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Reference: CDX-G0198-M010
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10-Gingerol is originally found in species of Zingiber. It exhibits antiemetic, anticancer, antioxidative, anti-inflammatory and antibiotic activities. 10-Gingerol increases radical scavenging of superoxide and...
Reference: CDX-G0198-M005
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10-Gingerol is originally found in species of Zingiber. It exhibits antiemetic, anticancer, antioxidative, anti-inflammatory and antibiotic activities. 10-Gingerol increases radical scavenging of superoxide and...
Reference: SYN-1099-M100
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ZSTK474 Inhibits all four PI3K isoforms in an ATP-competitive manner. IC(50) is approximately 37nM.
Reference: SYN-1099-M050
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ZSTK474 Inhibits all four PI3K isoforms in an ATP-competitive manner. IC(50) is approximately 37nM.
Reference: SYN-1099-M010
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ZSTK474 Inhibits all four PI3K isoforms in an ATP-competitive manner. IC(50) is approximately 37nM.
Reference: SYN-1099-M005
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ZSTK474 Inhibits all four PI3K isoforms in an ATP-competitive manner. IC(50) is approximately 37nM.
Reference: SYN-1099-M001
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ZSTK474 Inhibits all four PI3K isoforms in an ATP-competitive manner. IC(50) is approximately 37nM.
Reference: CDX-Z0015-M500
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Fungicide. Primarily an oomycete fungicide although it has some activity against ascomycetes and basidiomycetes. The product acts by disruption of the microtubule structure and inhibition of cell division. The...
Reference: CDX-Z0015-M100
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Fungicide. Primarily an oomycete fungicide although it has some activity against ascomycetes and basidiomycetes. The product acts by disruption of the microtubule structure and inhibition of cell division. The...
Reference: CDX-Z0510-M001
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ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1,...
Reference: CDX-Z0512-M001
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For application to living cells, the diacetyl derivative of ZnAF-2F, ZnAF-2F DA, was synthesized. ZnAF-2F DA can permeate through the cell membrane, and is hydrolyzed by esterase in the cytosol to yield ZnAF-2F, which...
Reference: CDX-Z0012-M005
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For application to living cells, the diacetyl derivative of ZnAF-2F, ZnAF-2F DA, was synthesized. ZnAF-2F DA can permeate through the cell membrane, and is hydrolyzed by esterase in the cytosol to yield ZnAF-2F, which...
Reference: CDX-Z0012-M001
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For application to living cells, the diacetyl derivative of ZnAF-2F, ZnAF-2F DA, was synthesized. ZnAF-2F DA can permeate through the cell membrane, and is hydrolyzed by esterase in the cytosol to yield ZnAF-2F, which...
Reference: CDX-Z0010-M025
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ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1,...
Reference: CDX-Z0010-M005
€0.00 (tax incl.)
ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1,...
Reference: CDX-Z0010-M001
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ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1,...
Reference: CDX-Z0506-M001
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A membrane-impermeable ethylenediaminofluoresceinyl compound that acts as a high-affinity Zn2+-specific fluorescent probe (Kd = 2.7 nM). It shows low basal fluorescence and the fluorescence intensity increases...
Reference: CDX-Z0508-M001
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Suitable for the fluorimetric detection of Zn2+ (after esterase hydrolysis). Spectral data: lambdaex 492nm; lambdaem 515nm in PBS.
Reference: CDX-Z0008-M005
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Suitable for the fluorimetric detection of Zn2+ (after esterase hydrolysis). Spectral data: lambdaex 492nm; lambdaem 515nm in PBS.
Reference: CDX-Z0008-M001
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Suitable for the fluorimetric detection of Zn2+ (after esterase hydrolysis). Spectral data: lambdaex 492nm; lambdaem 515nm in PBS.
Reference: CDX-Z0006-M025
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A membrane-impermeable ethylenediaminofluoresceinyl compound that acts as a high-affinity Zn2+-specific fluorescent probe (Kd = 2.7 nM). It shows low basal fluorescence and the fluorescence intensity increases...
Reference: CDX-Z0006-M005
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A membrane-impermeable ethylenediaminofluoresceinyl compound that acts as a high-affinity Zn2+-specific fluorescent probe (Kd = 2.7 nM). It shows low basal fluorescence and the fluorescence intensity increases...
Reference: CDX-Z0006-M001
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A membrane-impermeable ethylenediaminofluoresceinyl compound that acts as a high-affinity Zn2+-specific fluorescent probe (Kd = 2.7 nM). It shows low basal fluorescence and the fluorescence intensity increases...
Reference: CDX-Z0509-M001
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ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1,...
Reference: CDX-Z0511-M001
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For application to living cells, the diacetyl derivative of ZnAF-1F, ZnAF-1F DA, was synthesized. ZnAF-1F DA can permeate through the cell membrane, and is hydrolyzed by esterase in the cytosol to yield ZnAF-1F, which...
Reference: CDX-Z0011-M005
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For application to living cells, the diacetyl derivative of ZnAF-1F, ZnAF-1F DA, was synthesized. ZnAF-1F DA can permeate through the cell membrane, and is hydrolyzed by esterase in the cytosol to yield ZnAF-1F, which...
Reference: CDX-Z0011-M001
€0.00 (tax incl.)
For application to living cells, the diacetyl derivative of ZnAF-1F, ZnAF-1F DA, was synthesized. ZnAF-1F DA can permeate through the cell membrane, and is hydrolyzed by esterase in the cytosol to yield ZnAF-1F, which...
Reference: CDX-Z0009-M025
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ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1,...
Reference: CDX-Z0009-M005
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ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1,...
Reference: CDX-Z0009-M001
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ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1,...
Reference: CDX-Z0505-M001
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A membrane-impermeable ethylenediaminofluoresceinyl compound that acts as a high-affinity Zn2+-specific fluorescent probe. Spectral data: lambdaex 492 nm; lambdaem 514 nm in PBS.
Reference: CDX-Z0507-M001
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Suitable for the fluorimetric detection of Zn2+ (after esterase hydrolysis). Spectral data: lambdaex 492nm; lambdaem 515nm in PBS.
Reference: CDX-Z0007-M025
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Suitable for the fluorimetric detection of Zn2+ (after esterase hydrolysis). Spectral data: lambdaex 492nm; lambdaem 515nm in PBS.
Reference: CDX-Z0007-M005
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Suitable for the fluorimetric detection of Zn2+ (after esterase hydrolysis). Spectral data: lambdaex 492nm; lambdaem 515nm in PBS.
Reference: CDX-Z0007-M001
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Suitable for the fluorimetric detection of Zn2+ (after esterase hydrolysis). Spectral data: lambdaex 492nm; lambdaem 515nm in PBS.
Reference: CDX-Z0005-M125
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A membrane-impermeable ethylenediaminofluoresceinyl compound that acts as a high-affinity Zn2+-specific fluorescent probe. Spectral data: lambdaex 492 nm; lambdaem 514 nm in PBS.
Reference: CDX-Z0005-M005
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A membrane-impermeable ethylenediaminofluoresceinyl compound that acts as a high-affinity Zn2+-specific fluorescent probe. Spectral data: lambdaex 492 nm; lambdaem 514 nm in PBS.
Reference: AG-40T-0103-C050
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M13 endopeptidases are single-pass, transmembrane zinc-metallopeptidases responsible in human for the regulation of the biological activity of many hormones and peptides and are involved in many important processes...
Reference: CDX-Z0013-M050
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Zinc(II) specific fluorophores probes.
Reference: CDX-Z0013-M005
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Zinc(II) specific fluorophores probes.
Reference: CDX-Z0013-M001
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Zinc(II) specific fluorophores probes.
Reference: CDX-Z0014-M025
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Used to detect zinc in cells by UV fluorescence.
Reference: CDX-Z0014-M005
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Used to detect zinc in cells by UV fluorescence.
Reference: CDX-Z0014-M001
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Used to detect zinc in cells by UV fluorescence.
Reference: CDX-Z0001-M125
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Membrane permeable fluorophore suitable for the fluorometric detection of Zn2+. In living cells Zinpyr-1 mainly stains the Golgi or a Golgi-associated vesicle.
Reference: CDX-Z0001-M020
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Membrane permeable fluorophore suitable for the fluorometric detection of Zn2+. In living cells Zinpyr-1 mainly stains the Golgi or a Golgi-associated vesicle.
Reference: CDX-Z0028-G005
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A colorimetric reagent for Zn, Cu and Hg detection and a metal indicator in EDTA titration. The aqueous solution of Zincon is yellow or orange-yellow in weak alkaline conditions, and turns blue in the presence of Cu...
Reference: CDX-Z0028-G001
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A colorimetric reagent for Zn, Cu and Hg detection and a metal indicator in EDTA titration. The aqueous solution of Zincon is yellow or orange-yellow in weak alkaline conditions, and turns blue in the presence of Cu...
Reference: AG-48B-1000-KI01
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This assay is a less than 1 hour sandwich Enzyme Linked-Immunosorbent Assay (ELISA) for quantitative determination of human Zinc-alpha-2-glycoprotein in biological fluids. Zinc-alpha-2-glycoprotein (ZAG) was first...
Reference: AG-46B-0008-KI01
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Zinc-alpha-2-glycoprotein (ZAG), first identified in the 1960s, derives its name from its precipitation from human plasma upon the addition of zinc salts. ZAG has since been found in secretory epithelial cells and in...
Reference: AG-40B-0146-3050
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Zinc-alpha-2-glycoprotein (ZAG), first identified in the 1960s, derives its name from its precipitation from human plasma upon the addition of zinc salts. ZAG has since been found in secretory epithelial cells and in...
Reference: AG-40B-0146-C050
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Zinc-alpha-2-glycoprotein (ZAG), first identified in the 1960s, derives its name from its precipitation from human plasma upon the addition of zinc salts. ZAG has since been found in secretory epithelial cells and in...
Reference: AG-40B-0146-C010
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Zinc-alpha-2-glycoprotein (ZAG), first identified in the 1960s, derives its name from its precipitation from human plasma upon the addition of zinc salts. ZAG has since been found in secretory epithelial cells and in...
Reference: JAI-CZN-001
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Zinc (Zn2+) is an essential trace element, vital for the health of animals, plants, and microorganisms . Zinc is found in hundreds of enzymes, is stored and transferred in metallothioneins, and serves as structural...
Reference: CDX-F0019-M001
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Zin3 AM is a cell-permeable Zn2+-selective indicator (Absorption=456nm), that once it enters the cell is hydrolized by esterases to convert the bright fluorescent Zin3 (Ex/Em: ~494/516nm). Zin3 is suitable for...
Reference: CDX-F0019-C500
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Zin3 AM is a cell-permeable Zn2+-selective indicator (Absorption=456nm), that once it enters the cell is hydrolized by esterases to convert the bright fluorescent Zin3 (Ex/Em: ~494/516nm). Zin3 is suitable for...
Reference: CDX-F0019-C100
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Zin3 AM is a cell-permeable Zn2+-selective indicator (Absorption=456nm), that once it enters the cell is hydrolized by esterases to convert the bright fluorescent Zin3 (Ex/Em: ~494/516nm). Zin3 is suitable for...
Reference: CDX-Z0025-M010
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Synthetic beta2-adrenoreceptor agonist that binds with the muscle beta-adrenoreceptors, leading to the activation of protein kinase A, an enzyme responsible for changes in protein synthesis and degradation, in...
Reference: CDX-Z0025-M005
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Synthetic beta2-adrenoreceptor agonist that binds with the muscle beta-adrenoreceptors, leading to the activation of protein kinase A, an enzyme responsible for changes in protein synthesis and degradation, in...
Reference: AG-CN2-0004-M050
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Chemopreventive probe. Apoptosis inducer. Potent anti-tumor compound. Anti-inflammatory activity by downregulating COX-2 and iNOS expression via modulation of NF-kappaB activation. Antinociceptive. Probe to study...
Reference: AG-CN2-0004-M010
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Chemopreventive probe. Apoptosis inducer. Potent anti-tumor compound. Anti-inflammatory activity by downregulating COX-2 and iNOS expression via modulation of NF-kappaB activation. Antinociceptive. Probe to study...
Reference: AG-CN2-0128-M001
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Cyclic peptide antibiotic Antibacterial.
Reference: AG-CN2-0128-C250
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Cyclic peptide antibiotic Antibacterial.
Reference: BVT-0394-M005
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Resorcylic acid lactone. Mycotoxin. Regulator of fungal morphogenesis. Mycoestrogen with anabolic and uterotrophic activity. Ecdysteroid antagonist. Gonadotropin inhibitor. Interleukin antagonist. Apoptosis inducer....
Reference: AG-CP3-0008-M001
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Selective cell permeable and irreversible MALT1 inhibitor. Inhibits NF-kappaB-dependent gene expression and affects the growth, proliferation and survival of activated B cell-like diffuse large B cell lymphomas...
Reference: AG-CP3-0008-C500
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Selective cell permeable and irreversible MALT1 inhibitor. Inhibits NF-kappaB-dependent gene expression and affects the growth, proliferation and survival of activated B cell-like diffuse large B cell lymphomas...
Reference: AG-CP3-0027-M025
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Proteasome subunit alpha type-1 (Macropain) substrate used for assaying the trypsin-like activity of the 20S proteasome. Cysteine proteinase falcipain-2 and falcipain-3 (malarial hemoglobinases) substrate. Cathepsin S...
Reference: AG-CP3-0027-M005
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Proteasome subunit alpha type-1 (Macropain) substrate used for assaying the trypsin-like activity of the 20S proteasome. Cysteine proteinase falcipain-2 and falcipain-3 (malarial hemoglobinases) substrate. Cathepsin S...
Reference: AG-CP3-0002-M005
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Cell permeable, non-selective broad-spectrum caspase inhibitor. Binds irreversibly to the catalytic site of caspase proteases. The peptide is O-methylated in the P1 position on aspartic acid, providing enhanced...
Reference: AG-CP3-0002-M001
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Cell permeable, non-selective broad-spectrum caspase inhibitor. Binds irreversibly to the catalytic site of caspase proteases. The peptide is O-methylated in the P1 position on aspartic acid, providing enhanced...
Reference: AG-CP3-0028-M025
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Fluorogenic substrate, specifically used to determine the enzyme activity of Cathepsin L. Useful for the study of cathepsin activity and for screening small molecule inhibitors for drug discovery and HTS...
Reference: AG-CP3-0028-M005
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Fluorogenic substrate, specifically used to determine the enzyme activity of Cathepsin L. Useful for the study of cathepsin activity and for screening small molecule inhibitors for drug discovery and HTS...
Reference: AG-CP3-0021-M005
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Reversible and cell permeable proteasome inhibitor. Specifically inhibits the chymotrypsin-like activity of the proteasome. Calpain and cathepsin inhibitor. Does not inhibit the peptidyl-glutamyl peptide hydrolyzing...
Reference: AG-CP3-0021-M001
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Reversible and cell permeable proteasome inhibitor. Specifically inhibits the chymotrypsin-like activity of the proteasome. Calpain and cathepsin inhibitor. Does not inhibit the peptidyl-glutamyl peptide hydrolyzing...
Reference: AG-CP3-0015-M005
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Potent, reversible and cell permeable proteasome inhibitor. Specifically inhibits the chymotrypsin-like activity of the proteasome. Calpain and cathepsin inhibitor. Apoptosis inducer in Rat-1 and PC12 cells via a...
Reference: AG-CP3-0015-M001
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Potent, reversible and cell permeable proteasome inhibitor. Specifically inhibits the chymotrypsin-like activity of the proteasome. Calpain and cathepsin inhibitor. Apoptosis inducer in Rat-1 and PC12 cells via a...
Reference: AG-CP3-0011-M025
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Potent, cell permeable and selective, reversible proteasome inhibitor. Blocks degradation of short-lived proteins and induces a heat shock response. NF-kappaB activation inhibitor through IkappaB degradation. Cell...
Reference: AG-CP3-0011-M005
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Potent, cell permeable and selective, reversible proteasome inhibitor. Blocks degradation of short-lived proteins and induces a heat shock response. NF-kappaB activation inhibitor through IkappaB degradation. Cell...
Reference: AG-CP3-0011-M001
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Potent, cell permeable and selective, reversible proteasome inhibitor. Blocks degradation of short-lived proteins and induces a heat shock response. NF-kappaB activation inhibitor through IkappaB degradation. Cell...
Reference: AG-CP3-0024-M005
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Highly potent and selective cell permeable inhibitor of the proteasome. Inhibits the chymotrypsin-like and caspase-like peptidase activity of the proteasome. Calpain and cathepsin inhibitor. Autophagy activator....
Reference: AG-CP3-0024-M001
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Highly potent and selective cell permeable inhibitor of the proteasome. Inhibits the chymotrypsin-like and caspase-like peptidase activity of the proteasome. Calpain and cathepsin inhibitor. Autophagy activator....
Reference: AG-CP3-0024-C200
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Highly potent and selective cell permeable inhibitor of the proteasome. Inhibits the chymotrypsin-like and caspase-like peptidase activity of the proteasome. Calpain and cathepsin inhibitor. Autophagy activator....
Reference: AG-CP3-0019-M005
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Fluorogenic substrate for measuring the chymotrypsin-like peptidase activity of the 20S proteasome. Excitation: 345nm. Emission: 445nm. This substrate is useful for inhibitor screening and kinetic analysis.
Reference: AG-CP3-0019-M001
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Fluorogenic substrate for measuring the chymotrypsin-like peptidase activity of the 20S proteasome. Excitation: 345nm. Emission: 445nm. This substrate is useful for inhibitor screening and kinetic analysis.
Reference: SBB-PS0006-M002
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Z-LLE-AMC is a fluorogenic peptide substrate for measuring caspase-like activity of the proteasome. Hydrolysis of this substrate by the beta1-subunit of the 20S proteasome is monitored by observing fluorescence at an...
Reference: AG-CP3-0022-M005
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Fluorogenic substrate for the peptidylglutamyl-peptide hydrolysing (PGPH) (caspase-like) activity of the 20S proteasome. Excitation: 380nm. Emission: 460nm.
Reference: AG-CP3-0022-M001
€0.00 (tax incl.)
Fluorogenic substrate for the peptidylglutamyl-peptide hydrolysing (PGPH) (caspase-like) activity of the 20S proteasome. Excitation: 380nm. Emission: 460nm.
Reference: AG-CP3-0023-M005
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Fluorogenic tetrapeptide substrate for ubiquitin C-terminal hydrolases (UCHs, e.g. UCHL3) and isopeptidase T. LRGG is the preferred substrate sequence of the human deSUMOylating enzymes SENP6 and SENP7. Excitation:...
Reference: AG-CP3-0023-M001
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Fluorogenic tetrapeptide substrate for ubiquitin C-terminal hydrolases (UCHs, e.g. UCHL3) and isopeptidase T. LRGG is the preferred substrate sequence of the human deSUMOylating enzymes SENP6 and SENP7. Excitation:...
Reference: CDX-Y0013-G025
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alpha2-Adrenoceptor antagonist. pKi values are 8.52, 8.00 and 9.17 for human alpha2A, alpha2B and alpha2C receptors, respectively.
Reference: CDX-Y0013-G005
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alpha2-Adrenoceptor antagonist. pKi values are 8.52, 8.00 and 9.17 for human alpha2A, alpha2B and alpha2C receptors, respectively.
Reference: SYN-1094-M100
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YM-201636 is a cell-permeable and selective inhibitor of PIKfyve (IC(50) of 33nM). It disrupts retroviral budding from cells, apparently by interfering with the endosomal sorting complex required for transport (ESCRT)...
Reference: SYN-1094-M050
€0.00 (tax incl.)
YM-201636 is a cell-permeable and selective inhibitor of PIKfyve (IC(50) of 33nM). It disrupts retroviral budding from cells, apparently by interfering with the endosomal sorting complex required for transport (ESCRT)...
Reference: SYN-1094-M010
€0.00 (tax incl.)
YM-201636 is a cell-permeable and selective inhibitor of PIKfyve (IC(50) of 33nM). It disrupts retroviral budding from cells, apparently by interfering with the endosomal sorting complex required for transport (ESCRT)...
Reference: SYN-1094-M005
€0.00 (tax incl.)
YM-201636 is a cell-permeable and selective inhibitor of PIKfyve (IC(50) of 33nM). It disrupts retroviral budding from cells, apparently by interfering with the endosomal sorting complex required for transport (ESCRT)...
Reference: SYN-1094-M001
€0.00 (tax incl.)
YM-201636 is a cell-permeable and selective inhibitor of PIKfyve (IC(50) of 33nM). It disrupts retroviral budding from cells, apparently by interfering with the endosomal sorting complex required for transport (ESCRT)...

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