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(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: B7832-25
€0.00 (tax incl.)
tetracyclic diterpene antibiotic
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: B7832-5
€0.00 (tax incl.)
tetracyclic diterpene antibiotic
(+)-Aphidicolin (+)-Aphidicolin

(+)-Aphidicolin

Reference: B7832-1
€0.00 (tax incl.)
tetracyclic diterpene antibiotic
(+)-Apogossypol (+)-Apogossypol

(+)-Apogossypol

Reference: B4902-5.1
€0.00 (tax incl.)
inhibitor of Bcl-2 family proteins
(+)-Apogossypol (+)-Apogossypol

(+)-Apogossypol

Reference: B4902-10
€0.00 (tax incl.)
inhibitor of Bcl-2 family proteins
(+)-Apogossypol (+)-Apogossypol

(+)-Apogossypol

Reference: B4902-5
€0.00 (tax incl.)
inhibitor of Bcl-2 family proteins
(+)-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.
(+)-Bicuculline (+)-Bicuculline

(+)-Bicuculline

Reference: N1592-250
€0.00 (tax incl.)
GABAA receptor antagonist,competitve and classical
(+)-Bicuculline (+)-Bicuculline

(+)-Bicuculline

Reference: N1592-100
€0.00 (tax incl.)
GABAA receptor antagonist,competitve and classical
(+)-Bicuculline (+)-Bicuculline

(+)-Bicuculline

Reference: N1592-5.1
€0.00 (tax incl.)
GABAA receptor antagonist,competitve and classical
(+)-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...
(+)-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....
(+)-Catechin hydrate (+)-Catechin hydrate

(+)-Catechin hydrate

Reference: N1692-5.1
€0.00 (tax incl.)
Antioxidant flavonoid with various bioactivities
(+)-Catechin hydrate (+)-Catechin hydrate

(+)-Catechin hydrate

Reference: N1692-20
€0.00 (tax incl.)
Antioxidant flavonoid with various bioactivities
(+)-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...
(+)-Fluprostenol (+)-Fluprostenol

(+)-Fluprostenol

Reference: B7680-1
€0.00 (tax incl.)
Prostaglandin F2α (FP) receptor agonist
(+)-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....
(+)-Ketoconazole (+)-Ketoconazole

(+)-Ketoconazole

Reference: B1240-1000
€0.00 (tax incl.)
Potent inhibitor of cytochrome P450c17
(+)-Ketoconazole (+)-Ketoconazole

(+)-Ketoconazole

Reference: B1240-500
€0.00 (tax incl.)
Potent inhibitor of cytochrome P450c17
(+)-Ketoconazole (+)-Ketoconazole

(+)-Ketoconazole

Reference: B1240-5.1
€0.00 (tax incl.)
Potent inhibitor of cytochrome P450c17
(+)-MK 801 (+)-MK 801

(+)-MK 801

Reference: A3100-50
€0.00 (tax incl.)
Potent NMDA antagonist
(+)-MK 801 (+)-MK 801

(+)-MK 801

Reference: A3100-5.1
€0.00 (tax incl.)
Potent NMDA antagonist
(+)-MK 801 (+)-MK 801

(+)-MK 801

Reference: A3100-10
€0.00 (tax incl.)
Potent NMDA antagonist
(+)-trans-C75 (+)-trans-C75

(+)-trans-C75

Reference: C4741-10
€0.00 (tax incl.)
enantiomer of C75, a fatty acid synthase (FAS) inhibitor
(+)-trans-C75 (+)-trans-C75

(+)-trans-C75

Reference: C4741-5
€0.00 (tax incl.)
enantiomer of C75, a fatty acid synthase (FAS) inhibitor
(+)-trans-C75 (+)-trans-C75

(+)-trans-C75

Reference: C4741-1
€0.00 (tax incl.)
enantiomer of C75, a fatty acid synthase (FAS) inhibitor
(+)-Usniacin (+)-Usniacin

(+)-Usniacin

Reference: B3661-5.1
€0.00 (tax incl.)
Naturally occurring dibenzofuran derivative
(+)-Usniacin (+)-Usniacin

(+)-Usniacin

Reference: B3661-50
€0.00 (tax incl.)
Naturally occurring dibenzofuran derivative
(+/-)-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...

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