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MCHB-1 MCHB-1

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 MCHB-1

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 MCHB-1

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 AF3485

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 AF3485

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 AF3485

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 BCATc Inhibitor 2

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 BCATc Inhibitor 2

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 BCATc Inhibitor 2

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 BCATc Inhibitor 2

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 Mecillinam

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 Mecillinam

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 Mecillinam

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 Cephalexin

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 Cephalexin

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 Cephalexin

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 Cephalexin

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 Seratrodast

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 Seratrodast

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 Seratrodast

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...
Enniatin Complex Enniatin Complex

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 Enniatin Complex

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 BODIPY-aminoacetaldehyde diethyl acetal

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 BODIPY-aminoacetaldehyde diethyl acetal

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 BODIPY-aminoacetaldehyde diethyl acetal

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 BODIPY-aminoacetaldehyde diethyl acetal

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 WH-4-023

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 WH-4-023

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 WH-4-023

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 WH-4-023

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 EC 23

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 EC 23

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 EC 23

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 EC 23

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
Lanicemine Lanicemine

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 Lanicemine

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 Lanicemine

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 Lanicemine

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 Suvorexant

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 Suvorexant

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 Suvorexant

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 Suvorexant

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;...
Virginiamycin M1 Virginiamycin M1

Virginiamycin M1

Reference: 9002172-25
€0.00 (tax incl.)
A macrolide antibiotic that shows good bactericidal activity against MRSA
Virginiamycin M1 Virginiamycin M1

Virginiamycin M1

Reference: 9002172-5
€0.00 (tax incl.)
A macrolide antibiotic that shows good bactericidal activity against MRSA
Alloxan (hydrate) Alloxan (hydrate)

Alloxan (hydrate)

Reference: 9002196-10
€0.00 (tax incl.)
A toxin that selectively eliminates pancreatic β-cells in mice, rats, and certain other animals, and is used to model type 1 diabetes in humans
Alloxan (hydrate) Alloxan (hydrate)

Alloxan (hydrate)

Reference: 9002196-5
€0.00 (tax incl.)
A toxin that selectively eliminates pancreatic β-cells in mice, rats, and certain other animals, and is used to model type 1 diabetes in humans
THZ1 THZ1

THZ1

Reference: 9002215-1
€0.00 (tax incl.)
A covalent Cdk7 inhibitor (IC50s = 3.2-15.6 nM in vitro) that displays broad anti-proliferative activity against cancer cell lines, particularly T-ALL cell lines with characteristic misregulation of T cell...
THZ1 THZ1

THZ1

Reference: 9002215-10
€0.00 (tax incl.)
A covalent Cdk7 inhibitor (IC50s = 3.2-15.6 nM in vitro) that displays broad anti-proliferative activity against cancer cell lines, particularly T-ALL cell lines with characteristic misregulation of T cell...
THZ1 THZ1

THZ1

Reference: 9002215-5
€0.00 (tax incl.)
A covalent Cdk7 inhibitor (IC50s = 3.2-15.6 nM in vitro) that displays broad anti-proliferative activity against cancer cell lines, particularly T-ALL cell lines with characteristic misregulation of T cell...
THZ1 THZ1

THZ1

Reference: 9002215-500
€0.00 (tax incl.)
A covalent Cdk7 inhibitor (IC50s = 3.2-15.6 nM in vitro) that displays broad anti-proliferative activity against cancer cell lines, particularly T-ALL cell lines with characteristic misregulation of T cell...
MTSEA MTSEA

MTSEA

Reference: 9002267-10
€0.00 (tax incl.)
A positively charged sulfhydryl-specific reagent that reacts with substituted-cysteines; used to provide functional information about relative positions of amino acids within a protein and to probe binding site...
MTSEA MTSEA

MTSEA

Reference: 9002267-100
€0.00 (tax incl.)
A positively charged sulfhydryl-specific reagent that reacts with substituted-cysteines; used to provide functional information about relative positions of amino acids within a protein and to probe binding site...
MTSEA MTSEA

MTSEA

Reference: 9002267-250
€0.00 (tax incl.)
A positively charged sulfhydryl-specific reagent that reacts with substituted-cysteines; used to provide functional information about relative positions of amino acids within a protein and to probe binding site...
MTSEA MTSEA

MTSEA

Reference: 9002267-50
€0.00 (tax incl.)
A positively charged sulfhydryl-specific reagent that reacts with substituted-cysteines; used to provide functional information about relative positions of amino acids within a protein and to probe binding site...
Thromboxane B2-biotin Thromboxane B2-biotin

Thromboxane B2-biotin

Reference: 9002298-1
€0.00 (tax incl.)
An affinity probe which allows TXB2 to be detected through an interaction with the biotin ligand
Thromboxane B2-biotin Thromboxane B2-biotin

Thromboxane B2-biotin

Reference: 9002298-100
€0.00 (tax incl.)
An affinity probe which allows TXB2 to be detected through an interaction with the biotin ligand
Thromboxane B2-biotin Thromboxane B2-biotin

Thromboxane B2-biotin

Reference: 9002298-50
€0.00 (tax incl.)
An affinity probe which allows TXB2 to be detected through an interaction with the biotin ligand
Thromboxane B2-biotin Thromboxane B2-biotin

Thromboxane B2-biotin

Reference: 9002298-500
€0.00 (tax incl.)
An affinity probe which allows TXB2 to be detected through an interaction with the biotin ligand
NBD-Fructose NBD-Fructose

NBD-Fructose

Reference: 9002314-1
€0.00 (tax incl.)
A fluorescent derivative of fructose; has been used to monitor fructose uptake by the GLUT5 transporter in MCF-7, MDA-MB-435, and MDA-MB-231 human breast cancer cells; ex/em = 472/538 nm, respectively
NBD-Fructose NBD-Fructose

NBD-Fructose

Reference: 9002314-10
€0.00 (tax incl.)
A fluorescent derivative of fructose; has been used to monitor fructose uptake by the GLUT5 transporter in MCF-7, MDA-MB-435, and MDA-MB-231 human breast cancer cells; ex/em = 472/538 nm, respectively
NBD-Fructose NBD-Fructose

NBD-Fructose

Reference: 9002314-5
€0.00 (tax incl.)
A fluorescent derivative of fructose; has been used to monitor fructose uptake by the GLUT5 transporter in MCF-7, MDA-MB-435, and MDA-MB-231 human breast cancer cells; ex/em = 472/538 nm, respectively
NBD-Fructose NBD-Fructose

NBD-Fructose

Reference: 9002314-500
€0.00 (tax incl.)
A fluorescent derivative of fructose; has been used to monitor fructose uptake by the GLUT5 transporter in MCF-7, MDA-MB-435, and MDA-MB-231 human breast cancer cells; ex/em = 472/538 nm, respectively
scyllo-Inositol hexakisphosphate (sodium salt) scyllo-Inositol hexakisphosphate (sodium salt)

scyllo-Inositol hexakisphosphate (sodium salt)

Reference: 9002339-1
€0.00 (tax incl.)
A stereoisomer of IP6; identified in soil samples from Madagascar, New Zealand, and the Falkland Islands and in freshwater sediment from Danish lakes; has been used as a negative control for the stereospecific effects...
scyllo-Inositol hexakisphosphate (sodium salt) scyllo-Inositol hexakisphosphate (sodium salt)

scyllo-Inositol hexakisphosphate (sodium salt)

Reference: 9002339-10
€0.00 (tax incl.)
A stereoisomer of IP6; identified in soil samples from Madagascar, New Zealand, and the Falkland Islands and in freshwater sediment from Danish lakes; has been used as a negative control for the stereospecific effects...
scyllo-Inositol hexakisphosphate (sodium salt) scyllo-Inositol hexakisphosphate (sodium salt)

scyllo-Inositol hexakisphosphate (sodium salt)

Reference: 9002339-5
€0.00 (tax incl.)
A stereoisomer of IP6; identified in soil samples from Madagascar, New Zealand, and the Falkland Islands and in freshwater sediment from Danish lakes; has been used as a negative control for the stereospecific effects...
scyllo-Inositol hexakisphosphate (sodium salt) scyllo-Inositol hexakisphosphate (sodium salt)

scyllo-Inositol hexakisphosphate (sodium salt)

Reference: 9002339-500
€0.00 (tax incl.)
A stereoisomer of IP6; identified in soil samples from Madagascar, New Zealand, and the Falkland Islands and in freshwater sediment from Danish lakes; has been used as a negative control for the stereospecific effects...
L-Canaline L-Canaline

L-Canaline

Reference: 9002357-1
€0.00 (tax incl.)
An aminooxy analog of ornithine that irreversibly inhibits aminotransferases, including ornithine aminotransferase (Ki = 2 µM); cytotoxic to a range of organisms
L-Canaline L-Canaline

L-Canaline

Reference: 9002357-10
€0.00 (tax incl.)
An aminooxy analog of ornithine that irreversibly inhibits aminotransferases, including ornithine aminotransferase (Ki = 2 µM); cytotoxic to a range of organisms
L-Canaline L-Canaline

L-Canaline

Reference: 9002357-25
€0.00 (tax incl.)
An aminooxy analog of ornithine that irreversibly inhibits aminotransferases, including ornithine aminotransferase (Ki = 2 µM); cytotoxic to a range of organisms
L-Canaline L-Canaline

L-Canaline

Reference: 9002357-5
€0.00 (tax incl.)
An aminooxy analog of ornithine that irreversibly inhibits aminotransferases, including ornithine aminotransferase (Ki = 2 µM); cytotoxic to a range of organisms
MIV-150 MIV-150

MIV-150

Reference: 9002360-1
€0.00 (tax incl.)
A tight-binding, allosteric inhibitor of reverse transcriptase that is active against HIV-1 and HIV-2 (both EC50s = 1 nM in vitro)
MIV-150 MIV-150

MIV-150

Reference: 9002360-10
€0.00 (tax incl.)
A tight-binding, allosteric inhibitor of reverse transcriptase that is active against HIV-1 and HIV-2 (both EC50s = 1 nM in vitro)
MIV-150 MIV-150

MIV-150

Reference: 9002360-5
€0.00 (tax incl.)
A tight-binding, allosteric inhibitor of reverse transcriptase that is active against HIV-1 and HIV-2 (both EC50s = 1 nM in vitro)
MIV-150 MIV-150

MIV-150

Reference: 9002360-500
€0.00 (tax incl.)
A tight-binding, allosteric inhibitor of reverse transcriptase that is active against HIV-1 and HIV-2 (both EC50s = 1 nM in vitro)
PI-3065 PI-3065

PI-3065

Reference: 9002394-1
€0.00 (tax incl.)
A potent, selective inhibitor of p110δ (IC50 = 15 nM); suppresses tumor growth and metastasis in mouse xenograft models by inhibiting p110δ activity in regulatory T cells
PI-3065 PI-3065

PI-3065

Reference: 9002394-10
€0.00 (tax incl.)
A potent, selective inhibitor of p110δ (IC50 = 15 nM); suppresses tumor growth and metastasis in mouse xenograft models by inhibiting p110δ activity in regulatory T cells
PI-3065 PI-3065

PI-3065

Reference: 9002394-25
€0.00 (tax incl.)
A potent, selective inhibitor of p110δ (IC50 = 15 nM); suppresses tumor growth and metastasis in mouse xenograft models by inhibiting p110δ activity in regulatory T cells
PI-3065 PI-3065

PI-3065

Reference: 9002394-5
€0.00 (tax incl.)
A potent, selective inhibitor of p110δ (IC50 = 15 nM); suppresses tumor growth and metastasis in mouse xenograft models by inhibiting p110δ activity in regulatory T cells
Metronidazole Metronidazole

Metronidazole

Reference: 9002409-10
€0.00 (tax incl.)
An antibiotic; has activity against anaerobic bacteria and protozoa; reduces the growth of E. coli in vitro (MIC = 128 mg/L under anaerobic conditions); reduces viable counts of B. fragilis in a rabbit model of infection
Metronidazole Metronidazole

Metronidazole

Reference: 9002409-100
€0.00 (tax incl.)
An antibiotic; has activity against anaerobic bacteria and protozoa; reduces the growth of E. coli in vitro (MIC = 128 mg/L under anaerobic conditions); reduces viable counts of B. fragilis in a rabbit model of infection
Metronidazole Metronidazole

Metronidazole

Reference: 9002409-25
€0.00 (tax incl.)
An antibiotic; has activity against anaerobic bacteria and protozoa; reduces the growth of E. coli in vitro (MIC = 128 mg/L under anaerobic conditions); reduces viable counts of B. fragilis in a rabbit model of infection
Metronidazole Metronidazole

Metronidazole

Reference: 9002409-5
€0.00 (tax incl.)
An antibiotic; has activity against anaerobic bacteria and protozoa; reduces the growth of E. coli in vitro (MIC = 128 mg/L under anaerobic conditions); reduces viable counts of B. fragilis in a rabbit model of infection
GSK805 GSK805

GSK805

Reference: 9002444-1
€0.00 (tax incl.)
A potent, orally bioavailable RORγt inverse agonist; inhibits the expression of IL-17 (at 0.5 µM) and the development and pathogenic function of Th17 cells; reduces the severity of EAE at a daily oral dose of 10 mg/kg,
GSK805 GSK805

GSK805

Reference: 9002444-10
€0.00 (tax incl.)
A potent, orally bioavailable RORγt inverse agonist; inhibits the expression of IL-17 (at 0.5 µM) and the development and pathogenic function of Th17 cells; reduces the severity of EAE at a daily oral dose of 10 mg/kg,
GSK805 GSK805

GSK805

Reference: 9002444-5
€0.00 (tax incl.)
A potent, orally bioavailable RORγt inverse agonist; inhibits the expression of IL-17 (at 0.5 µM) and the development and pathogenic function of Th17 cells; reduces the severity of EAE at a daily oral dose of 10 mg/kg,
ZLN005 (hydrochloride) ZLN005 (hydrochloride)

ZLN005 (hydrochloride)

Reference: 9002449-10
€0.00 (tax incl.)
A small molecule that stimulates the expression of PGC-1α and downstream genes in skeletal muscle cells, improving glucose utilization and fatty acid oxidation at a concentration of 20 μM; 15 mg/kg/day administered to...
ZLN005 (hydrochloride) ZLN005 (hydrochloride)

ZLN005 (hydrochloride)

Reference: 9002449-25
€0.00 (tax incl.)
A small molecule that stimulates the expression of PGC-1α and downstream genes in skeletal muscle cells, improving glucose utilization and fatty acid oxidation at a concentration of 20 μM; 15 mg/kg/day administered to...
ZLN005 (hydrochloride) ZLN005 (hydrochloride)

ZLN005 (hydrochloride)

Reference: 9002449-5
€0.00 (tax incl.)
A small molecule that stimulates the expression of PGC-1α and downstream genes in skeletal muscle cells, improving glucose utilization and fatty acid oxidation at a concentration of 20 μM; 15 mg/kg/day administered to...
ZLN005 (hydrochloride) ZLN005 (hydrochloride)

ZLN005 (hydrochloride)

Reference: 9002449-50
€0.00 (tax incl.)
A small molecule that stimulates the expression of PGC-1α and downstream genes in skeletal muscle cells, improving glucose utilization and fatty acid oxidation at a concentration of 20 μM; 15 mg/kg/day administered to...
Myristoleic Acid Myristoleic Acid

Myristoleic Acid

Reference: 9002461-100
€0.00 (tax incl.)
A bioactive fatty acid; induces apoptosis and necrosis in human prostate cancer LNCaP cells at a rate of 8.8% and 8.1%, respectively; inhibits C. albicans germination (MIC = 9 µM); inhibits osteogenesis in vitro via...
Myristoleic Acid Myristoleic Acid

Myristoleic Acid

Reference: 9002461-250
€0.00 (tax incl.)
A bioactive fatty acid; induces apoptosis and necrosis in human prostate cancer LNCaP cells at a rate of 8.8% and 8.1%, respectively; inhibits C. albicans germination (MIC = 9 µM); inhibits osteogenesis in vitro via...

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