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(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: BVT-0307-M025
€0.00 (tax incl.)
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....
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: BVT-0307-M005
€0.00 (tax incl.)
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....
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: BVT-0307-M001
€0.00 (tax incl.)
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....
(+)-Bicuculline (+)-Bicuculline

(+)-Bicuculline

Reference: CDX-B0239-G005
€0.00 (tax incl.)
GABAA receptor antagonist.
(+)-Bicuculline (+)-Bicuculline

(+)-Bicuculline

Reference: CDX-B0239-M500
€0.00 (tax incl.)
GABAA receptor antagonist.
(+)-Bicuculline (+)-Bicuculline

(+)-Bicuculline

Reference: CDX-B0239-M025
€0.00 (tax incl.)
GABAA receptor antagonist.
(+)-Biotin N-hydroxysuccinimide ester (+)-Biotin N-hydroxysuccinimide ester

(+)-Biotin N-hydroxysuccinimide ester

Reference: CDX-B0145-M250
€0.00 (tax incl.)
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...
(+)-Biotin N-hydroxysuccinimide ester (+)-Biotin N-hydroxysuccinimide ester

(+)-Biotin N-hydroxysuccinimide ester

Reference: CDX-B0145-M100
€0.00 (tax incl.)
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...
(+)-Brefeldin A (+)-Brefeldin A

(+)-Brefeldin A

Reference: BVT-0190-M001
€0.00 (tax incl.)
Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor Reviews.
(+)-Brefeldin A (+)-Brefeldin A

(+)-Brefeldin A

Reference: AG-CN2-0018-M025
€0.00 (tax incl.)
Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
(+)-Brefeldin A (+)-Brefeldin A

(+)-Brefeldin A

Reference: AG-CN2-0018-M010
€0.00 (tax incl.)
Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
(+)-Brefeldin A (+)-Brefeldin A

(+)-Brefeldin A

Reference: AG-CN2-0018-M005
€0.00 (tax incl.)
Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor. Reviews.
(+)-Carvone (+)-Carvone

(+)-Carvone

Reference: CDX-C0169-G500
€0.00 (tax incl.)
Terpene standard for GC.
(+)-Carvone (+)-Carvone

(+)-Carvone

Reference: CDX-C0169-G100
€0.00 (tax incl.)
Terpene standard for GC.
(+)-Carvone (+)-Carvone

(+)-Carvone

Reference: CDX-C0169-G005
€0.00 (tax incl.)
Terpene standard for GC.
(+)-Catechin . hydrate (+)-Catechin . hydrate

(+)-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....
(+)-Catechin . hydrate (+)-Catechin . hydrate

(+)-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....
(+)-Etomoxir . Na (+)-Etomoxir . Na

(+)-Etomoxir . Na

Reference: AG-CR1-3688-M025
€0.00 (tax incl.)
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...
(+)-Etomoxir . Na (+)-Etomoxir . Na

(+)-Etomoxir . Na

Reference: AG-CR1-3688-M005
€0.00 (tax incl.)
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...
(+)-Flavipucine (+)-Flavipucine

(+)-Flavipucine

Reference: BVT-0279-M001
€0.00 (tax incl.)
Phytotoxin (Fruit rot toxin). Antibiotic. Antibacterial and antifungal compound.
(+)-JQ1 (+)-JQ1

(+)-JQ1

Reference: SYN-3004-M100
€0.00 (tax incl.)
(+)-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....
(+)-JQ1 (+)-JQ1

(+)-JQ1

Reference: SYN-3004-M050
€0.00 (tax incl.)
(+)-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....
(+)-JQ1 (+)-JQ1

(+)-JQ1

Reference: SYN-3004-M010
€0.00 (tax incl.)
(+)-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....
(+)-JQ1 (+)-JQ1

(+)-JQ1

Reference: SYN-3004-M005
€0.00 (tax incl.)
(+)-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....
(+)-JQ1 (+)-JQ1

(+)-JQ1

Reference: SYN-3004-M001
€0.00 (tax incl.)
(+)-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....
(+)-Rubiginone B2 (+)-Rubiginone B2

(+)-Rubiginone B2

Reference: BVT-0026-M001
€0.00 (tax incl.)
Angucyclinone antibiotic. Antibacterial and antitumor agent. Potentiates the cytotoxicity of vincristine. Antimalarial agent.
(+/-)-C75 (+/-)-C75

(+/-)-C75

Reference: AG-CR1-2904-M005
€0.00 (tax incl.)
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...
(+/-)-C75 (+/-)-C75

(+/-)-C75

Reference: AG-CR1-2904-M001
€0.00 (tax incl.)
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...
(+/-)-Dihydrokaempferol (+/-)-Dihydrokaempferol

(+/-)-Dihydrokaempferol

Reference: CDX-D0442-M050
€0.00 (tax incl.)
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.
(+/-)-Dihydrokaempferol (+/-)-Dihydrokaempferol

(+/-)-Dihydrokaempferol

Reference: CDX-D0442-M010
€0.00 (tax incl.)
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.
(+/-)-Lisofylline (+/-)-Lisofylline

(+/-)-Lisofylline

Reference: CDX-H0117-M050
€0.00 (tax incl.)
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...
(+/-)-Lisofylline (+/-)-Lisofylline

(+/-)-Lisofylline

Reference: CDX-H0117-M010
€0.00 (tax incl.)
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...
(+/-)-Verapamil . hydrochloride (USP Grade) (+/-)-Verapamil . hydrochloride (USP Grade)

(+/-)-Verapamil . hydrochloride (USP Grade)

Reference: AG-CR1-3627-G005
€0.00 (tax incl.)
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...
(+/-)-Verapamil . hydrochloride (USP Grade) (+/-)-Verapamil . hydrochloride (USP Grade)

(+/-)-Verapamil . hydrochloride (USP Grade)

Reference: AG-CR1-3627-G001
€0.00 (tax incl.)
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...
(+/-)-Verapamil . hydrochloride (USP Grade) (+/-)-Verapamil . hydrochloride (USP Grade)

(+/-)-Verapamil . hydrochloride (USP Grade)

Reference: AG-CR1-3627-M100
€0.00 (tax incl.)
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...
(-)-Ageloxime D (-)-Ageloxime D

(-)-Ageloxime D

Reference: AG-CN2-0016-M001
€0.00 (tax incl.)
Quaternary ammonium compound. Antifouling compound. Inhibits biofilm formation but not bacterial growth of Staphylococcus epidermidis. Anticancer compound. Cytotoxic against L5178Y mouse lymphoma cells.
(-)-Arctigenin (-)-Arctigenin

(-)-Arctigenin

Reference: AG-CN2-0530-M050
€0.00 (tax incl.)
Aglycone metabolite of (-)-Arctiin (AG-CN2-0532), isolated from Arctium lappa. Multifunctional natural compound with antioxidant, antibacterial, anti-inflammatory, antidiabetic, neuroprotective, antiproliferative and...
(-)-Arctigenin (-)-Arctigenin

(-)-Arctigenin

Reference: AG-CN2-0530-M010
€0.00 (tax incl.)
Aglycone metabolite of (-)-Arctiin (AG-CN2-0532), isolated from Arctium lappa. Multifunctional natural compound with antioxidant, antibacterial, anti-inflammatory, antidiabetic, neuroprotective, antiproliferative and...
(-)-Arctiin (-)-Arctiin

(-)-Arctiin

Reference: AG-CN2-0532-M050
€0.00 (tax incl.)
Metabolizes into (-)-Arctigenin (AG-CN2-0530). Multifunctional natural compound with photoprotective, anti-inflammatory, antidiabetic, antiproliferative and antiviral activities. Decreasing the production of nitric...
(-)-Arctiin (-)-Arctiin

(-)-Arctiin

Reference: AG-CN2-0532-M010
€0.00 (tax incl.)
Metabolizes into (-)-Arctigenin (AG-CN2-0530). Multifunctional natural compound with photoprotective, anti-inflammatory, antidiabetic, antiproliferative and antiviral activities. Decreasing the production of nitric...
(-)-Bicuculline methiodide (-)-Bicuculline methiodide

(-)-Bicuculline methiodide

Reference: CDX-B0240-M100
€0.00 (tax incl.)
(-)-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...
(-)-Bicuculline methiodide (-)-Bicuculline methiodide

(-)-Bicuculline methiodide

Reference: CDX-B0240-M025
€0.00 (tax incl.)
(-)-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...
(-)-Camphoric acid (-)-Camphoric acid

(-)-Camphoric acid

Reference: CDX-C0144-G010
€0.00 (tax incl.)
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...
(-)-Camphoric acid (-)-Camphoric acid

(-)-Camphoric acid

Reference: CDX-C0144-G001
€0.00 (tax incl.)
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...
(-)-Catechin (-)-Catechin

(-)-Catechin

Reference: CDX-C0453-M025
€0.00 (tax incl.)
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...
(-)-Catechin (-)-Catechin

(-)-Catechin

Reference: CDX-C0453-M005
€0.00 (tax incl.)
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...
(-)-Cytisine (-)-Cytisine

(-)-Cytisine

Reference: CDX-C0228-G005
€0.00 (tax incl.)
Pyridine-like alkaloid. Nicotine agonist. Potent agonist at alpha3beta4 and alpha7 nicotinic acetylcholine receptors and partial agonist at alpha4beta2 nicotinic acetylcholine receptors. Shows analgesic,...
(-)-Cytisine (-)-Cytisine

(-)-Cytisine

Reference: CDX-C0228-M500
€0.00 (tax incl.)
Pyridine-like alkaloid. Nicotine agonist. Potent agonist at alpha3beta4 and alpha7 nicotinic acetylcholine receptors and partial agonist at alpha4beta2 nicotinic acetylcholine receptors. Shows analgesic,...
(-)-Cytisine (-)-Cytisine

(-)-Cytisine

Reference: CDX-C0228-M100
€0.00 (tax incl.)
Pyridine-like alkaloid. Nicotine agonist. Potent agonist at alpha3beta4 and alpha7 nicotinic acetylcholine receptors and partial agonist at alpha4beta2 nicotinic acetylcholine receptors. Shows analgesic,...
(-)-Epicatechin (-)-Epicatechin

(-)-Epicatechin

Reference: CDX-E0231-M025
€0.00 (tax incl.)
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...
(-)-Epicatechin (-)-Epicatechin

(-)-Epicatechin

Reference: CDX-E0231-M005
€0.00 (tax incl.)
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...
(-)-Epicatechin gallate (-)-Epicatechin gallate

(-)-Epicatechin gallate

Reference: CDX-E0181-M010
€0.00 (tax incl.)
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...
(-)-Epigallocatechin (-)-Epigallocatechin

(-)-Epigallocatechin

Reference: CDX-E0182-M010
€0.00 (tax incl.)
(-)-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...
(-)-Epigallocatechin gallate (-)-Epigallocatechin gallate

(-)-Epigallocatechin gallate

Reference: CDX-E0128-M010
€0.00 (tax incl.)
(-)-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...
(-)-Epigallocatechin gallate (-)-Epigallocatechin gallate

(-)-Epigallocatechin gallate

Reference: AG-CN2-0063-M100
€0.00 (tax incl.)
Potent anticancer compound. Anti-angiogenic. VEGF, VE-cadherin phosphorylation, matrix metalloproteinase and urokinase-plasminogen activator (uPA) inhibitor. Anti-inflammatory. NF-kappaB inhibitor. Modulates chronic...
(-)-Epigallocatechin gallate (-)-Epigallocatechin gallate

(-)-Epigallocatechin gallate

Reference: AG-CN2-0063-M025
€0.00 (tax incl.)
Potent anticancer compound. Anti-angiogenic. VEGF, VE-cadherin phosphorylation, matrix metalloproteinase and urokinase-plasminogen activator (uPA) inhibitor. Anti-inflammatory. NF-kappaB inhibitor. Modulates chronic...
(-)-Gallocatechin gallate (-)-Gallocatechin gallate

(-)-Gallocatechin gallate

Reference: CDX-G0197-M005
€0.00 (tax incl.)
(-)-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...
(-)-Huperzine A (-)-Huperzine A

(-)-Huperzine A

Reference: CDX-H0208-M025
€0.00 (tax incl.)
Huperzine A is a natural sesquiterpene alkaloid. It showns neuroprotective activity. It is a potent acetylcholinesterase (AChE) inhibitor and displays oral AChE inhibitory activity in animals. Huperzine A has...
(-)-Indolactam V (-)-Indolactam V

(-)-Indolactam V

Reference: AG-CR1-0041-M001
€0.00 (tax incl.)
Tumor promoter. Protein kinase C (PKC) inducer. Mitogenesis activator. Differentiation inducer.
(-)-Indolactam V (-)-Indolactam V

(-)-Indolactam V

Reference: AG-CR1-0041-C300
€0.00 (tax incl.)
Tumor promoter. Protein kinase C (PKC) inducer. Mitogenesis activator. Differentiation inducer.
(-)-Mitorubrinic acid (-)-Mitorubrinic acid

(-)-Mitorubrinic acid

Reference: AG-CN2-0505-M001
€0.00 (tax incl.)
Azaphilone fungal metabolite. Induces formation of chlamydospore-like cells in fungi. Trypsin inhibitor (IC50=16µg/ml). Mitorubrinic acid was shown to be a virulence factor of Penicillium marneffei by improving its...
(-)-Viriditoxin (-)-Viriditoxin

(-)-Viriditoxin

Reference: AG-CN2-0471-C500
€0.00 (tax incl.)
Antibiotic. Exhibits broad activity against Gram-positive bacteria. Bacterial cell division protein FtsZ inhibitor (IC50=8.2µg/ml). Inhibits the GTPase activity of FtsZ in vitro (IC50=7.0µg/ml). Induces apoptosis and...
(25S)-delta7-Dafachronic acid [UPF-1404] (25S)-delta7-Dafachronic acid [UPF-1404]

(25S)-delta7-Dafachronic acid [UPF-1404]

Reference: AG-CN2-0014-C100
€0.00 (tax incl.)
Ligand of DAF-12, an orphan nuclear receptor, that regulates dauer diapause, reproductive development, fat metabolism, and life span (life cycle) in parasitic nematodes. Sterol-derived hormone. Blocks formation of...
(3S,6R)-Lateritin (3S,6R)-Lateritin

(3S,6R)-Lateritin

Reference: AG-CN2-0042-M001
€0.00 (tax incl.)
N-methylated peptide that is structurally equivalent to a monomer of beauvericin (Prod. No. AG-CN2-0043). Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. Platelet aggregation inhibitor. Antimicrobial. Note: The...
(5(6)-ROX (5(6)-ROX

(5(6)-ROX

Reference: CDX-C0012-G001
€0.00 (tax incl.)
May be used as a fluorescent dye in nucleic acid analytical research applications.
(5(6)-ROX (5(6)-ROX

(5(6)-ROX

Reference: CDX-C0012-M100
€0.00 (tax incl.)
May be used as a fluorescent dye in nucleic acid analytical research applications.
(5(6)-ROX (5(6)-ROX

(5(6)-ROX

Reference: CDX-C0012-M025
€0.00 (tax incl.)
May be used as a fluorescent dye in nucleic acid analytical research applications.
(Boc-Cys-OH)2 (Boc-Cys-OH)2

(Boc-Cys-OH)2

Reference: CDX-B0224-G025
€0.00 (tax incl.)
Amino acid protected by tert-butoxycarbonyl (Boc) group. Used as a reactant in peptide synthesis. Used to obtain asymmetric cystine peptides by enzymatic catalysis with immobilized papain. Used as educt for obtaining...
(Boc-Cys-OH)2 (Boc-Cys-OH)2

(Boc-Cys-OH)2

Reference: CDX-B0224-G005
€0.00 (tax incl.)
Amino acid protected by tert-butoxycarbonyl (Boc) group. Used as a reactant in peptide synthesis. Used to obtain asymmetric cystine peptides by enzymatic catalysis with immobilized papain. Used as educt for obtaining...
(E)-8-Methyl-6-nonenoic acid (E)-8-Methyl-6-nonenoic acid

(E)-8-Methyl-6-nonenoic acid

Reference: CDX-M0209-G001
€0.00 (tax incl.)
Intermediate of the capsaicin biosynthesis. Fatty acid derivative from leucine/valine pathway. Plays a crucial role in determining the efficacy of capsaicin levels. The quantity of (E)-8-Methyl-6-nonenoic acid...
(E)-8-Methyl-6-nonenoic acid (E)-8-Methyl-6-nonenoic acid

(E)-8-Methyl-6-nonenoic acid

Reference: CDX-M0209-M500
€0.00 (tax incl.)
Intermediate of the capsaicin biosynthesis. Fatty acid derivative from leucine/valine pathway. Plays a crucial role in determining the efficacy of capsaicin levels. The quantity of (E)-8-Methyl-6-nonenoic acid...
(R)-(+)-2-Phenyl-1-propanol (R)-(+)-2-Phenyl-1-propanol

(R)-(+)-2-Phenyl-1-propanol

Reference: CDX-P0385-G001
€0.00 (tax incl.)
Important building block and synthetic intermediate reagent for synthesis of chiral compounds.
(R)-3-Hydroxybutyric acid (R)-3-Hydroxybutyric acid

(R)-3-Hydroxybutyric acid

Reference: AG-CR1-3616-M100
€0.00 (tax incl.)
Key metabolite of the ketolytic pathway generating acetyl-CoA. Stereoselective product of D-3-hydroxybutyrate dehydreogenase. Clinically and physiologically significant stereoisomer. Energy carrier from adipocytes to...
(R)-3-Hydroxybutyric acid (R)-3-Hydroxybutyric acid

(R)-3-Hydroxybutyric acid

Reference: AG-CR1-3616-M025
€0.00 (tax incl.)
Key metabolite of the ketolytic pathway generating acetyl-CoA. Stereoselective product of D-3-hydroxybutyrate dehydreogenase. Clinically and physiologically significant stereoisomer. Energy carrier from adipocytes to...
(R)-3-Hydroxymyristic acid (R)-3-Hydroxymyristic acid

(R)-3-Hydroxymyristic acid

Reference: CDX-H0114-G001
€0.00 (tax incl.)
Hydroxy fatty acid used to study its role in biological processes such as oxidative stress, inflammation and insulin resistance. Used in endotoxin and lipid A research, since it is one of two major components of...
(R)-3-Hydroxymyristic acid (R)-3-Hydroxymyristic acid

(R)-3-Hydroxymyristic acid

Reference: CDX-H0114-M250
€0.00 (tax incl.)
Hydroxy fatty acid used to study its role in biological processes such as oxidative stress, inflammation and insulin resistance. Used in endotoxin and lipid A research, since it is one of two major components of...
(R)-BI-2536 (R)-BI-2536

(R)-BI-2536

Reference: SYN-1019-M100
€0.00 (tax incl.)
Polo-like kinase 1 (Plk1) is a regulator of the cell cycle that has been implicated in the pathology of many cancers. BI-2536 is a potent and selective small-molecule inhibitor of mammalian Plk1. It has inhibitory...
(R)-BI-2536 (R)-BI-2536

(R)-BI-2536

Reference: SYN-1019-M050
€0.00 (tax incl.)
Polo-like kinase 1 (Plk1) is a regulator of the cell cycle that has been implicated in the pathology of many cancers. BI-2536 is a potent and selective small-molecule inhibitor of mammalian Plk1. It has inhibitory...
(R)-BI-2536 (R)-BI-2536

(R)-BI-2536

Reference: SYN-1019-M010
€0.00 (tax incl.)
Polo-like kinase 1 (Plk1) is a regulator of the cell cycle that has been implicated in the pathology of many cancers. BI-2536 is a potent and selective small-molecule inhibitor of mammalian Plk1. It has inhibitory...
(R)-BI-2536 (R)-BI-2536

(R)-BI-2536

Reference: SYN-1019-M005
€0.00 (tax incl.)
Polo-like kinase 1 (Plk1) is a regulator of the cell cycle that has been implicated in the pathology of many cancers. BI-2536 is a potent and selective small-molecule inhibitor of mammalian Plk1. It has inhibitory...
(R)-BI-2536 (R)-BI-2536

(R)-BI-2536

Reference: SYN-1019-M001
€0.00 (tax incl.)
Polo-like kinase 1 (Plk1) is a regulator of the cell cycle that has been implicated in the pathology of many cancers. BI-2536 is a potent and selective small-molecule inhibitor of mammalian Plk1. It has inhibitory...
(R)-CR8 (R)-CR8

(R)-CR8

Reference: AG-MR-C0003-M050
€0.00 (tax incl.)
Potent and selective inhibitor of cyclin dependent kinases CDK1, CDK2, CDK5, CDK7 and CDK9. Apoptosis inducer. Inhibits the proliferation of various cancer cell lines. Casein kinase 1 (CK1delta/epsilon) and glycogen...

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