Reagents (513)

A 83-01

Reference: 9001799-10

€0.00 (tax incl.)

An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respectively); blocks the phosphorylation of SMAD2/3 and inhibits TGF-β-induced epithelial-to-mesenchymal transition; used to reprogram fibroblasts...

A 83-01

Reference: 9001799-25

€0.00 (tax incl.)

An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respectively); blocks the phosphorylation of SMAD2/3 and inhibits TGF-β-induced epithelial-to-mesenchymal transition; used to reprogram fibroblasts...

A 83-01

Reference: 9001799-5

€0.00 (tax incl.)

An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respectively); blocks the phosphorylation of SMAD2/3 and inhibits TGF-β-induced epithelial-to-mesenchymal transition; used to reprogram fibroblasts...

N-Desethyl Vardenafil

Reference: 9001800-1

€0.00 (tax incl.)

A metabolite of vardenafil that is formed by the action of CYP3A4 and CYP3A5

N-Desethyl Vardenafil

Reference: 9001800-5

€0.00 (tax incl.)

A metabolite of vardenafil that is formed by the action of CYP3A4 and CYP3A5

N-Desethyl Vardenafil

Reference: 9001800-500

€0.00 (tax incl.)

A metabolite of vardenafil that is formed by the action of CYP3A4 and CYP3A5

Levetiracetam

Reference: 9001820-10

€0.00 (tax incl.)

An antiepileptic agent; binds to the synaptic vesicle protein SV2A (IC50 = 1.99 μM); suppresses seizures in fully kindled rats

Levetiracetam

Reference: 9001820-100

€0.00 (tax incl.)

An antiepileptic agent; binds to the synaptic vesicle protein SV2A (IC50 = 1.99 μM); suppresses seizures in fully kindled rats

Levetiracetam

Reference: 9001820-5

€0.00 (tax incl.)

An antiepileptic agent; binds to the synaptic vesicle protein SV2A (IC50 = 1.99 μM); suppresses seizures in fully kindled rats

Levetiracetam

Reference: 9001820-50

€0.00 (tax incl.)

An antiepileptic agent; binds to the synaptic vesicle protein SV2A (IC50 = 1.99 μM); suppresses seizures in fully kindled rats

Dibutyl-3-Hydroxybutyl Phosphate

Reference: 9001825-1

€0.00 (tax incl.)

A compound produced from the metabolism of the organophosphorus solvent, TBP

Dibutyl-3-Hydroxybutyl Phosphate

Reference: 9001825-10

€0.00 (tax incl.)

A compound produced from the metabolism of the organophosphorus solvent, TBP

Dibutyl-3-Hydroxybutyl Phosphate

Reference: 9001825-25

€0.00 (tax incl.)

A compound produced from the metabolism of the organophosphorus solvent, TBP

Dibutyl-3-Hydroxybutyl Phosphate

Reference: 9001825-5

€0.00 (tax incl.)

A compound produced from the metabolism of the organophosphorus solvent, TBP

Stem Cell Small Molecule Screening Library (96-Well)

Reference: 9001827-50

€0.00 (tax incl.)

This small molecule library contains molecules that are known either to induce differentiation, to maintain self-renewal and proliferation, or to improve the reprogramming efficiency of various stem cell populations.

RSC-133

Reference: 9001839-1

€0.00 (tax incl.)

Promotes the reprogramming of human somatic cells to pluripotent stem cells; increases the number of human foreskin fibroblasts that express alkaline phosphatase when used at 10 μM with four standard reprogramming...

RSC-133

Reference: 9001839-10

€0.00 (tax incl.)

Promotes the reprogramming of human somatic cells to pluripotent stem cells; increases the number of human foreskin fibroblasts that express alkaline phosphatase when used at 10 μM with four standard reprogramming...

RSC-133

Reference: 9001839-25

€0.00 (tax incl.)

Promotes the reprogramming of human somatic cells to pluripotent stem cells; increases the number of human foreskin fibroblasts that express alkaline phosphatase when used at 10 μM with four standard reprogramming...

RSC-133

Reference: 9001839-5

€0.00 (tax incl.)

Promotes the reprogramming of human somatic cells to pluripotent stem cells; increases the number of human foreskin fibroblasts that express alkaline phosphatase when used at 10 μM with four standard reprogramming...

cis-6-Hexadecenoic Acid

Reference: 9001845-10

€0.00 (tax incl.)

A monounsaturated fatty acid; one of the primary fatty acids in human skin; levels are increased in isolated sebum from the face and back of patients with acne; levels are decreased in the non-lesional skin and...

cis-6-Hexadecenoic Acid

Reference: 9001845-25

€0.00 (tax incl.)

A monounsaturated fatty acid; one of the primary fatty acids in human skin; levels are increased in isolated sebum from the face and back of patients with acne; levels are decreased in the non-lesional skin and...

cis-6-Hexadecenoic Acid

Reference: 9001845-5

€0.00 (tax incl.)

A monounsaturated fatty acid; one of the primary fatty acids in human skin; levels are increased in isolated sebum from the face and back of patients with acne; levels are decreased in the non-lesional skin and...

Propionyl-L-carnitine (chloride)

Reference: 9001873-100

€0.00 (tax incl.)

A carnitine derivative; increases the basal release of PGE2 and 6-keto prostaglandin F1α in carrageenan-stimulated isolated rat peritoneal cells contaminated with neutrophils; increases the basal release of...

Propionyl-L-carnitine (chloride)

Reference: 9001873-25

€0.00 (tax incl.)

A carnitine derivative; increases the basal release of PGE2 and 6-keto prostaglandin F1α in carrageenan-stimulated isolated rat peritoneal cells contaminated with neutrophils; increases the basal release of...

Propionyl-L-carnitine (chloride)

Reference: 9001873-50

€0.00 (tax incl.)

A carnitine derivative; increases the basal release of PGE2 and 6-keto prostaglandin F1α in carrageenan-stimulated isolated rat peritoneal cells contaminated with neutrophils; increases the basal release of...

PF-299804

Reference: 9001879-1

€0.00 (tax incl.)

An irreversible pan-ErbB receptor tyrosine kinase inhibitor (IC50s = 6, 45.7, and 73.7 nM for ErbB1, ErbB2, and ErbB4, respectively); demonstrates antitumor activity in various tumor xenograft models expressing either...

PF-299804

Reference: 9001879-10

€0.00 (tax incl.)

An irreversible pan-ErbB receptor tyrosine kinase inhibitor (IC50s = 6, 45.7, and 73.7 nM for ErbB1, ErbB2, and ErbB4, respectively); demonstrates antitumor activity in various tumor xenograft models expressing either...

PF-299804

Reference: 9001879-5

€0.00 (tax incl.)

An irreversible pan-ErbB receptor tyrosine kinase inhibitor (IC50s = 6, 45.7, and 73.7 nM for ErbB1, ErbB2, and ErbB4, respectively); demonstrates antitumor activity in various tumor xenograft models expressing either...

PF-299804

Reference: 9001879-50

€0.00 (tax incl.)

An irreversible pan-ErbB receptor tyrosine kinase inhibitor (IC50s = 6, 45.7, and 73.7 nM for ErbB1, ErbB2, and ErbB4, respectively); demonstrates antitumor activity in various tumor xenograft models expressing either...

(±)-O-Desmethyl Venlafaxine

Reference: 9001881-10

€0.00 (tax incl.)

A CYP2D6 metabolite of venlafaxine that inhibits the human serotonin and norepinephrine transporters (IC50s = 47.3 and 531.3 nM, respectively)

(±)-O-Desmethyl Venlafaxine

Reference: 9001881-25

€0.00 (tax incl.)

A CYP2D6 metabolite of venlafaxine that inhibits the human serotonin and norepinephrine transporters (IC50s = 47.3 and 531.3 nM, respectively)

(±)-O-Desmethyl Venlafaxine

Reference: 9001881-5

€0.00 (tax incl.)

A CYP2D6 metabolite of venlafaxine that inhibits the human serotonin and norepinephrine transporters (IC50s = 47.3 and 531.3 nM, respectively)

(±)-O-Desmethyl Venlafaxine

Reference: 9001881-50

€0.00 (tax incl.)

A CYP2D6 metabolite of venlafaxine that inhibits the human serotonin and norepinephrine transporters (IC50s = 47.3 and 531.3 nM, respectively)

Saquinavir (mesylate)

Reference: 9001893-10

€0.00 (tax incl.)

An HIV protease inhibitor (Kis = 0.12 and 1 and HIV-2 protease, respectively) that exhibits antiviral activity with low cytotoxicity

Saquinavir (mesylate)

Reference: 9001893-25

€0.00 (tax incl.)

An HIV protease inhibitor (Kis = 0.12 and 1 and HIV-2 protease, respectively) that exhibits antiviral activity with low cytotoxicity

Saquinavir (mesylate)

Reference: 9001893-5

€0.00 (tax incl.)

An HIV protease inhibitor (Kis = 0.12 and 1 and HIV-2 protease, respectively) that exhibits antiviral activity with low cytotoxicity

Saquinavir (mesylate)

Reference: 9001893-50

€0.00 (tax incl.)

An HIV protease inhibitor (Kis = 0.12 and 1 and HIV-2 protease, respectively) that exhibits antiviral activity with low cytotoxicity

5-Aminolevulinic Acid (hydrochloride)

Reference: 9001902-1

€0.00 (tax incl.)

A precursor in the biosynthesis of porphyrins; used in photodynamic therapy for a range of dermatological conditions, cancers, and other diseases; also used in fluorescence-based identification of tumor tissue for...

5-Aminolevulinic Acid (hydrochloride)

Reference: 9001902-5

€0.00 (tax incl.)

A precursor in the biosynthesis of porphyrins; used in photodynamic therapy for a range of dermatological conditions, cancers, and other diseases; also used in fluorescence-based identification of tumor tissue for...

5-Aminolevulinic Acid (hydrochloride)

Reference: 9001902-500

€0.00 (tax incl.)

A precursor in the biosynthesis of porphyrins; used in photodynamic therapy for a range of dermatological conditions, cancers, and other diseases; also used in fluorescence-based identification of tumor tissue for...

ML-336

Reference: 9001920-1

€0.00 (tax incl.)

A quinazolinone-based compound that has been shown to inhibit a VEEV-induced cytopathic effect in three strains of the virus (IC50s = 32, 20, and 41 nM for TC-83, V3526, and Trinidad donkey strains, respectively)

ML-336

Reference: 9001920-10

€0.00 (tax incl.)

A quinazolinone-based compound that has been shown to inhibit a VEEV-induced cytopathic effect in three strains of the virus (IC50s = 32, 20, and 41 nM for TC-83, V3526, and Trinidad donkey strains, respectively)

ML-336

Reference: 9001920-25

€0.00 (tax incl.)

A quinazolinone-based compound that has been shown to inhibit a VEEV-induced cytopathic effect in three strains of the virus (IC50s = 32, 20, and 41 nM for TC-83, V3526, and Trinidad donkey strains, respectively)

ML-336

Reference: 9001920-5

€0.00 (tax incl.)

A quinazolinone-based compound that has been shown to inhibit a VEEV-induced cytopathic effect in three strains of the virus (IC50s = 32, 20, and 41 nM for TC-83, V3526, and Trinidad donkey strains, respectively)

ZK 159222

Reference: 9001925-500

€0.00 (tax incl.)

An antagonist of the vitamin D receptor; inhibits VDR-mediated target gene activation at 300 and 1,000 nM in reporter assays; decreases MacCM-induced secretion of IL-1β, IL-6, IL-8, CCL2, and RANTES in preadipocytes...

(R)-nitro-Blebbistatin

Reference: 9001935-1

€0.00 (tax incl.)

A more stable form of (+)-blebbistatin, the inactive form of blebbistatin; has the same stereochemistry as the inactive (+)-blebbistatin enantiomer

(R)-nitro-Blebbistatin

Reference: 9001935-10

€0.00 (tax incl.)

A more stable form of (+)-blebbistatin, the inactive form of blebbistatin; has the same stereochemistry as the inactive (+)-blebbistatin enantiomer

(R)-nitro-Blebbistatin

Reference: 9001935-5

€0.00 (tax incl.)

A more stable form of (+)-blebbistatin, the inactive form of blebbistatin; has the same stereochemistry as the inactive (+)-blebbistatin enantiomer

12(S)-HETE-19,20-alkyne

Reference: 9001937-100

€0.00 (tax incl.)

A form of 12(S)-HETE with an ω-terminal alkyne for use in click chemistry reactions

12(S)-HETE-19,20-alkyne

Reference: 9001937-25

€0.00 (tax incl.)

A form of 12(S)-HETE with an ω-terminal alkyne for use in click chemistry reactions

12(S)-HETE-19,20-alkyne

Reference: 9001937-50

€0.00 (tax incl.)

A form of 12(S)-HETE with an ω-terminal alkyne for use in click chemistry reactions

MCHB-1

Reference: 9001949-1

€0.00 (tax incl.)

A CB2 receptor agonist; selective for CB2 over CB1 (Kis = 3.7 and 110 nM, respectively),

MCHB-1

Reference: 9001949-10

€0.00 (tax incl.)

A CB2 receptor agonist; selective for CB2 over CB1 (Kis = 3.7 and 110 nM, respectively),

MCHB-1

Reference: 9001949-5

€0.00 (tax incl.)

A CB2 receptor agonist; selective for CB2 over CB1 (Kis = 3.7 and 110 nM, respectively),

AF3485

Reference: 9001962-1

€0.00 (tax incl.)

A selective inhibitor of mPGES-1, blocking the synthesis of PGE2 but not PGF2α in A549 cells stimulated with IL-1β (IC50s = 2.9 and >100 µM, respectively); absorbed through enterocytes, metabolically stable in human...

AF3485

Reference: 9001962-10

€0.00 (tax incl.)

A selective inhibitor of mPGES-1, blocking the synthesis of PGE2 but not PGF2α in A549 cells stimulated with IL-1β (IC50s = 2.9 and >100 µM, respectively); absorbed through enterocytes, metabolically stable in human...

AF3485

Reference: 9001962-5

€0.00 (tax incl.)

A selective inhibitor of mPGES-1, blocking the synthesis of PGE2 but not PGF2α in A549 cells stimulated with IL-1β (IC50s = 2.9 and >100 µM, respectively); absorbed through enterocytes, metabolically stable in human...

BCATc Inhibitor 2

Reference: 9002002-1

€0.00 (tax incl.)

A sulfonyl hydrazide that inhibits BCATc (IC50s = 0.81 and 0.2 µM in human and rat, respectively) with 15-fold selectivity over BCATm; blocks calcium influx into neurons (IC50 = 4.8 µM) following inhibition of...

BCATc Inhibitor 2

Reference: 9002002-10

€0.00 (tax incl.)

A sulfonyl hydrazide that inhibits BCATc (IC50s = 0.81 and 0.2 µM in human and rat, respectively) with 15-fold selectivity over BCATm; blocks calcium influx into neurons (IC50 = 4.8 µM) following inhibition of...

BCATc Inhibitor 2

Reference: 9002002-5

€0.00 (tax incl.)

A sulfonyl hydrazide that inhibits BCATc (IC50s = 0.81 and 0.2 µM in human and rat, respectively) with 15-fold selectivity over BCATm; blocks calcium influx into neurons (IC50 = 4.8 µM) following inhibition of...

BCATc Inhibitor 2

Reference: 9002002-50

€0.00 (tax incl.)

A sulfonyl hydrazide that inhibits BCATc (IC50s = 0.81 and 0.2 µM in human and rat, respectively) with 15-fold selectivity over BCATm; blocks calcium influx into neurons (IC50 = 4.8 µM) following inhibition of...

Mecillinam

Reference: 9002008-1

€0.00 (tax incl.)

A β-lactam antibiotic; active against Gram-negative bacteria, including E. coli, K. pneumoniae, and N. gonorrhoeae (MIC90s = 4, 8, and 1 μg/ml, respectively); active against clinical isolates of E. coli, K....

Mecillinam

Reference: 9002008-10

€0.00 (tax incl.)

A β-lactam antibiotic; active against Gram-negative bacteria, including E. coli, K. pneumoniae, and N. gonorrhoeae (MIC90s = 4, 8, and 1 μg/ml, respectively); active against clinical isolates of E. coli, K....

Mecillinam

Reference: 9002008-500

€0.00 (tax incl.)

A β-lactam antibiotic; active against Gram-negative bacteria, including E. coli, K. pneumoniae, and N. gonorrhoeae (MIC90s = 4, 8, and 1 μg/ml, respectively); active against clinical isolates of E. coli, K....

Cephalexin

Reference: 9002009-1

€0.00 (tax incl.)

A cephalosporin antibiotic that is active against most Gram-positive cocci, including penicillinase-producing Staphylococci, and against Gram-negative bacteria such as N. gonorrhoeae, E. coli, K. pneumonia,...

Cephalexin

Reference: 9002009-10

€0.00 (tax incl.)

A cephalosporin antibiotic that is active against most Gram-positive cocci, including penicillinase-producing Staphylococci, and against Gram-negative bacteria such as N. gonorrhoeae, E. coli, K. pneumonia,...

Cephalexin

Reference: 9002009-25

€0.00 (tax incl.)

A cephalosporin antibiotic that is active against most Gram-positive cocci, including penicillinase-producing Staphylococci, and against Gram-negative bacteria such as N. gonorrhoeae, E. coli, K. pneumonia,...

Cephalexin

Reference: 9002009-5

€0.00 (tax incl.)

A cephalosporin antibiotic that is active against most Gram-positive cocci, including penicillinase-producing Staphylococci, and against Gram-negative bacteria such as N. gonorrhoeae, E. coli, K. pneumonia,...

Seratrodast

Reference: 9002014-10

€0.00 (tax incl.)

A potent antagonist of the TXA2 receptor, blocking specific binding of U-46619 to platelets with an IC50 value of 7.4 nM and platelet aggregation induced by U-44069 with an IC50 value of 350 nM; commonly used to study...

Seratrodast

Reference: 9002014-25

€0.00 (tax incl.)

A potent antagonist of the TXA2 receptor, blocking specific binding of U-46619 to platelets with an IC50 value of 7.4 nM and platelet aggregation induced by U-44069 with an IC50 value of 350 nM; commonly used to study...

Seratrodast

Reference: 9002014-50

€0.00 (tax incl.)

A potent antagonist of the TXA2 receptor, blocking specific binding of U-46619 to platelets with an IC50 value of 7.4 nM and platelet aggregation induced by U-44069 with an IC50 value of 350 nM; commonly used to study...

Abz-Val-Ala-Asp-Nva-Arg-Asp-Arg-Gln-EDDnp (trifluoroacetate salt)

Reference: 9002021-1

€0.00 (tax incl.)

A fluorescence-quenched peptide substrate for human proteinase 3 (ex = 320 nm; em = 420 nm)

Enniatin Complex

Reference: 9002040-10

€0.00 (tax incl.)

A mixture of cyclohexadepsipeptides commonly isolated from fungi that act as ionophores, forming pores in cellular membranes to allow selective ion transport; exhibits antimicrobial activity against a variety of...

Enniatin Complex

Reference: 9002040-50

€0.00 (tax incl.)

A mixture of cyclohexadepsipeptides commonly isolated from fungi that act as ionophores, forming pores in cellular membranes to allow selective ion transport; exhibits antimicrobial activity against a variety of...

BODIPY-aminoacetaldehyde diethyl acetal

Reference: 9002056-1

€0.00 (tax incl.)

A stable precursor to the fluorescent ALDH substrate BAAA; converted under acidic conditions to BAAA, which is cell-permeant and is converted intracellularly to BAA, which can be used to identify cells with high ALDH...

BODIPY-aminoacetaldehyde diethyl acetal

Reference: 9002056-100

€0.00 (tax incl.)

A stable precursor to the fluorescent ALDH substrate BAAA; converted under acidic conditions to BAAA, which is cell-permeant and is converted intracellularly to BAA, which can be used to identify cells with high ALDH...

BODIPY-aminoacetaldehyde diethyl acetal

Reference: 9002056-50

€0.00 (tax incl.)

A stable precursor to the fluorescent ALDH substrate BAAA; converted under acidic conditions to BAAA, which is cell-permeant and is converted intracellularly to BAA, which can be used to identify cells with high ALDH...

BODIPY-aminoacetaldehyde diethyl acetal

Reference: 9002056-500

€0.00 (tax incl.)

A stable precursor to the fluorescent ALDH substrate BAAA; converted under acidic conditions to BAAA, which is cell-permeant and is converted intracellularly to BAA, which can be used to identify cells with high ALDH...

WH-4-023

Reference: 9002067-1

€0.00 (tax incl.)

A selective inhibitor of the Src family of non-receptor tyrosine kinases (IC50s = 2 and 6 nM for Lck and Src, respectively); used in combination with PD 0325901, CHIR99021, and SB-590885 to support self-renewal of...

WH-4-023

Reference: 9002067-10

€0.00 (tax incl.)

A selective inhibitor of the Src family of non-receptor tyrosine kinases (IC50s = 2 and 6 nM for Lck and Src, respectively); used in combination with PD 0325901, CHIR99021, and SB-590885 to support self-renewal of...

WH-4-023

Reference: 9002067-25

€0.00 (tax incl.)

A selective inhibitor of the Src family of non-receptor tyrosine kinases (IC50s = 2 and 6 nM for Lck and Src, respectively); used in combination with PD 0325901, CHIR99021, and SB-590885 to support self-renewal of...

WH-4-023

Reference: 9002067-5

€0.00 (tax incl.)

A selective inhibitor of the Src family of non-receptor tyrosine kinases (IC50s = 2 and 6 nM for Lck and Src, respectively); used in combination with PD 0325901, CHIR99021, and SB-590885 to support self-renewal of...

EC 23

Reference: 9002073-1

€0.00 (tax incl.)

A photostable synthetic analog of ATRA that induces differentiation in human pluripotent embryonic stem cells when used within the range of 100 nM-10 µM

EC 23

Reference: 9002073-10

€0.00 (tax incl.)

A photostable synthetic analog of ATRA that induces differentiation in human pluripotent embryonic stem cells when used within the range of 100 nM-10 µM

EC 23

Reference: 9002073-25

€0.00 (tax incl.)

A photostable synthetic analog of ATRA that induces differentiation in human pluripotent embryonic stem cells when used within the range of 100 nM-10 µM

EC 23

Reference: 9002073-5

€0.00 (tax incl.)

A photostable synthetic analog of ATRA that induces differentiation in human pluripotent embryonic stem cells when used within the range of 100 nM-10 µM

Trimethoprim-PEG-amine (trifluoroacetate salt)

Reference: 9002107-1

€0.00 (tax incl.)

A conjugated form of trimethoprim linked with polyethylene glycol (PEG) amine

Trimethoprim-PEG-amine (trifluoroacetate salt)

Reference: 9002107-10

€0.00 (tax incl.)

A conjugated form of trimethoprim linked with polyethylene glycol (PEG) amine

Trimethoprim-PEG-amine (trifluoroacetate salt)

Reference: 9002107-5

€0.00 (tax incl.)

A conjugated form of trimethoprim linked with polyethylene glycol (PEG) amine

Trimethoprim-PEG-amine (trifluoroacetate salt)

Reference: 9002107-500

€0.00 (tax incl.)

A conjugated form of trimethoprim linked with polyethylene glycol (PEG) amine

Lanicemine

Reference: 9002129-10

€0.00 (tax incl.)

A non-selective, low-trapping, voltage-dependent NMDA channel blocker (IC50 = 4-7 µM) that binds to sites within the channel pore with a Ki value of 0.56-2.1 µM; used to produce antidepressant effects without adverse...

Lanicemine

Reference: 9002129-25

€0.00 (tax incl.)

A non-selective, low-trapping, voltage-dependent NMDA channel blocker (IC50 = 4-7 µM) that binds to sites within the channel pore with a Ki value of 0.56-2.1 µM; used to produce antidepressant effects without adverse...

Lanicemine

Reference: 9002129-5

€0.00 (tax incl.)

A non-selective, low-trapping, voltage-dependent NMDA channel blocker (IC50 = 4-7 µM) that binds to sites within the channel pore with a Ki value of 0.56-2.1 µM; used to produce antidepressant effects without adverse...

Lanicemine

Reference: 9002129-50

€0.00 (tax incl.)

A non-selective, low-trapping, voltage-dependent NMDA channel blocker (IC50 = 4-7 µM) that binds to sites within the channel pore with a Ki value of 0.56-2.1 µM; used to produce antidepressant effects without adverse...

Suvorexant

Reference: 9002140-1

€0.00 (tax incl.)

A dual orexin receptor antagonist; reduces locomotor activity and promotes sleep in animal and clinical studies by inhibiting the bind of orexin A and B; decreases self-administration and seeking of cocaine in rats;...

Suvorexant

Reference: 9002140-10

€0.00 (tax incl.)

A dual orexin receptor antagonist; reduces locomotor activity and promotes sleep in animal and clinical studies by inhibiting the bind of orexin A and B; decreases self-administration and seeking of cocaine in rats;...

Suvorexant

Reference: 9002140-5

€0.00 (tax incl.)

A dual orexin receptor antagonist; reduces locomotor activity and promotes sleep in animal and clinical studies by inhibiting the bind of orexin A and B; decreases self-administration and seeking of cocaine in rats;...

Suvorexant

Reference: 9002140-50

€0.00 (tax incl.)

A dual orexin receptor antagonist; reduces locomotor activity and promotes sleep in animal and clinical studies by inhibiting the bind of orexin A and B; decreases self-administration and seeking of cocaine in rats;...