Category: Reagents

Reference: 23722-500
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A monoterpene with diverse biological activities; scavenges DPPH and ABTS+ free radicals (IC50s = 2.8 and 30 mM, respectively); reduces APPH-induced hemolysis in isolated human erythrocytes; reduces the growth of T....
Reference: 23722-250
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A monoterpene with diverse biological activities; scavenges DPPH and ABTS+ free radicals (IC50s = 2.8 and 30 mM, respectively); reduces APPH-induced hemolysis in isolated human erythrocytes; reduces the growth of T....
Reference: 23722-100
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A monoterpene with diverse biological activities; scavenges DPPH and ABTS+ free radicals (IC50s = 2.8 and 30 mM, respectively); reduces APPH-induced hemolysis in isolated human erythrocytes; reduces the growth of T....
Reference: 21576-50
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A bicyclic monoterpene with diverse biological activities; reduces the growth of a panel of seven Gram-positive bacteria, seven Gram-negative bacteria, and eight yeast strains (MICs = 0.75-1.29, 1.05-1.59, and...
Reference: 21576-10
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A bicyclic monoterpene with diverse biological activities; reduces the growth of a panel of seven Gram-positive bacteria, seven Gram-negative bacteria, and eight yeast strains (MICs = 0.75-1.29, 1.05-1.59, and...
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: 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: BVT-0365-M001
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Genotoxic mycotoxin. Antitumor compound. Potent iNOS (NOSII) inhibitor. Interferes with cellular respiratory processes.
Reference: BVT-0365-C500
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Genotoxic mycotoxin. Antitumor compound. Potent iNOS (NOSII) inhibitor. Interferes with cellular respiratory processes.
Reference: AG-CN2-0023-M025
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Antibiotic. Potent anti-neutrophil agent with cardioprotective effects. mTOR, DNA-PK, phosphatidylinositol 4-kinases, myosin light chain kinase (MLCK) and mitogen-activated protein kinase (MAPK) inhibitor at high...
Reference: AG-CN2-0023-M005
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Antibiotic. Potent anti-neutrophil agent with cardioprotective effects. mTOR, DNA-PK, phosphatidylinositol 4-kinases, myosin light chain kinase (MLCK) and mitogen-activated protein kinase (MAPK) inhibitor at high...
Reference: AG-CN2-0023-M001
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Antibiotic. Potent anti-neutrophil agent with cardioprotective effects. mTOR, DNA-PK, phosphatidylinositol 4-kinases, myosin light chain kinase (MLCK) and mitogen-activated protein kinase (MAPK) inhibitor at high...
Reference: AG-CN2-0157-M005
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Antibiotic. Anti-viral compound. Antifungal (weak). Anti-protozoal (Trypanosoma, Trichomonas).
Reference: AG-CN2-0157-M001
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Antibiotic. Anti-viral compound. Antifungal (weak). Anti-protozoal (Trypanosoma, Trichomonas).
Reference: AG-CN2-0126-M001
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Steroidal antibiotic. Belongs to the Viridin family, including Wortmannin (Prod. No. AG-CN2-0023 http://www.adipogen.com/ag-cn2-0023/wortmannin.html ). Antifungal. Phytotoxin. Shows necrotic activity on plants....
Reference: AG-CN2-0126-C250
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Steroidal antibiotic. Belongs to the Viridin family, including Wortmannin (Prod. No. AG-CN2-0023 http://www.adipogen.com/ag-cn2-0023/wortmannin.html ). Antifungal. Phytotoxin. Shows necrotic activity on plants....
Reference: AG-CN2-0172-M001
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Mycotoxin. Tetracycline antibiotic. Potent antibacterial agent with activity against several strains of Staphylococcus aureus, including Methicillin-resistant S. aureus (MRSA) and quinolone-resistant S. aureus (QRSA)....
Reference: BVT-0359-M001
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Genotoxic mycotoxin. Antibacterial (Gram-positive) and insecticidal. Aromatase inhibitor.
Reference: BVT-0359-C500
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Genotoxic mycotoxin. Antibacterial (Gram-positive) and insecticidal. Aromatase inhibitor.
Reference: BVT-0473-M001
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Antibacterial, antifungal and antiprotozoal agent. Quorum sensing metabolite. Antitumor compound. Protective against UV-C irradiation. Possesses immunomodulatory, analgesic and antipyretic activity. Indole-derived...
Reference: BVT-0443-M005
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Fumitremorgin-type alkaloid. Tremorgenic neurotoxic mycotoxin. Selective blocker of KCa1.1 (high-conductance Ca2+-activated K+; BK; maxi-K) channels. Decreases GABA levels in CNS. Increases spontaneous glutamate and...
Reference: BVT-0443-M001
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Fumitremorgin-type alkaloid. Tremorgenic neurotoxic mycotoxin. Selective blocker of KCa1.1 (high-conductance Ca2+-activated K+; BK; maxi-K) channels. Decreases GABA levels in CNS. Increases spontaneous glutamate and...
Reference: BVT-0454-M001
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20-Membered macrolide glycoside. Antibiotic and antifungal agent. Shows antitrypanosomal and antimalarial activity. Potent inhibitor of mitochondrial and bacterial ATP synthase. Inhibitor of F0F1-ATPase....
Reference: BVT-0422-M001
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Tripyrrolic pigment like prodigiosin. Antimalarial agent. Apoptosis inducer. Anticancer agent with multiple modes of action. Immunosuppressant in non-toxic concentrations. Bone resorption inhibitor. Antiulcer agent.
Reference: BVT-0422-C250
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Tripyrrolic pigment like prodigiosin. Antimalarial agent. Apoptosis inducer. Anticancer agent with multiple modes of action. Immunosuppressant in non-toxic concentrations. Bone resorption inhibitor. Antiulcer agent.
Reference: BVT-0013-M001
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Antibiotic. Antifungal. Topoisomerase II (Topo II) inhibitor. Mg2+- and Zn2+-dependent DNA binding agent. Potent anticancer compound.
Reference: BVT-0013-C250
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Antibiotic. Antifungal. Topoisomerase II (Topo II) inhibitor. Mg2+- and Zn2+-dependent DNA binding agent. Potent anticancer compound.
Reference: BVT-0442-M005
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Antibiotic. Antibacterial and antiprotozoal (trypanocidal). Toxic to human A549 lung cells. Necrosis inducer. Toxic to human bronchial epithelial cells. Stimulating the growth of corn seedling roots. Inhibits IL-6...
Reference: BVT-0442-M001
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Antibiotic. Antibacterial and antiprotozoal (trypanocidal). Toxic to human A549 lung cells. Necrosis inducer. Toxic to human bronchial epithelial cells. Stimulating the growth of corn seedling roots. Inhibits IL-6...
Reference: BVT-0152-M005
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Antibiotic. Isomeric to thiotropocin. Antibacterial. Active against Gram-positive and Gram-negative bacteria. Antifungal and anti-nematodical. Shows antitumor activity. Cytotoxic against selected mammalian neuronal...
Reference: BVT-0152-M001
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Antibiotic. Isomeric to thiotropocin. Antibacterial. Active against Gram-positive and Gram-negative bacteria. Antifungal and anti-nematodical. Shows antitumor activity. Cytotoxic against selected mammalian neuronal...
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-CN2-0523-M001
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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-CN2-0108-M005
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Antibiotic. Antifungal. Antiprotozoal. Potent and reversible, cell permeable inhibitor of histone deacetylase (HDAC). Immunosuppressive. Anticancer compound. Antifibrogenic. Apoptosis inducer. Induces cell growth...
Reference: AG-CN2-0108-M001
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Antibiotic. Antifungal. Antiprotozoal. Potent and reversible, cell permeable inhibitor of histone deacetylase (HDAC). Immunosuppressive. Anticancer compound. Antifibrogenic. Apoptosis inducer. Induces cell growth...
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-CN2-0339-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-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: BVT-0391-M001
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Diketopiperazine antibiotic. Biosynthetic precursor of Thaxtomin A (Prod.No. BVT-0206 http://www.adipogen.com/bvt-0206/thaxtomin-a.html ). Phytotoxin. Plant cell necrosis inducer. Induces common scab disease of potato.
Reference: BVT-0206-M005
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Diketopiperazine antibiotic. Phytotoxin. Herbicide. Natural cellulose synthesis inhibitor. Plant cell necrosis inducer. Induces common scab disease of potato.
Reference: BVT-0206-M001
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Diketopiperazine antibiotic. Phytotoxin. Herbicide. Natural cellulose synthesis inhibitor. Plant cell necrosis inducer. Induces common scab disease of potato.
Reference: AG-CN2-0160-M001
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Antibiotic. Stereoisomer of chrodrimanin B, which is an insecticidal compound.
Reference: AG-CN2-0040-M001
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Antibiotic. Antibacterial (weak). Anticancer compound (weak).
Reference: CDX-T0096-G025
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Tetracycline is a broad-spectrum antibiotic that prevents bacterial growth by inhibiting protein synthesis. It binds to a single site in the 30S ribosomal subunit which prevents attachment of aminoacyl tRNA to the...
Reference: CDX-T0096-G005
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Tetracycline is a broad-spectrum antibiotic that prevents bacterial growth by inhibiting protein synthesis. It binds to a single site in the 30S ribosomal subunit which prevents attachment of aminoacyl tRNA to the...
Reference: BVT-0193-M010
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Antibacterial. Phytotoxin. Melanogenesis inhibitor by reducing tyrosinase production via extracellular signal-regulated protein kinase (ERK) activation. Keratinocyte and epidermis proliferation inhibitor. Mycotoxin....
Reference: BVT-0193-M005
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Antibacterial. Phytotoxin. Melanogenesis inhibitor by reducing tyrosinase production via extracellular signal-regulated protein kinase (ERK) activation. Keratinocyte and epidermis proliferation inhibitor. Mycotoxin....
Reference: BVT-0193-M001
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Antibacterial. Phytotoxin. Melanogenesis inhibitor by reducing tyrosinase production via extracellular signal-regulated protein kinase (ERK) activation. Keratinocyte and epidermis proliferation inhibitor. Mycotoxin....
Reference: BVT-0477-M005
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Mycotoxin. Antibacterial and anticancer agent. A cell-permeable quinone epoxide antibiotic. Covalent inhibitor of the bacterial enzyme UDP-N-acetylglucosamine 1-carboxyvinyltransferase (MurA), which catalyzes the...
Reference: BVT-0477-M001
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Mycotoxin. Antibacterial and anticancer agent. A cell-permeable quinone epoxide antibiotic. Covalent inhibitor of the bacterial enzyme UDP-N-acetylglucosamine 1-carboxyvinyltransferase (MurA), which catalyzes the...
Reference: BVT-0463-M010
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Mycotoxin. Tremorgenic toxin. Exhibits antibacterial, antiviral, insecticidal and antitumor activity. Phytotoxic agent. New type of photosystem II inhibitor. Protein synthesis inhibitor in vitro by suppression of the...
Reference: BVT-0463-M005
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Mycotoxin. Tremorgenic toxin. Exhibits antibacterial, antiviral, insecticidal and antitumor activity. Phytotoxic agent. New type of photosystem II inhibitor. Protein synthesis inhibitor in vitro by suppression of the...
Reference: BVT-0463-M001
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Mycotoxin. Tremorgenic toxin. Exhibits antibacterial, antiviral, insecticidal and antitumor activity. Phytotoxic agent. New type of photosystem II inhibitor. Protein synthesis inhibitor in vitro by suppression of the...
Reference: BVT-0456-M010
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Ketolide type macrolide antibiotic. Antibacterial compound used to treat mild to moderate respiratory infections. Protein synthesis inhibitor, by binding to the 50S ribosomal subunit and subsequently blocking the...
Reference: BVT-0456-M001
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Ketolide type macrolide antibiotic. Antibacterial compound used to treat mild to moderate respiratory infections. Protein synthesis inhibitor, by binding to the 50S ribosomal subunit and subsequently blocking the...
Reference: CDX-S0056-M025
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Metabolite of sulfamethoxazole, a sulfonamide bacteriostatic antibiotic. Has been shown to be an important component in sulfonamide hypersensitivity reactions and has been implicated in sulfonamide-mediated...
Reference: CDX-S0056-M010
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Metabolite of sulfamethoxazole, a sulfonamide bacteriostatic antibiotic. Has been shown to be an important component in sulfonamide hypersensitivity reactions and has been implicated in sulfonamide-mediated...
Reference: BVT-0312-M001
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Antifungal. Respiration inhibitor. Blocks the electron transfer between cytochrome b and cytochrome c1.
Reference: BVT-0312-C500
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Antifungal. Respiration inhibitor. Blocks the electron transfer between cytochrome b and cytochrome c1.
Reference: AG-CN2-0046-G001
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Antibiotic. Diabetogenic. Diabetes inducer. Induces diabetes mellitus in animal models through its toxic effects on pancreatic beta-cells. Mutagenic. Potent alkylating agent. Potent DNA methylating agent. Nitric oxide...
Reference: AG-CN2-0046-M250
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Antibiotic. Diabetogenic. Diabetes inducer. Induces diabetes mellitus in animal models through its toxic effects on pancreatic beta-cells. Mutagenic. Potent alkylating agent. Potent DNA methylating agent. Nitric oxide...
Reference: AG-CN2-0046-M050
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Antibiotic. Diabetogenic. Diabetes inducer. Induces diabetes mellitus in animal models through its toxic effects on pancreatic beta-cells. Mutagenic. Potent alkylating agent. Potent DNA methylating agent. Nitric oxide...
Reference: AG-CN2-0141-M001
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Antibiotic. TNF-alpha-induced NF-kappaB activation inhibitor. Antiangiogenic. Apoptosis inducer. Anticancer compound. Selective cytotoxic against several cancer cell lines. Tyrosinase inhibitor.
Reference: AG-CN2-0141-C250
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Antibiotic. TNF-alpha-induced NF-kappaB activation inhibitor. Antiangiogenic. Apoptosis inducer. Anticancer compound. Selective cytotoxic against several cancer cell lines. Tyrosinase inhibitor.
Reference: CDX-S0267-G025
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Stigmasterol is a phytosterol with chemical structure similar to cholesterol and anti-hypercholestrolemic activity. It exhibits anticancer, anti-inflammatory, antioxidant, antidiabetic, neuroprotective and...
Reference: CDX-S0267-G010
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Stigmasterol is a phytosterol with chemical structure similar to cholesterol and anti-hypercholestrolemic activity. It exhibits anticancer, anti-inflammatory, antioxidant, antidiabetic, neuroprotective and...
Reference: CDX-S0267-G005
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Stigmasterol is a phytosterol with chemical structure similar to cholesterol and anti-hypercholestrolemic activity. It exhibits anticancer, anti-inflammatory, antioxidant, antidiabetic, neuroprotective and...
Reference: BVT-0171-M005
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Intermediate of the biosynthetic pathway to aflatoxin B1. Mycotoxin. DNA synthesis inhibitor. Anticancer compound. Cytotoxic, carcinogenic and mutagenic. Acyl-CoA:cholesterol acyltransferase 2 (ACAT2) inhibitor. Shown...
Reference: BVT-0171-M001
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Intermediate of the biosynthetic pathway to aflatoxin B1. Mycotoxin. DNA synthesis inhibitor. Anticancer compound. Cytotoxic, carcinogenic and mutagenic. Acyl-CoA:cholesterol acyltransferase 2 (ACAT2) inhibitor. Shown...
Reference: AG-CN2-0022-M005
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Antibiotic. Antifungal and anti-yeast activity. Inhibits platelet aggregation induced by collagen or ADP. Has no effect on thrombin-induced platelet aggregation. Potent, cell permeable, reversible, ATP-competitive and...
Reference: AG-CN2-0022-M001
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Antibiotic. Antifungal and anti-yeast activity. Inhibits platelet aggregation induced by collagen or ADP. Has no effect on thrombin-induced platelet aggregation. Potent, cell permeable, reversible, ATP-competitive and...
Reference: AG-CN2-0022-C500
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Antibiotic. Antifungal and anti-yeast activity. Inhibits platelet aggregation induced by collagen or ADP. Has no effect on thrombin-induced platelet aggregation. Potent, cell permeable, reversible, ATP-competitive and...
Reference: AG-CN2-0022-C100
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Antibiotic. Antifungal and anti-yeast activity. Inhibits platelet aggregation induced by collagen or ADP. Has no effect on thrombin-induced platelet aggregation. Potent, cell permeable, reversible, ATP-competitive and...
Reference: BVT-0445-M005
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Mycotoxin. Antibiotic (incl. MRSA). Non-peptidic anti-diabetic agent (receptor-selective glucagon antagonist). Inhibitor of botulinum neurotoxin serotype A (BoNTA). Cytotoxic. Antioxidant (free radical scavenger).
Reference: AG-CN2-0001-M001
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Non-peptidic anti-diabetic agent. Receptor-selective glucagon antagonist. Free radical species (·OH, R·) and singlet oxygen (1O2) scavenger. Mycotoxin. Cytotoxic. Antioxidant. Inhibitor of botulinum neurotoxin...
Reference: BVT-0290-M001
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Antibiotic. Bacterial DNA gyrase inhibitor: Staphylococcus aureus (IC50= 1.45µM), E. coli (IC50= 0.41µM). Human topoisomerase II (Topo II) inhibitor (IC50= 100µM). Antibacterial (Gram-positive). Antitumor compound.
Reference: AG-CN2-0146-M001
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Antibiotic. Lariat peptide antiviral. Anti-HIV and anti-HSV (Herpes simplex virus) agent. Fsr quorum sensing inhibitor. Calmodulin-activated myosin light chain kinase (MLCK) inhibitor.
Reference: AG-CN2-0146-C250
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Antibiotic. Lariat peptide antiviral. Anti-HIV and anti-HSV (Herpes simplex virus) agent. Fsr quorum sensing inhibitor. Calmodulin-activated myosin light chain kinase (MLCK) inhibitor.
Reference: BVT-0399-M001
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9,9`-Bianthryl polyketide derivative. Antibiotic. Active against Gram-positive bacteria including mycobacteria. Bacterial cell wall synthesis inhibitor. Antitumor compound.
Reference: BVT-0478-M010
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Seriniquinone is a potent cytotoxic and melanoma-selective anticancer agent. Upon cellular treatment and based on the compounds fluorescent nature it was found localized in the endoplasmic reticulum. Seriniquinone...
Reference: BVT-0478-M005
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Seriniquinone is a potent cytotoxic and melanoma-selective anticancer agent. Upon cellular treatment and based on the compounds fluorescent nature it was found localized in the endoplasmic reticulum. Seriniquinone...
Reference: BVT-0478-M001
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Seriniquinone is a potent cytotoxic and melanoma-selective anticancer agent. Upon cellular treatment and based on the compounds fluorescent nature it was found localized in the endoplasmic reticulum. Seriniquinone...
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-CN2-0054-M005
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Antibiotic. Antibacterial. Weak antagonist of human endothelin receptor A (ETA) and B (ETB). Cholesteryl ester transfer protein (CETP) activity inhibitor. Grb2-Shc binding inhibitor. Potent aldose reductase inhibitor....
Reference: AG-CN2-0054-M001
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Antibiotic. Antibacterial. Weak antagonist of human endothelin receptor A (ETA) and B (ETB). Cholesteryl ester transfer protein (CETP) activity inhibitor. Grb2-Shc binding inhibitor. Potent aldose reductase inhibitor....
Reference: AG-CN2-0054-MC05
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Antibiotic. Antibacterial. Weak antagonist of human endothelin receptor A (ETA) and B (ETB). Cholesteryl ester transfer protein (CETP) activity inhibitor. Grb2-Shc binding inhibitor. Potent aldose reductase inhibitor....
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: BVT-0305-M010
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Acetylcholine esterase and ATPase inhibitor. Ichthyotoxin. Tumorigenesis and JB6 cell transformation inhibitor.
Reference: BVT-0305-M002
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Acetylcholine esterase and ATPase inhibitor. Ichthyotoxin. Tumorigenesis and JB6 cell transformation inhibitor.
Reference: BVT-0382-M001
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Angucycline antibiotic. Antibacterial. Antitumor compound. Active against Gram-positive bacteria and P388 leukaemia cells. Farnesyl-protein transferase inhibitor. Inhibitor of nitric oxide synthase (NOS) (shown for...
Reference: BVT-0382-C500
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Angucycline antibiotic. Antibacterial. Antitumor compound. Active against Gram-positive bacteria and P388 leukaemia cells. Farnesyl-protein transferase inhibitor. Inhibitor of nitric oxide synthase (NOS) (shown for...
Reference: BVT-0444-M005
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Mycotoxin. Antibiotic (Streptococcus, Corynebacterium, MRSA). Antiviral, HIV-1 integrase inhibitor. DNA replication, transcription and repair inhibitor (carcinogenic activity). RNA polymerase and ribonuclease H...
Reference: AG-CN2-0124-M001
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Antibiotic. Antibacteriophage. Antiviral. Mycotoxin. DNA replication, transcription and repair inhibitor. Antibacterial. RNA polymerase and ribonuclease H inhibitor. Insecticidal. Cytotoxic. HIV-1 integrase inhibitor....
Reference: AG-CN2-0124-C250
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Antibiotic. Antibacteriophage. Antiviral. Mycotoxin. DNA replication, transcription and repair inhibitor. Antibacterial. RNA polymerase and ribonuclease H inhibitor. Insecticidal. Cytotoxic. HIV-1 integrase inhibitor....
Reference: BVT-0395-M005
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Monomer of aurofusarin. Mycotoxin. Anticancer and antimycobacterial compound in vivo. Moderate tyrosinase inhibitor. Anti-estrogenic.
Reference: BVT-0395-M001
€0.00 (tax incl.)
Monomer of aurofusarin. Mycotoxin. Anticancer and antimycobacterial compound in vivo. Moderate tyrosinase inhibitor. Anti-estrogenic.

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