Category: Reagents

Reference: AG-CN2-0318-M001
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Glycolipodepsipeptide antibiotic. Complex of structurally related molecules A1, A2 and A3, with ramoplanin A2 as the primary component. Antibacterial and antiviral agent with activity against aerobic and anaerobic...
Reference: AG-CN2-0318-M005
€0.00 (tax incl.)
Glycolipodepsipeptide antibiotic. Complex of structurally related molecules A1, A2 and A3, with ramoplanin A2 as the primary component. Antibacterial and antiviral agent with activity against aerobic and anaerobic...
Reference: AG-CN2-0320-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0320-M050
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Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0321-G001
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Ansamycin antibiotic. Intermediate of rifampicin. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and...
Reference: AG-CN2-0321-G005
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Ansamycin antibiotic. Intermediate of rifampicin. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and...
Reference: AG-CN2-0321-G010
€0.00 (tax incl.)
Ansamycin antibiotic. Intermediate of rifampicin. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and...
Reference: AG-CN2-0322-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0322-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0323-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0323-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0324-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0324-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0325-M010
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Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0325-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0326-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0326-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0327-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0327-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0328-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Intermediate of rifampicin. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and...
Reference: AG-CN2-0328-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Intermediate of rifampicin. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and...
Reference: AG-CN2-0329-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0329-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0330-M010
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Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0330-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0331-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0331-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0332-M010
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Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0332-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0333-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0333-M500
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Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0334-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0334-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0335-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0335-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0336-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Potent inhibitor of nucleic acid polymerizing enzymes and of some hormone receptors. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Inhibitor of RNA-dependent DNA...
Reference: AG-CN2-0336-M050
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Ansamycin antibiotic. Potent inhibitor of nucleic acid polymerizing enzymes and of some hormone receptors. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Inhibitor of RNA-dependent DNA...
Reference: AG-CN2-0337-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0337-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP). Effective against mycobacteria, and are therefore used in research of tuberculosis, leprosy and mycobacterium avium complex...
Reference: AG-CN2-0338-M010
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0338-M050
€0.00 (tax incl.)
Ansamycin antibiotic. Hydrazone of 3-formylrifamycin SV. Selective inhibitor of bacterial DNA-dependent RNA polymerase (RNAP).
Reference: AG-CN2-0339-M001
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Anthracene antibiotic. Antibacterial agent. Active against both Gram-positive and Gram-negative bacteria. Inhibits the initiation stage of bacterial protein synthesis by binding to the inter-subunit bridge B2a on the...
Reference: AG-CN2-0339-M005
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Anthracene antibiotic. Antibacterial agent. Active against both Gram-positive and Gram-negative bacteria. Inhibits the initiation stage of bacterial protein synthesis by binding to the inter-subunit bridge B2a on the...
Reference: AG-CN2-0339-M025
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Anthracene antibiotic. Antibacterial agent. Active against both Gram-positive and Gram-negative bacteria. Inhibits the initiation stage of bacterial protein synthesis by binding to the inter-subunit bridge B2a on the...
Reference: AG-CN2-0416-M001
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Antibiotic. Potent and highly selective Ca2+ ionophore. Commonly used to modify intracellular calcium levels to study calcium transport across biological membranes and to calibrate fluorescent Ca2+ indicators....
Reference: AG-CN2-0416-M005
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Antibiotic. Potent and highly selective Ca2+ ionophore. Commonly used to modify intracellular calcium levels to study calcium transport across biological membranes and to calibrate fluorescent Ca2+ indicators....
Reference: AG-CN2-0418-M001
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Antibiotic. Potent and highly selective Ca2+ ionophore. Commonly used to modify intracellular calcium levels to study calcium transport across biological membranes and to calibrate fluorescent Ca2+ indicators....
Reference: AG-CN2-0418-M005
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Antibiotic. Potent and highly selective Ca2+ ionophore. Commonly used to modify intracellular calcium levels to study calcium transport across biological membranes and to calibrate fluorescent Ca2+ indicators....
Reference: AG-CN2-0419-M100
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Antibiotic. Shows antiviral, antifungal and antitumor properties. Immunosuppressive drug used to prevent rejection in organ transplantation, rheumatoid arthritis, and psoriasis. Potent reversible inhibitor of...
Reference: AG-CN2-0419-M500
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Antibiotic. Shows antiviral, antifungal and antitumor properties. Immunosuppressive drug used to prevent rejection in organ transplantation, rheumatoid arthritis, and psoriasis. Potent reversible inhibitor of...
Reference: AG-CN2-0420-M001
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Macrolide antibiotic. Ethyl analog of FK506. Strong immunosuppressant. Binds to the FK-506-binding protein FKBP12. This complex inhibits calcineurin (protein phosphatase 2B (PP2B)). Suppresses the production of T...
Reference: AG-CN2-0420-M005
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Macrolide antibiotic. Ethyl analog of FK506. Strong immunosuppressant. Binds to the FK-506-binding protein FKBP12. This complex inhibits calcineurin (protein phosphatase 2B (PP2B)). Suppresses the production of T...
Reference: AG-CN2-0420-M025
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Macrolide antibiotic. Ethyl analog of FK506. Strong immunosuppressant. Binds to the FK-506-binding protein FKBP12. This complex inhibits calcineurin (protein phosphatase 2B (PP2B)). Suppresses the production of T...
Reference: AG-CN2-0422-C050
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Antibiotic. Potent anticancer compound. Cell permeable, potent, selective and irreversible 20S proteasome inhibitor. Predominantly inhibits the chymotrypsin-like (CTRL) activity of the proteasome. Exhibits lower level...
Reference: AG-CN2-0422-C100
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Antibiotic. Potent anticancer compound. Cell permeable, potent, selective and irreversible 20S proteasome inhibitor. Predominantly inhibits the chymotrypsin-like (CTRL) activity of the proteasome. Exhibits lower level...
Reference: AG-CN2-0422-C250
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Antibiotic. Potent anticancer compound. Cell permeable, potent, selective and irreversible 20S proteasome inhibitor. Predominantly inhibits the chymotrypsin-like (CTRL) activity of the proteasome. Exhibits lower level...
Reference: AG-CN2-0422-C500
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Antibiotic. Potent anticancer compound. Cell permeable, potent, selective and irreversible 20S proteasome inhibitor. Predominantly inhibits the chymotrypsin-like (CTRL) activity of the proteasome. Exhibits lower level...
Reference: AG-CN2-0423-C500
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Antibiotic. Weak cytotoxic towards bacterial and cancer cell lines. 5-Lipoxygenase (5-LOX) inhibitor. Shows DPPH (2,2-diphenyl-1-picrylhydrazyl) radical-scavening activity.
Reference: AG-CN2-0429-C100
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Benzoquinone ansamycin antibiotic. Herbicidal compound. Potent, selective, irreversible and cell permeable protein tyrosine kinase inhibitor. Inhibitor of v-Src, Yes, Fps, Ros, Bcr-Abl and ErbB oncogene products....
Reference: AG-CN2-0429-M001
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Benzoquinone ansamycin antibiotic. Herbicidal compound. Potent, selective, irreversible and cell permeable protein tyrosine kinase inhibitor. Inhibitor of v-Src, Yes, Fps, Ros, Bcr-Abl and ErbB oncogene products....
Reference: AG-CN2-0435-C500
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Anticancer compound. NF-kappaB inhibitor. Apoptosis inducer. Potent anti-inflammatory agent. Telomerase inhibitor. Anti-trypanosomal and antiprotozoal compound Antibiotic. Shows anti-proliferative effects in 3T3-L1...
Reference: AG-CN2-0435-M001
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Anticancer compound. NF-kappaB inhibitor. Apoptosis inducer. Potent anti-inflammatory agent. Telomerase inhibitor. Anti-trypanosomal and antiprotozoal compound Antibiotic. Shows anti-proliferative effects in 3T3-L1...
Reference: AG-CN2-0438-C500
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Antibiotic. Antibacterial against Gram positive and Gram negative bacteria. Exhibits chemotherapeutic activity. Blocks tumor cell invasion and restores cancer cell susceptibility to apoptosis in vitro. Uncouples...
Reference: AG-CN2-0440-C500
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Antibiotic. Inhibits the growth of several Gram-positive and Gram-negative bacteria. Binds to MreB inducing disruption of the bacterial cell wall. Competitive inhibitor of muscarinic acetylcholine receptors (mAChR)....
Reference: AG-CN2-0451-M001
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Mycotoxin. Alkaloid antibiotic. Bacterial enoyl-acyl carrier protein reductase (FabI) inhibitor. Antineoplastic activity. Moderate cytotoxicity against A-549 and HL-60 cell lines. Induces cell cycle arrest through...
Reference: AG-CN2-0453-M001
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Antibiotic. Anti-mycobacterial.
Reference: AG-CN2-0470-C100
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Potent inhibitor of human 5-lipoxygenase (5-LO). This enzyme catalyzes two initial steps in the conversion of arachidonic acid into leukotrienes, well known mediators of inflammatory and allergic reactions....
Reference: AG-CN2-0470-M001
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Potent inhibitor of human 5-lipoxygenase (5-LO). This enzyme catalyzes two initial steps in the conversion of arachidonic acid into leukotrienes, well known mediators of inflammatory and allergic reactions....
Reference: AG-CN2-0471-C500
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Antibiotic. Exhibits broad activity against Gram-positive bacteria. Bacterial cell division protein FtsZ inhibitor (IC50=8.2µg/ml). Inhibits the GTPase activity of FtsZ in vitro (IC50=7.0µg/ml). Induces apoptosis and...
Reference: AG-CN2-0477-MC05
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Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic. Incorporation into the cell membrane forms...
Reference: AG-CN2-0478-M001
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Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic. Incorporation into the cell membrane forms...
Reference: AG-CN2-0479-M001
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Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic (less ionophoric than Enniatin A). Incorporation...
Reference: AG-CN2-0480-M001
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Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic. Incorporation into the cell membrane forms...
Reference: AG-CN2-0491-M001
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Metabolite of aloesin. Potent antioxidant (DPPH assay). Antibiotic. Antifungal. Moderate BACE inhibitor.
Reference: AG-CN2-0494-M001
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Antibiotic. Moderate antibacterial and antifungal agent. Inhibits the autophosphorylation of histidine kinase WalK/YycG. The WalK/WalR (aka YycG/YycF) two-component system is indispensable in the signal transduction...
Reference: AG-CN2-0495-M001
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Antibiotic. Antimicrobial, anti-inflammatory, anticancer and immunosuppressive compound. Shown to have hepatoprotective and hypoglycemic activity. Apoptosis inducer in cancer cells. Sensitizes cancer cells. Induces...
Reference: AG-CN2-0497-M001
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Anthraquinone antibiotic. Moderate antibacterial agent. Photosensitizer (through ROS production) and leaf necrosis inducer. Antiproliferative. Moderate cytotoxic in selected cancer cells. Shown to inhibit several...
Reference: AG-CN2-0498-M001
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Antibiotic. Antibacterial and antifungal compound. Displays antibiotic activity against Gram-negative multidrug resistant bacteria. Anticancer compound. DNA polymerase inhibitor. Enhances TRAIL-induced apoptosis via...
Reference: AG-CN2-0502-M001
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Antioxidant. Reactive oxygen species (ROS) scavenger. Specific ligand of the coactivator CBP/p300, binding to the GACKIX domain. Efficiently inhibits binding of activators at two binding sites. Antibiotic. Potent...
Reference: AG-CN2-0512-M100
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Very potent polymyxin antibiotic. Has only one amino acid difference compared to polymyxin B. Antimicrobial. Targets the lipopolysaccharide (LPS) of the outer membrane of Gram-negative bacteria. Competitively...
Reference: AG-CN2-0512-G001
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Very potent polymyxin antibiotic. Has only one amino acid difference compared to polymyxin B. Antimicrobial. Targets the lipopolysaccharide (LPS) of the outer membrane of Gram-negative bacteria. Competitively...
Reference: AG-CN2-0512-G005
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Very potent polymyxin antibiotic. Has only one amino acid difference compared to polymyxin B. Antimicrobial. Targets the lipopolysaccharide (LPS) of the outer membrane of Gram-negative bacteria. Competitively...
Reference: AG-CN2-0513-M005
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Antibiotic and antifungal compound. Inhibitor of bacterial fatty acid synthesis (inhibits FabH, FabB and FabF condensation enzymes). Irreversible fatty acid synthase (FAS) inhibitor. Inhibits sterol and fatty acid...
Reference: AG-CN2-0513-M025
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Antibiotic and antifungal compound. Inhibitor of bacterial fatty acid synthesis (inhibits FabH, FabB and FabF condensation enzymes). Irreversible fatty acid synthase (FAS) inhibitor. Inhibits sterol and fatty acid...
Reference: AG-CN2-0517-M001
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Potent mitochondrial ATP synthase (ATPases (F1F0)) inhibitor, consequently leading to inhibition of oxidative phosphorylation (OXPHOS). Useful agent for immunometabolism research. Inhibits ATP synthase by blocking its...
Reference: AG-CN2-0517-M005
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Potent mitochondrial ATP synthase (ATPases (F1F0)) inhibitor, consequently leading to inhibition of oxidative phosphorylation (OXPHOS). Useful agent for immunometabolism research. Inhibits ATP synthase by blocking its...
Reference: AG-CN2-0517-M010
€0.00 (tax incl.)
Potent mitochondrial ATP synthase (ATPases (F1F0)) inhibitor, consequently leading to inhibition of oxidative phosphorylation (OXPHOS). Useful agent for immunometabolism research. Inhibits ATP synthase by blocking its...
Reference: AG-CN2-0520-M001
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Orally available Rapamycin derivative that shows improved pharmacokinetics and pharmacodynamics. Potent immunosuppressant. Binds with high affinity to the...
Reference: AG-CN2-0520-M005
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Orally available Rapamycin derivative that shows improved pharmacokinetics and pharmacodynamics. Potent immunosuppressant. Binds with high affinity to the...
Reference: AG-CN2-0520-M025
€0.00 (tax incl.)
Macrolide antibiotic, inhibiting bacterial protein synthesis. Orally available Rapamycin derivative that shows improved pharmacokinetics and pharmacodynamics. Potent immunosuppressant. Binds with high affinity to the...
Reference: AG-CN2-0523-M001
€0.00 (tax incl.)
Antibiotic, antifungal and antiprotozoal agent. Potent and reversible, cell permeable inhibitor of class I and II histone deacetylases (HDACs). Anticancer, immunosuppressive, antifibrogenic compound. Induces apoptosis...
Reference: AG-CN2-0523-M005
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Antibiotic, antifungal and antiprotozoal agent. Potent and reversible, cell permeable inhibitor of class I and II histone deacetylases (HDACs). Anticancer, immunosuppressive, antifibrogenic compound. Induces apoptosis...
Reference: AG-CN2-0527-M001
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Mycotoxin. Biosynthetic precursor of aflatoxins. Antibiotic. Shows moderate antibacterial activity against Gram-positive bacteria. Oxidative phosphorylation (OXPHOS) inhibitor. Inhibits succinate cytochrome c...
Reference: AG-CN2-0529-M001
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Meroterpenoid antibiotic. Anticancer, antimicrobial, antimalarial and amoebicidal compound. Potent, selective and covalent inhibitor of methionine aminopeptidase-2 (MetAP2). Anti-angiogenic by impairing the growth of...
Reference: AG-CN2-0529-M005
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Meroterpenoid antibiotic. Anticancer, antimicrobial, antimalarial and amoebicidal compound. Potent, selective and covalent inhibitor of methionine aminopeptidase-2 (MetAP2). Anti-angiogenic by impairing the growth of...
Reference: AG-CN2-0529-M025
€0.00 (tax incl.)
Meroterpenoid antibiotic. Anticancer, antimicrobial, antimalarial and amoebicidal compound. Potent, selective and covalent inhibitor of methionine aminopeptidase-2 (MetAP2). Anti-angiogenic by impairing the growth of...
Reference: AG-CP3-7000-M005
€0.00 (tax incl.)
Potent, competitive and reversible cysteine, serine and threonine protease inhibitor. Inhibits calpain, kallikrein, trypsin, plasmin, papain and cathepsin B. Does not inhibit pepsin, elastase, renin, cathepsins A and...
Reference: AG-CP3-7000-M025
€0.00 (tax incl.)
Potent, competitive and reversible cysteine, serine and threonine protease inhibitor. Inhibits calpain, kallikrein, trypsin, plasmin, papain and cathepsin B. Does not inhibit pepsin, elastase, renin, cathepsins A and...
Reference: AG-CP3-7000-M100
€0.00 (tax incl.)
Potent, competitive and reversible cysteine, serine and threonine protease inhibitor. Inhibits calpain, kallikrein, trypsin, plasmin, papain and cathepsin B. Does not inhibit pepsin, elastase, renin, cathepsins A and...
Reference: AG-CR1-0162-M001
€0.00 (tax incl.)
Analog of the anticancer drug sorafenib. PK150 is a potent antibiotic. It shows oral bioavailability and antibacterial activity against several pathogenic strains at submicromolar concentrations. PK150 inhibits...

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