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Enzo Life Sciences

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Catalogue No. Type Brand Name Description Size Availability Unit
Price (S$)
Order Qty
ALX-350-312-M025 Biochemical Enzo Life Sciences (-)-Arctigenin Lignan derivative, which shows antitumor, anti-inflammatory, immunomodulatory and neuroprotective activities. Down-regulates anti-apoptotic protein Bcl-XL. Potent inhibitor of HIV type-I integrase and DNA topoisomerase II. Shows phytoestrogenic and cytotoxic properties against Hep62 cells.  Antagonist for platelet activating factor and Ca2+. Blocks the activation of Akt (protein kinase B; PKB) induced by glucose starvation. 25 mg
4-6 weeks - Log In
ALX-350-318-M025 Biochemical Enzo Life Sciences (-)-Arctiin Lignan derivative with antitumor activities. Down-regulates anti-apoptotic protein Bcl-XL. Potent inhibitor of HIV type-I integrase and DNA topoisomerase II. Shows phytoestrogenic activity and is an antagonist for platelet activating factor and Ca2+. 25 mg
4-6 weeks - Log In
BML-EA149-0050 Biochemical Enzo Life Sciences (-)-Bicuculline methiodide A water soluble analog of bicuculline, the classic GABAA antagonist. 50 mg
4-6 weeks - Log In
ALX-350-216-M100 Biochemical Enzo Life Sciences (-)-Eburnamonine Cerebral metabolic stimulant; shows antihypoxic effects. Vasodilator. 100 mg
4-6 weeks - Log In
ALX-270-263-M050 Biochemical Enzo Life Sciences (-)-Epigallocatechin gallate Antitumor reagent. Antioxidant. Protects cells from lipid peroxidation and DNA damage induced by reactive free radicals. Inhibits inducible nitric oxide synthase (iNOS; NOS II). Chemopreventive anticancer agent. Induces apoptosis in human cancer cell lines. Inhibits MAP kinase mediated signalling pathways. Inhibits angiogenesis. Inhibits telomerase and DNA methyltransferase. Anti-inflammatory agent. 50 mg
4-6 weeks - Log In
ALX-270-263-M010 Biochemical Enzo Life Sciences (-)-Epigallocatechin gallate Antitumor reagent. Antioxidant. Protects cells from lipid peroxidation and DNA damage induced by reactive free radicals. Inhibits inducible nitric oxide synthase (iNOS; NOS II). Chemopreventive anticancer agent. Induces apoptosis in human cancer cell lines. Inhibits MAP kinase mediated signalling pathways. Inhibits angiogenesis. Inhibits telomerase and DNA methyltransferase. Anti-inflammatory agent. 10 mg
4-6 weeks - Log In
ALX-550-065-MC05 Biochemical Enzo Life Sciences (-)-Huperzine A Plant alkaloid. Neurotoxin. Potent acetylcholinesterase inhibitor. Active isomer with acetylcholine esterase activity. Protects cells against hydrogen peroxide, β-amyloid, glutamate, ischemia and staurosporine-induced cytotoxicity and apoptosis. Prospective agent for the treatment of Alzheimer's disease. For the racemic modification, see (±)-Huperzine A (Prod. No. ALX-550-064). 0.5 mg
4-6 weeks - Log In
ALX-550-065-M001 Biochemical Enzo Life Sciences (-)-Huperzine A Plant alkaloid. Neurotoxin. Potent acetylcholinesterase inhibitor. Active isomer with acetylcholine esterase activity. Protects cells against hydrogen peroxide, β-amyloid, glutamate, ischemia and staurosporine-induced cytotoxicity and apoptosis. Prospective agent for the treatment of Alzheimer's disease. For the racemic modification, see (±)-Huperzine A (Prod. No. ALX-550-064). 1 mg
4-6 weeks - Log In
ALX-420-011-C300 Biochemical Enzo Life Sciences (-)-Indolactam V Moderately potent indolactam activator of protein kinase C (PKC). Increases cytoplasmic mRNAs. Exhibits tumor promoting activity. Directs differentiation of human embryonic stem cells to pancreatic progenitor cells. 300 µg
4-6 weeks - Log In
ALX-350-402-M002 Biochemical Enzo Life Sciences (-)-Matairesinol Phytoestrogen. Inhibits P-glycoprotein. 2 mg
4-6 weeks - Log In
ALX-420-042-M100 Biochemical Enzo Life Sciences (-)-Menthol Cooling agent. Strongly activates TRPM8 (cold menthol receptor 1; CMR1) and TRPA1. 100 mg
4-6 weeks - Log In
ALX-430-025-M005 Biochemical Enzo Life Sciences (-)-p-Bromotetramisole . oxalate Potent alkaline phosphatase inhibitor. Mimics the action of orthovanadate in the potentiation of fluorouracil antiproliferative activity. Cell permeable.  5 mg
4-6 weeks - Log In
BML-D109-0005 Biochemical Enzo Life Sciences (-)-Quinpirole . HCl Selective dopamine D2 receptor agonist. 5 mg
4-6 weeks - Log In
BML-D109-0025 Biochemical Enzo Life Sciences (-)-Quinpirole . HCl Selective dopamine D2 receptor agonist. 25 mg
4-6 weeks - Log In
BML-UW0620-0025 Protein Enzo Life Sciences ([K11-only]Ub)n-ubiquitinylated substrate - 25 µg
4-6 weeks - Log In
BML-UW0625-0025 Protein Enzo Life Sciences ([K27-only]Ub)n-ubiquitinylated substrate - 25 µg
4-6 weeks - Log In
BML-UW0630-0025 Protein Enzo Life Sciences ([K29-only]Ub)n-ubiquitinylated substrate - 25 µg
4-6 weeks - Log In
BML-UW0635-0025 Protein Enzo Life Sciences ([K33-only]Ub)n-ubiquitinylated substrate - 25 µg
4-6 weeks - Log In
BML-UW0640-0025 Protein Enzo Life Sciences ([K48-only]Ub)n-ubiquitinylated substrate - 25 µg
4-6 weeks - Log In
BML-UW0615-0025 Protein Enzo Life Sciences ([K6-only]Ub)n-ubiquitinylated substrate - 25 µg
4-6 weeks - Log In
BML-UW0645-0025 Protein Enzo Life Sciences ([K63-only]Ub)n-ubiquitinylated substrate - 25 µg
4-6 weeks - Log In
BML-CC101-0001 Biochemical Enzo Life Sciences (+)-Aphidicolin Produced by Cephalosporium aphidicola and other fungi. A diterpene fungal metabolite that acts as reversible inhibitor of eukaryotic nuclear DNA replication. Useful for cell synchronization. Blocks the cell cycle at early S phase. Prolongs the half life of DNA methyltransferase. Specific inhibitor of DNA polymerase α and δ in eukaryotic cells and in some viruses of animal origin. Acts synergistically with vincristine and doxorubicin. Apoptosis inhibitor/inducer. 1 mg
4-6 weeks - Log In
ALX-550-515-M250 Biochemical Enzo Life Sciences (+)-Bicuculline GABAA receptor antagonist. 250 mg
4-6 weeks - Log In
ALX-550-515-M050 Biochemical Enzo Life Sciences (+)-Bicuculline GABAA receptor antagonist. 50 mg
4-6 weeks - Log In
(-)-Arctigenin

Description

Lignan derivative, which shows antitumor, anti-inflammatory, immunomodulatory and neuroprotective activities. Down-regulates anti-apoptotic protein Bcl-XL. Potent inhibitor of HIV type-I integrase and DNA topoisomerase II. Shows phytoestrogenic and cytotoxic properties against Hep62 cells.  Antagonist for platelet activating factor and Ca2+. Blocks the activation of Akt (protein kinase B; PKB) induced by glucose starvation.

$ 230.00

 

(-)-Arctiin

Description

Lignan derivative with antitumor activities. Down-regulates anti-apoptotic protein Bcl-XL. Potent inhibitor of HIV type-I integrase and DNA topoisomerase II. Shows phytoestrogenic activity and is an antagonist for platelet activating factor and Ca2+.

$ 180.00

 

(-)-Bicuculline methiodide

Description

A water soluble analog of bicuculline, the classic GABAA antagonist.

$ 370.00

 

(-)-Eburnamonine

Description

Cerebral metabolic stimulant; shows antihypoxic effects. Vasodilator.

$ 260.00

 

(-)-Epigallocatechin gallate

Description

Antitumor reagent. Antioxidant. Protects cells from lipid peroxidation and DNA damage induced by reactive free radicals. Inhibits inducible nitric oxide synthase (iNOS; NOS II). Chemopreventive anticancer agent. Induces apoptosis in human cancer cell lines. Inhibits MAP kinase mediated signalling pathways. Inhibits angiogenesis. Inhibits telomerase and DNA methyltransferase. Anti-inflammatory agent.

$ 180.00

 

(-)-Epigallocatechin gallate

Description

Antitumor reagent. Antioxidant. Protects cells from lipid peroxidation and DNA damage induced by reactive free radicals. Inhibits inducible nitric oxide synthase (iNOS; NOS II). Chemopreventive anticancer agent. Induces apoptosis in human cancer cell lines. Inhibits MAP kinase mediated signalling pathways. Inhibits angiogenesis. Inhibits telomerase and DNA methyltransferase. Anti-inflammatory agent.

$ 140.00

 

(-)-Huperzine A

Description

Plant alkaloid. Neurotoxin. Potent acetylcholinesterase inhibitor. Active isomer with acetylcholine esterase activity. Protects cells against hydrogen peroxide, β-amyloid, glutamate, ischemia and staurosporine-induced cytotoxicity and apoptosis. Prospective agent for the treatment of Alzheimer's disease. For the racemic modification, see (±)-Huperzine A (Prod. No. ALX-550-064).

$ 130.00

 

(-)-Huperzine A

Description

Plant alkaloid. Neurotoxin. Potent acetylcholinesterase inhibitor. Active isomer with acetylcholine esterase activity. Protects cells against hydrogen peroxide, β-amyloid, glutamate, ischemia and staurosporine-induced cytotoxicity and apoptosis. Prospective agent for the treatment of Alzheimer's disease. For the racemic modification, see (±)-Huperzine A (Prod. No. ALX-550-064).

$ 190.00

 

(-)-Indolactam V

Description

Moderately potent indolactam activator of protein kinase C (PKC). Increases cytoplasmic mRNAs. Exhibits tumor promoting activity. Directs differentiation of human embryonic stem cells to pancreatic progenitor cells.

$ 460.00

 

(-)-Matairesinol

Description

Phytoestrogen. Inhibits P-glycoprotein.

$ 210.00

 

(-)-Menthol

Description

Cooling agent. Strongly activates TRPM8 (cold menthol receptor 1; CMR1) and TRPA1.

$ 210.00

 

(-)-p-Bromotetramisole . oxalate

Description

Potent alkaline phosphatase inhibitor. Mimics the action of orthovanadate in the potentiation of fluorouracil antiproliferative activity. Cell permeable. 

$ 180.00

 

(-)-Quinpirole . HCl

Description

Selective dopamine D2 receptor agonist.

$ 310.00

 

(-)-Quinpirole . HCl

Description

Selective dopamine D2 receptor agonist.

$ 1,280.00

 

([K11-only]Ub)n-ubiquitinylated substrate

Description

$ 610.00

 

([K27-only]Ub)n-ubiquitinylated substrate

Description

$ 600.00

 

([K29-only]Ub)n-ubiquitinylated substrate

Description

$ 600.00

 

([K33-only]Ub)n-ubiquitinylated substrate

Description

$ 600.00

 

([K48-only]Ub)n-ubiquitinylated substrate

Description

$ 640.00

 

([K6-only]Ub)n-ubiquitinylated substrate

Description

$ 600.00

 

([K63-only]Ub)n-ubiquitinylated substrate

Description

$ 610.00

 

(+)-Aphidicolin

Description

Produced by Cephalosporium aphidicola and other fungi. A diterpene fungal metabolite that acts as reversible inhibitor of eukaryotic nuclear DNA replication. Useful for cell synchronization. Blocks the cell cycle at early S phase. Prolongs the half life of DNA methyltransferase. Specific inhibitor of DNA polymerase α and δ in eukaryotic cells and in some viruses of animal origin. Acts synergistically with vincristine and doxorubicin. Apoptosis inhibitor/inducer.

$ 220.00

 

(+)-Bicuculline

Description

GABAA receptor antagonist.

$ 520.00

 

(+)-Bicuculline

Description

GABAA receptor antagonist.

$ 170.00