference: 16765-10
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity
(+)-Cloprostenol (+)-Cloprostenol

(+)-Cloprostenol

Reference: 16765-1
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity
(+)-Cloprostenol (sodium salt) (+)-Cloprostenol (sodium salt)

(+)-Cloprostenol (sodium salt)

Reference: 16766-5
€0.00 (tax incl.)
(+)-Cloprostenol (sodium salt) is a more water soluble, crystalline form of (+)-cloprostenol.
(+)-Cloprostenol (sodium salt) (+)-Cloprostenol (sodium salt)

(+)-Cloprostenol (sodium salt)

Reference: 16766-10
€0.00 (tax incl.)
(+)-Cloprostenol (sodium salt) is a more water soluble, crystalline form of (+)-cloprostenol.
(+)-Cloprostenol (sodium salt) (+)-Cloprostenol (sodium salt)

(+)-Cloprostenol (sodium salt)

Reference: 16766-1
€0.00 (tax incl.)
(+)-Cloprostenol (sodium salt) is a more water soluble, crystalline form of (+)-cloprostenol.
(+)-Cloprostenol isopropyl ester (+)-Cloprostenol isopropyl ester

(+)-Cloprostenol isopropyl ester

Reference: 10010016-5
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity; a...
(+)-Cloprostenol isopropyl ester (+)-Cloprostenol isopropyl ester

(+)-Cloprostenol isopropyl ester

Reference: 10010016-10
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity; a...
(+)-Cloprostenol isopropyl ester (+)-Cloprostenol isopropyl ester

(+)-Cloprostenol isopropyl ester

Reference: 10010016-1
€0.00 (tax incl.)
A synthetic analog of PGF2α; an FP receptor agonist and a potent luteolytic agent in rats and hamsters; the optically active, 15(R) enantiomer of cloprostenol responsible for the majority of its biological activity; a...
(+)-Cloprostenol methyl amide (+)-Cloprostenol methyl amide

(+)-Cloprostenol methyl amide

Reference: 10010495-5
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, possibly serving as a prodrug for the bioactive free acid
(+)-Cloprostenol methyl amide (+)-Cloprostenol methyl amide

(+)-Cloprostenol methyl amide

Reference: 10010495-10
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, possibly serving as a prodrug for the bioactive free acid
(+)-Cloprostenol methyl amide (+)-Cloprostenol methyl amide

(+)-Cloprostenol methyl amide

Reference: 10010495-1
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, possibly serving as a prodrug for the bioactive free acid
(+)-Cloprostenol methyl ester (+)-Cloprostenol methyl ester

(+)-Cloprostenol methyl ester

Reference: 10010115-5
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, amenable for certain formulations
(+)-Cloprostenol methyl ester (+)-Cloprostenol methyl ester

(+)-Cloprostenol methyl ester

Reference: 10010115-10
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, amenable for certain formulations
(+)-Cloprostenol methyl ester (+)-Cloprostenol methyl ester

(+)-Cloprostenol methyl ester

Reference: 10010115-1
€0.00 (tax incl.)
A more lipid soluble form of (+)-cloprostenol, amenable for certain formulations
(+)-CP 101,606 (+)-CP 101,606

(+)-CP 101,606

Reference: 23884-5
€0.00 (tax incl.)
An antagonist of NR2B subunit-containing NDMA receptors (Kd = 4.2 nM); selective for NR1/NR2B-containing NMDA receptors over NR1, NR2A, and NR2B subunits alone and NR1/NR2A receptors in HEK293 cell homogenates;...
(+)-CP 101,606 (+)-CP 101,606

(+)-CP 101,606

Reference: 23884-25
€0.00 (tax incl.)
An antagonist of NR2B subunit-containing NDMA receptors (Kd = 4.2 nM); selective for NR1/NR2B-containing NMDA receptors over NR1, NR2A, and NR2B subunits alone and NR1/NR2A receptors in HEK293 cell homogenates;...
(+)-CP 101,606 (+)-CP 101,606

(+)-CP 101,606

Reference: 23884-10
€0.00 (tax incl.)
An antagonist of NR2B subunit-containing NDMA receptors (Kd = 4.2 nM); selective for NR1/NR2B-containing NMDA receptors over NR1, NR2A, and NR2B subunits alone and NR1/NR2A receptors in HEK293 cell homogenates;...
(+)-D-threo-PDMP (hydrochloride) (+)-D-threo-PDMP (hydrochloride)

(+)-D-threo-PDMP (hydrochloride)

Reference: 10178-10
€0.00 (tax incl.)
A glucosylceramide synthase inhibitor; inhibits glucosylceramide synthase by 50% at a 5 µM in an enzyme assay; the active component of racemic DL-threo-PDMP; inhibits the synthesis of glucosylceramide synthase and...
(+)-delta-Tocopherol (+)-delta-Tocopherol

(+)-delta-Tocopherol

Reference: M1790-1
€0.00 (tax incl.)
delta-Tocopherol is one of the forms of vitamin E and in animal tissues has been found to have much less retention than alpha-tocopherol.1 Due to its having only one methyl group meta to the phenolic hydroxyl group...
(+)-Epoxysuberosin (+)-Epoxysuberosin

(+)-Epoxysuberosin

Reference: 30042-5
€0.00 (tax incl.)
A coumarin; has been found in C. album
(+)-Epoxysuberosin (+)-Epoxysuberosin

(+)-Epoxysuberosin

Reference: 30042-1
€0.00 (tax incl.)
A coumarin; has been found in C. album
(+)-Etomoxir (sodium salt) (+)-Etomoxir (sodium salt)

(+)-Etomoxir (sodium salt)

Reference: 11969-50
€0.00 (tax incl.)
An inhibitor of CPT1; inhibits fatty acid transport into the mitochondria for β-oxidation; inhibits fatty acid oxidation in hepatocytes in vitro (IC50s = 0.1, 1, and 10 µM for human, guinea pig, and rat hepatocytes,...
(+)-Etomoxir (sodium salt) (+)-Etomoxir (sodium salt)

(+)-Etomoxir (sodium salt)

Reference: 11969-5
€0.00 (tax incl.)
An inhibitor of CPT1; inhibits fatty acid transport into the mitochondria for β-oxidation; inhibits fatty acid oxidation in hepatocytes in vitro (IC50s = 0.1, 1, and 10 µM for human, guinea pig, and rat hepatocytes,...
(+)-Etomoxir (sodium salt) (+)-Etomoxir (sodium salt)

(+)-Etomoxir (sodium salt)

Reference: 11969-25
€0.00 (tax incl.)
An inhibitor of CPT1; inhibits fatty acid transport into the mitochondria for β-oxidation; inhibits fatty acid oxidation in hepatocytes in vitro (IC50s = 0.1, 1, and 10 µM for human, guinea pig, and rat hepatocytes,...
(+)-Etomoxir (sodium salt) (+)-Etomoxir (sodium salt)

(+)-Etomoxir (sodium salt)

Reference: 11969-10
€0.00 (tax incl.)
An inhibitor of CPT1; inhibits fatty acid transport into the mitochondria for β-oxidation; inhibits fatty acid oxidation in hepatocytes in vitro (IC50s = 0.1, 1, and 10 µM for human, guinea pig, and rat hepatocytes,...
(+)-Evodiamine (+)-Evodiamine

(+)-Evodiamine

Reference: 16885-50
€0.00 (tax incl.)
A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions; an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC50 = 45 nM), and inhibitor of signaling...
(+)-Evodiamine (+)-Evodiamine

(+)-Evodiamine

Reference: 16885-250
€0.00 (tax incl.)
A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions; an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC50 = 45 nM), and inhibitor of signaling...
(+)-Evodiamine (+)-Evodiamine

(+)-Evodiamine

Reference: 16885-100
€0.00 (tax incl.)
A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions; an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC50 = 45 nM), and inhibitor of signaling...
(+)-Evodiamine (+)-Evodiamine

(+)-Evodiamine

Reference: 16885-1
€0.00 (tax incl.)
A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions; an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC50 = 45 nM), and inhibitor of signaling...
(+)-Fenchol (+)-Fenchol

(+)-Fenchol

Reference: 23162-50
€0.00 (tax incl.)
A monoterpenoid; has been used in the synthesis of other terpenoids and as a chiral building block in organic synthesis of various compounds
(+)-Fenchol (+)-Fenchol

(+)-Fenchol

Reference: 23162-5
€0.00 (tax incl.)
A monoterpenoid; has been used in the synthesis of other terpenoids and as a chiral building block in organic synthesis of various compounds
(+)-Fenchol (+)-Fenchol

(+)-Fenchol

Reference: 23162-10
€0.00 (tax incl.)
A monoterpenoid; has been used in the synthesis of other terpenoids and as a chiral building block in organic synthesis of various compounds
(+)-Gallocatechin (+)-Gallocatechin

(+)-Gallocatechin

Reference: 25125-50
€0.00 (tax incl.)
A polyphenol and flavonoid that has diverse biological activities; inhibits adherence of P. gingivalis onto human buccal epithelial cells by >50% at 250 μg/ml; has antimutagenic properties in UV-irradiated E. coli...
(+)-Gallocatechin (+)-Gallocatechin

(+)-Gallocatechin

Reference: 25125-25
€0.00 (tax incl.)
A polyphenol and flavonoid that has diverse biological activities; inhibits adherence of P. gingivalis onto human buccal epithelial cells by >50% at 250 μg/ml; has antimutagenic properties in UV-irradiated E. coli...
(+)-Gallocatechin (+)-Gallocatechin

(+)-Gallocatechin

Reference: 25125-100
€0.00 (tax incl.)
A polyphenol and flavonoid that has diverse biological activities; inhibits adherence of P. gingivalis onto human buccal epithelial cells by >50% at 250 μg/ml; has antimutagenic properties in UV-irradiated E. coli...
(+)-Geodin (+)-Geodin

(+)-Geodin

Reference: 26421-5
€0.00 (tax incl.)
A fungal metabolite; increases the fibrinolytic activity of BAECs from 50-150 µM; increases 2-deoxyglucose uptake by rat adipocytes from 1-100 µg/ml
(+)-Geodin (+)-Geodin

(+)-Geodin

Reference: 26421-1
€0.00 (tax incl.)
A fungal metabolite; increases the fibrinolytic activity of BAECs from 50-150 µM; increases 2-deoxyglucose uptake by rat adipocytes from 1-100 µg/ml
(+)-Goniothalesdiol (+)-Goniothalesdiol

(+)-Goniothalesdiol

Reference: 10008886-5
€0.00 (tax incl.)
Goniothalesdiol, isolated from the bark of the Malaysian tree G. borneensis, is a tetrahydrofuran compound known to have significant cytotoxic effects against P388 mouse leukemia cells and pesticidal activities
(+)-Goniothalesdiol (+)-Goniothalesdiol

(+)-Goniothalesdiol

Reference: 10008886-10
€0.00 (tax incl.)
Goniothalesdiol, isolated from the bark of the Malaysian tree G. borneensis, is a tetrahydrofuran compound known to have significant cytotoxic effects against P388 mouse leukemia cells and pesticidal activities
(+)-Goniothalesdiol (+)-Goniothalesdiol

(+)-Goniothalesdiol

Reference: 10008886-1
€0.00 (tax incl.)
Goniothalesdiol, isolated from the bark of the Malaysian tree G. borneensis, is a tetrahydrofuran compound known to have significant cytotoxic effects against P388 mouse leukemia cells and pesticidal activities
(+)-Isopulegol (+)-Isopulegol

(+)-Isopulegol

Reference: 23160-500
€0.00 (tax incl.)
A terpenoid that has been found in Cannabis,
(+)-Isopulegol (+)-Isopulegol

(+)-Isopulegol

Reference: 23160-250
€0.00 (tax incl.)
A terpenoid that has been found in Cannabis,
(+)-JQ1 (+)-JQ1

(+)-JQ1

Reference: 11187-5
€0.00 (tax incl.)
Displaces BET proteins from chromatin by competitively binding to the acetyl-lysine recognition pocket of BET bromodomains; binds BRD4 bromodomains 1 and 2 with Kd values of ~50 and 90 nM, respectively

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