Category: Reagents

Reference: BVT-0439-M001
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Eremophilane sesquiterpenoid. Inhibitor of HIV-1 Tat transduction. Phytotoxin. Mycotoxin.
Reference: BVT-0441-M001
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Antibiotic. Antibacterial, cytotoxic, herbicidal and antimalarial compound. Human lipoxygenase inhibitor. Potent myosin ATPase inhibitor. Inhibitor of the non-mevalonate pathway enzyme IspD.
Reference: BVT-0441-C500
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Antibiotic. Antibacterial, cytotoxic, herbicidal and antimalarial compound. Human lipoxygenase inhibitor. Potent myosin ATPase inhibitor. Inhibitor of the non-mevalonate pathway enzyme IspD.
Reference: AG-CN2-0315-M001
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Potent antibacterial agent. Shows MIC values lower than 0.015µg/ml against Gram-positive pathogens, including some antibiotic-resistant strains and selected Gram-negative bacteria.
Reference: AG-CN2-0315-C500
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Potent antibacterial agent. Shows MIC values lower than 0.015µg/ml against Gram-positive pathogens, including some antibiotic-resistant strains and selected Gram-negative bacteria.
Reference: BVT-0308-M001
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Antibiotic. Exists in an equilibrium of diastereomers.
Reference: BVT-0308-C500
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Antibiotic. Exists in an equilibrium of diastereomers.
Reference: BVT-0066-M001
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Spirobisnaphthalene derivative (unpublished). Oxidation product of palmarumycin C3. This compound has not yet been thoroughly tested for its biological activity.
Reference: BVT-0078-M005
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Rasfarnesyltransferase inhibitor. Antifungal, antibacterial and herbicidal. Structurally unique natural products. The basic structure of palmarumycin C1 can be modified by a number of hydroxylation, oxygenation,...
Reference: BVT-0078-M001
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Rasfarnesyltransferase inhibitor. Antifungal, antibacterial and herbicidal. Structurally unique natural products. The basic structure of palmarumycin C1 can be modified by a number of hydroxylation, oxygenation,...
Reference: 23159-100
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A monoterpene with diverse biological activities; inhibits the growth of S. typhimurium, E. coli, L. monocytogenes, S. epidermidis, and S. aureus (MICs = 0.266-0.608% v/v); decreases the invasive activity of HT-1080...
Reference: BVT-0031-M001
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Nucleoside antibiotic (amicetin group). Anticoccidial agent. Shows broad antibacterial activity.
Reference: AG-CN2-0314-C500
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Cinnamoyl aminoglycoside antibiotic. Protein synthesis inhibitor in vitro. Selective inhibitor of bacterial translation elongation, through binding to the 50S subunit. Inhibits EF-G-dependent mRNA translocation but...
Reference: AG-CN2-0158-M005
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Antibiotic. Antimycoplasma. Antifungal compound. Anti-malarial agent. Ras-competitive non-CAAX mimetic type farnesyltransferase (FTase) inhibitor. Potential anticancer compound. Inducer of antiproliferative effects in...
Reference: AG-CN2-0158-M001
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Antibiotic. Antimycoplasma. Antifungal compound. Anti-malarial agent. Ras-competitive non-CAAX mimetic type farnesyltransferase (FTase) inhibitor. Potential anticancer compound. Inducer of antiproliferative effects in...
Reference: AG-CN2-0517-M010
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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-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: BVT-0287-M001
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Weak phosphodiesterase inhibitor.
Reference: AG-CN2-0150-M005
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Antibiotic. Anti-mycobacterial. Siderophore (iron (Fe) chelating compound). Inducer of morphological changes in insect cells. Antioxidant. Anticancer compound.
Reference: AG-CN2-0150-M001
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Antibiotic. Anti-mycobacterial. Siderophore (iron (Fe) chelating compound). Inducer of morphological changes in insect cells. Antioxidant. Anticancer compound.
Reference: AG-CN2-0020-M025
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Antibiotic. High affinity ionophore for monovalent cations such as H+, K+, Na+, Pb2+. Shows antibacterial (Gram-positive), antifungal, antitumor and antiviral activity. Disrupts membrane potential of mitochondria....
Reference: AG-CN2-0020-M005
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Antibiotic. High affinity ionophore for monovalent cations such as H+, K+, Na+, Pb2+. Shows antibacterial (Gram-positive), antifungal, antitumor and antiviral activity. Disrupts membrane potential of mitochondria....
Reference: AG-CN2-0155-M005
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Antibiotic. Antifungal. Nerve growth factor (NGF) potentiator.
Reference: AG-CN2-0155-M001
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Antibiotic. Antifungal. Nerve growth factor (NGF) potentiator.
Reference: AG-CN2-0178-M005
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Antibiotic. Mycotoxin. Very weak cytotoxic activity. Antifungal. Inhibits cell wall biosynthesis. Nerve growth factor (NGF) potentiator.
Reference: AG-CN2-0178-M001
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Antibiotic. Mycotoxin. Very weak cytotoxic activity. Antifungal. Inhibits cell wall biosynthesis. Nerve growth factor (NGF) potentiator.
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: BVT-0304-M001
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Nucleoside analog. Cytotoxic. DNA, RNA and protein synthesis inhibitor. Shows anticancer activity. Anti-mycobacterial. Has tuberculostatic activity. Antifungal activity. Antiviral (anti-Herpes). Adenosine deaminase...
Reference: BVT-0304-C500
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Nucleoside analog. Cytotoxic. DNA, RNA and protein synthesis inhibitor. Shows anticancer activity. Anti-mycobacterial. Has tuberculostatic activity. Antifungal activity. Antiviral (anti-Herpes). Adenosine deaminase...
Reference: BVT-0204-M005
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Antibiotic against Gram-positive bacteria, particularly Staphylococcus and Clostridia. More effective against multi-resistant strains (MRSA) than erythromycin and vancomycin. Inhibits cell proliferation and induces...
Reference: BVT-0204-M001
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Antibiotic against Gram-positive bacteria, particularly Staphylococcus and Clostridia. More effective against multi-resistant strains (MRSA) than erythromycin and vancomycin. Inhibits cell proliferation and induces...
Reference: BVT-0265-M001
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Ansamycin antibiotic. Antibacterial and antifungal.
Reference: AG-CN2-0312-M005
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Antibacterial class I lantibiotic. Inhibits cell wall synthesis and consequently bacterial growth by forming a complex with lipid intermediate II (Lipid II), a key intermediate in peptidoglycan biosynthesis. Interfers...
Reference: AG-CN2-0312-M001
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Antibacterial class I lantibiotic. Inhibits cell wall synthesis and consequently bacterial growth by forming a complex with lipid intermediate II (Lipid II), a key intermediate in peptidoglycan biosynthesis. Interfers...
Reference: AG-CN2-0311-M005
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Antibacterial class I lantibiotic. Inhibits cell wall synthesis and consequently bacterial growth by forming a complex with lipid intermediate II (Lipid II), a key intermediate in peptidoglycan biosynthesis. Interfers...
Reference: AG-CN2-0311-M001
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Antibacterial class I lantibiotic. Inhibits cell wall synthesis and consequently bacterial growth by forming a complex with lipid intermediate II (Lipid II), a key intermediate in peptidoglycan biosynthesis. Interfers...
Reference: AG-CN2-0310-M005
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Actagardin-related class II lantibiotic. Antibacterial with improved activity than actagardine against Staphylococcus spp. and Streptococcus spp. Shows significant activity against Gram-positive anaerobic bacteria,...
Reference: AG-CN2-0310-M001
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Actagardin-related class II lantibiotic. Antibacterial with improved activity than actagardine against Staphylococcus spp. and Streptococcus spp. Shows significant activity against Gram-positive anaerobic bacteria,...
Reference: AG-CN2-0308-C500
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Antibacterial class I lantibiotic. Brominated variant of NAI-107. Inhibits cell wall synthesis and consequently bacterial growth by forming a complex with lipid intermediate II (Lipid II), a key intermediate in...
Reference: AG-CN2-0307-M005
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Antibacterial class I lantibiotic. Mixture of two similarly active and structurally related polypeptides (A1, 2246Da and A2, 2230Da) of 24 amino acids linked by 5 intramolecular thioether bridges. Inhibits cell wall...
Reference: AG-CN2-0307-M001
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Antibacterial class I lantibiotic. Mixture of two similarly active and structurally related polypeptides (A1, 2246Da and A2, 2230Da) of 24 amino acids linked by 5 intramolecular thioether bridges. Inhibits cell wall...
Reference: CDX-A0291-M050
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This is a metabolite of the sulfonamide bacteriostatic antibiotic sulfamethoxazole. Sulfamethoxazole is metabolized via acetylation, catalyzed by liver extramitochondrial N-acetyl transferases. Acetyl-Sulfamethoxazole...
Reference: CDX-A0291-M010
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This is a metabolite of the sulfonamide bacteriostatic antibiotic sulfamethoxazole. Sulfamethoxazole is metabolized via acetylation, catalyzed by liver extramitochondrial N-acetyl transferases. Acetyl-Sulfamethoxazole...
Reference: CDX-A0298-M100
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Metabolite of the long-acting sulfonamide antibiotic sulfadimethoxine, used in freshwater aquaculture. Sulfonamide that is benzenesulfonamide substituted by an acetylamino group at position 4 and a...
Reference: CDX-A0298-M025
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Metabolite of the long-acting sulfonamide antibiotic sulfadimethoxine, used in freshwater aquaculture. Sulfonamide that is benzenesulfonamide substituted by an acetylamino group at position 4 and a...
Reference: BVT-0130-M001
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alpha-Glucosidase inhibitor. Inhibitor of glycoprotein processing. Strong glycosyltransferase (GTF) inhibitor. Angiogenesis inhibitor. Reduces the size of myocardial infarcts.
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-CN2-0470-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: BVT-L002-1
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The Mycotoxin TargoSet™ offers a panel of well-characterized and highly pure compounds for screening experiments, cell-based research or as standard compounds. Mycotoxins are secondary metabolites produced by...
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-CN2-0419-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: BVT-0070-M001
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Antibiotic. Antibacterial. Phytotoxic.
Reference: CDX-M0189-M050
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Moxifloxacin is a fourth-generation synthetic broad-spectrum fluoroquinolone antibiotic. It is used against both Gram-positive and Gram-negative bacteria and to treat bacterial infections associated with bronchitis,...
Reference: CDX-M0161-M025
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Mitomycin C (MMC) is an antitumor antibiotic. This product is an alkylating agent that specifically targets the guanine nucleoside sequence 5‘-CpG-3‘. It inhibits DNA synthesis by covalently reacting with DNA, forming...
Reference: CDX-M0161-M010
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Mitomycin C (MMC) is an antitumor antibiotic. This product is an alkylating agent that specifically targets the guanine nucleoside sequence 5‘-CpG-3‘. It inhibits DNA synthesis by covalently reacting with DNA, forming...
Reference: CDX-M0161-M005
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Mitomycin C (MMC) is an antitumor antibiotic. This product is an alkylating agent that specifically targets the guanine nucleoside sequence 5‘-CpG-3‘. It inhibits DNA synthesis by covalently reacting with DNA, forming...
Reference: BVT-0028-M005
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Antibiotic. Antitumor compound. Cytotoxic.
Reference: BVT-0028-M001
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Antibiotic. Antitumor compound. Cytotoxic.
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-CN2-0159-M005
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Antibiotic. Active against Gram-positive bacteria. Active against Spodoptera eridania.
Reference: AG-CN2-0159-M001
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Antibiotic. Active against Gram-positive bacteria. Active against Spodoptera eridania.
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: BVT-0264-M001
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Antibiotic. Antibacterial. Active against Gram-positive bacteria. Rasfarnesyltransferase inhibitor. Apoptosis (Caspase-1) inhibitor. AChE inhibitor.
Reference: BVT-0091-M010
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Antibiotic. Apoptosis and endoplasmic reticulum stress-mediated cell death inducer. Potent, selective and competitive cell permeable rasfarnesyltransferase inhibitor (IC50 = 30 nM). Does not affect...
Reference: BVT-0091-M005
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Antibiotic. Apoptosis and endoplasmic reticulum stress-mediated cell death inducer. Potent, selective and competitive cell permeable rasfarnesyltransferase inhibitor (IC50 = 30 nM). Does not affect...
Reference: BVT-0091-M001
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Antibiotic. Apoptosis and endoplasmic reticulum stress-mediated cell death inducer. Potent, selective and competitive cell permeable rasfarnesyltransferase inhibitor (IC50 = 30 nM). Does not affect...
Reference: AG-CN2-0107-M001
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Peptide antibiotic. Induces root curvature and malformation in plants. Antibacterial, antimalarial and antitrypanosomal. Disrupts the cell cycle at the G2 checkpoint of cancer cells, leading to sensitization of the...
Reference: AG-CN2-0107-C250
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Peptide antibiotic. Induces root curvature and malformation in plants. Antibacterial, antimalarial and antitrypanosomal. Disrupts the cell cycle at the G2 checkpoint of cancer cells, leading to sensitization of the...
Reference: AG-CN2-0169-M001
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Peptide antibiotic. Antibcaterial. Plant growth stimulator. Induces root curvature and malformation in plants. Mycotoxin. Prevents interleukin-1 (IL-1) induced endothelial changes by inhibition of protein synthesis....
Reference: AG-CN2-0169-C250
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Peptide antibiotic. Antibcaterial. Plant growth stimulator. Induces root curvature and malformation in plants. Mycotoxin. Prevents interleukin-1 (IL-1) induced endothelial changes by inhibition of protein synthesis....
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-CN2-0152-M005
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Antibiotic. Cell-cell adhesion inhibitor. Antimetastatic compound. Antifungal. Antimicrobial.
Reference: AG-CN2-0152-M001
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Antibiotic. Cell-cell adhesion inhibitor. Antimetastatic compound. Antifungal. Antimicrobial.
Reference: AG-CR1-0163-M025
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MAC-545496 is a potent antimicrobial agent against MRSA. It works as a synthetic antibiotic adjuvant, a antivirulence and antibiofilm agent. Potent nanomolar inhibitor of glycopeptide-resistance-associated protein R...
Reference: AG-CR1-0163-M005
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MAC-545496 is a potent antimicrobial agent against MRSA. It works as a synthetic antibiotic adjuvant, a antivirulence and antibiofilm agent. Potent nanomolar inhibitor of glycopeptide-resistance-associated protein R...
Reference: AG-CR1-0163-M001
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MAC-545496 is a potent antimicrobial agent against MRSA. It works as a synthetic antibiotic adjuvant, a antivirulence and antibiofilm agent. Potent nanomolar inhibitor of glycopeptide-resistance-associated protein R...
Reference: BVT-0037-M005
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Antibiotic. Glycopeptide synthesis inhibitor. Antibacterial, antifungal and anticoccidial. Cytotoxic.
Reference: BVT-0037-M001
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Antibiotic. Glycopeptide synthesis inhibitor. Antibacterial, antifungal and anticoccidial. Cytotoxic.
Reference: BVT-0037-C500
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Antibiotic. Glycopeptide synthesis inhibitor. Antibacterial, antifungal and anticoccidial. Cytotoxic.
Reference: BVT-0457-M001
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Nitrophenyl pyranone derivative related to aureothin (Prod. No. BVT-0303 http://www.adipogen.com/bvt-0303/aureothin.html ). Insecticidal and nematocidal compound. Metabolites within this product class show pronounced...
Reference: BVT-0457-C500
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Nitrophenyl pyranone derivative related to aureothin (Prod. No. BVT-0303 http://www.adipogen.com/bvt-0303/aureothin.html ). Insecticidal and nematocidal compound. Metabolites within this product class show pronounced...
Reference: BVT-0467-M005
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Unique fungal allene derivative. Similar to A 82775C and iso-A 82775C. Biological activity not tested yet.
Reference: BVT-0467-M001
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Unique fungal allene derivative. Similar to A 82775C and iso-A 82775C. Biological activity not tested yet.
Reference: BVT-0466-M005
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Unique fungal allene derivative. Similar to A 82775C and iso-A 82775C. Biological activity not tested yet.
Reference: BVT-0466-M001
€0.00 (tax incl.)
Unique fungal allene derivative. Similar to A 82775C and iso-A 82775C. Biological activity not tested yet.
Reference: BVT-0212-M001
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Shows weak cytotoxic activity against different tumor cell lines. Has antiparasitic activity.
Reference: CDX-L0031-M025
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Linezolid is a synthetic oxazolidinone antibiotic with activity against a wide range of Gram-positive bacteria. Displays potent antibacterial activity against a variety of multidrug-resistant gram-positive microbes in...
Reference: AG-CP3-7000-M100
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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
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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-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: BVT-0019-M010
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Mycotoxin. Chelation agent with polyfunctional skeleton for development of biologically active compounds. Moderate antibacterial agent. Tyrosinase inhibitor. Inhibits catecholase activity of tyrosinase....
Reference: BVT-0157-M005
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Antibiotic. Member of the elfermycin group. Antibacterial. Protein biosynthesis inhibitor. Specifically interacts with the bacterial elongation factor EF-Tu and prevents the release of EF-Tu from the bacterial...
Reference: BVT-0157-M001
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Antibiotic. Member of the elfermycin group. Antibacterial. Protein biosynthesis inhibitor. Specifically interacts with the bacterial elongation factor EF-Tu and prevents the release of EF-Tu from the bacterial...
Reference: BVT-0001-C500
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Antibiotic. Potent endothelin receptor antagonist. Anti-osteoporotic. Antibacterial. Cytotoxic. Mediates its cytotoxic effects, at least in part, through proteasome inhibition.
Reference: BVT-0001-C100
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Antibiotic. Potent endothelin receptor antagonist. Anti-osteoporotic. Antibacterial. Cytotoxic. Mediates its cytotoxic effects, at least in part, through proteasome inhibition.
Reference: AG-CN2-0097-M005
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Indolocarbazole alkaloid antibiotic.. Potent cell permeable reversible and ATP-competitive PKC (protein kinase C) inhibitor with 10-fold selectivity over PKA (protein kinase A). Anticancer compound. Cytotoxic againt...

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