Category: Reagents

Reference: BVT-0304-C500
€0.00 (tax incl.)
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-0303-M005
€0.00 (tax incl.)
Oxidoreductase inhibitor. Antitrypanosomal, antibacterial, antifungal, insecticidal and pesticidal. Antitumor compound.
Reference: BVT-0303-M001
€0.00 (tax incl.)
Oxidoreductase inhibitor. Antitrypanosomal, antibacterial, antifungal, insecticidal and pesticidal. Antitumor compound.
Reference: BVT-0297-M005
€0.00 (tax incl.)
Indole alkaloid. Monoamine oxidase inhibitor (MAOI). Antiepileptic (anticonvulsant) compound. Inhibitor of platelet aggregation and thromboxane A2 synthesis. Weak antifungal and antituberculosis activity. Useful as...
Reference: BVT-0297-M001
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Indole alkaloid. Monoamine oxidase inhibitor (MAOI). Antiepileptic (anticonvulsant) compound. Inhibitor of platelet aggregation and thromboxane A2 synthesis. Weak antifungal and antituberculosis activity. Useful as...
Reference: BVT-0292-M001
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Antibiotic. Antibacterial, antifungal and antiviral. Antitumor compound.
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: BVT-0289-M001
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Phytotoxic, antifungal and anthelmintic. Prolyl endopeptidase inhibitor.
Reference: BVT-0289-C500
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Phytotoxic, antifungal and anthelmintic. Prolyl endopeptidase inhibitor.
Reference: BVT-0287-M001
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Weak phosphodiesterase inhibitor.
Reference: BVT-0286-M001
€0.00 (tax incl.)
Analog of agistatin A. Cholesterol biosynthesis inhibitor.
Reference: BVT-0284-M001
€0.00 (tax incl.)
Nucleoside antibiotic. Antitumor compound. Xanthosine monophosphate (XMP) aminase inhibitor. Antimetabolite of the purine biosynthesis.
Reference: BVT-0283-M001
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Hypolipidemic. Cholesterol biosynthesis inhibitor.
Reference: BVT-0280-M001
€0.00 (tax incl.)
Antibiotic. Chromone derivative. Antifungal and antibacterial against Gram-positive and Gram-negative bacteria.
Reference: BVT-0279-M001
€0.00 (tax incl.)
Phytotoxin (Fruit rot toxin). Antibiotic. Antibacterial and antifungal compound.
Reference: BVT-0267-M005
€0.00 (tax incl.)
Antibiotic. Antitumor compound. Powerful, selective inhibitor of nucleic acid synthesis in vitro. Potent hypoxia-inducible factor 1 (HIF-1) DNA binding activity inhibitor. Apoptosis inducer. Antibacterial, antifungal...
Reference: BVT-0267-M001
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Antibiotic. Antitumor compound. Powerful, selective inhibitor of nucleic acid synthesis in vitro. Potent hypoxia-inducible factor 1 (HIF-1) DNA binding activity inhibitor. Apoptosis inducer. Antibacterial, antifungal...
Reference: BVT-0266-M001
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Natural benzodiazepine. Anti-inflammatory.
Reference: BVT-0265-M001
€0.00 (tax incl.)
Ansamycin antibiotic. Antibacterial and antifungal.
Reference: BVT-0264-M001
€0.00 (tax incl.)
Antibiotic. Antibacterial. Active against Gram-positive bacteria. Rasfarnesyltransferase inhibitor. Apoptosis (Caspase-1) inhibitor. AChE inhibitor.
Reference: BVT-0263-M001
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16-membered macrolide antibiotic. Broad spectrum antimicrobial. Antibacterial and antifungal. Protein biosynthesis inhibitor.
Reference: BVT-0263-C500
€0.00 (tax incl.)
16-membered macrolide antibiotic. Broad spectrum antimicrobial. Antibacterial and antifungal. Protein biosynthesis inhibitor.
Reference: BVT-0262-M001
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Pyridone metabolite. Nitric oxide synthase (NOS) inhibitor, showing selectivity for eNOS (NOS III) versus nNOS (NOS I). Thaxtomine biosynthesis inhibitor. Mitochondrial electron transport chain inhibitor.
Reference: BVT-0262-C500
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Pyridone metabolite. Nitric oxide synthase (NOS) inhibitor, showing selectivity for eNOS (NOS III) versus nNOS (NOS I). Thaxtomine biosynthesis inhibitor. Mitochondrial electron transport chain inhibitor.
Reference: BVT-0261-M001
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Antibiotic. Antitumor compound. Shows weak cytotoxicity against different tumor cell lines.
Reference: BVT-0260-M001
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Antibiotic. Nematicidal, insecticidal, antibacterial and antifungal.
Reference: BVT-0258-M001
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Antibiotic. Semisynthetic water-soluble derivative of rebeccamycin (Prod. No. BVT-0139). Antitumor compound. Topoisomerase II (Topo II) inhibitor. DNA intercalating agent.
Reference: BVT-0258-C250
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Antibiotic. Semisynthetic water-soluble derivative of rebeccamycin (Prod. No. BVT-0139). Antitumor compound. Topoisomerase II (Topo II) inhibitor. DNA intercalating agent.
Reference: BVT-0256-M001
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Antibiotic. Antitumor compound. Weakly active against Gram-positive bacteria and fungi. Mediates a unique cross-linking reaction between DNA and histone H3 by light. Single strand scission and covalent binding to DNA...
Reference: BVT-0256-C250
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Antibiotic. Antitumor compound. Weakly active against Gram-positive bacteria and fungi. Mediates a unique cross-linking reaction between DNA and histone H3 by light. Single strand scission and covalent binding to DNA...
Reference: BVT-0256-C100
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Antibiotic. Antitumor compound. Weakly active against Gram-positive bacteria and fungi. Mediates a unique cross-linking reaction between DNA and histone H3 by light. Single strand scission and covalent binding to DNA...
Reference: BVT-0255-M001
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Less toxic, more potent synthetic derivative of geldanamycin (Prod. No. BVT-0196). Angiogenesis inhibitor. Heat shock protein 90 (HSP90) inhibitor. Apoptosis inducer. Shows higher antitumor activity than 17-AAG (Prod....
Reference: BVT-0255-C100
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Less toxic, more potent synthetic derivative of geldanamycin (Prod. No. BVT-0196). Angiogenesis inhibitor. Heat shock protein 90 (HSP90) inhibitor. Apoptosis inducer. Shows higher antitumor activity than 17-AAG (Prod....
Reference: BVT-0254-C500
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Antibiotic. Vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal pH and thus inactivating the lysosomal acid hydrolases. Anti-osteoporotic. Antiviral. Immunosuppressive....
Reference: BVT-0254-C100
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Antibiotic. Vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal pH and thus inactivating the lysosomal acid hydrolases. Anti-osteoporotic. Antiviral. Immunosuppressive....
Reference: BVT-0254-C025
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Antibiotic. Vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal pH and thus inactivating the lysosomal acid hydrolases. Anti-osteoporotic. Antiviral. Immunosuppressive....
Reference: BVT-0253-C500
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Antibiotic. Exhibits similar activity as concanamycin A (Prod. No. BVT-0237) and concanamycin C (Prod. No. BVT-0254). Specific vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal...
Reference: BVT-0253-C100
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Antibiotic. Exhibits similar activity as concanamycin A (Prod. No. BVT-0237) and concanamycin C (Prod. No. BVT-0254). Specific vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal...
Reference: BVT-0253-C025
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Antibiotic. Exhibits similar activity as concanamycin A (Prod. No. BVT-0237) and concanamycin C (Prod. No. BVT-0254). Specific vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal...
Reference: BVT-0252-M001
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Macrolide antibiotic. Specific vacuolar-type H+-ATPase inhibitor. Distinguishes among different types of ATPases. Inhibitor of endosomal, lysosomal and vacuolar acidification. Prevents lysosomal Ca2+ uptake. Inhibitor...
Reference: BVT-0252-C100
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Macrolide antibiotic. Specific vacuolar-type H+-ATPase inhibitor. Distinguishes among different types of ATPases. Inhibitor of endosomal, lysosomal and vacuolar acidification. Prevents lysosomal Ca2+ uptake. Inhibitor...
Reference: BVT-0251-M005
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Antibiotic. HIV-1 reverse transcriptase inhibitor. Human telomerase inhibitor. Cytostatic against different tumor cell lines.
Reference: BVT-0251-M001
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Antibiotic. HIV-1 reverse transcriptase inhibitor. Human telomerase inhibitor. Cytostatic against different tumor cell lines.
Reference: BVT-0250-M001
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Isochromane quinone antibiotic. Antibacterial.
Reference: BVT-0246-M001
€0.00 (tax incl.)
Antibiotic. Antitumor compound. Antifungal. Inhibits osteoclastic bone resorption.
Reference: BVT-0244-M005
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Potent, less toxic analog of geldanamycin (Prod. No. BVT-0196). Inhibits the essential ATPase activity of HSP90. Telomerase activity inhibitor. Apoptosis inducer. Antitumor compound.
Reference: BVT-0244-M001
€0.00 (tax incl.)
Potent, less toxic analog of geldanamycin (Prod. No. BVT-0196). Inhibits the essential ATPase activity of HSP90. Telomerase activity inhibitor. Apoptosis inducer. Antitumor compound.
Reference: BVT-0244-C100
€0.00 (tax incl.)
Potent, less toxic analog of geldanamycin (Prod. No. BVT-0196). Inhibits the essential ATPase activity of HSP90. Telomerase activity inhibitor. Apoptosis inducer. Antitumor compound.
Reference: BVT-0237-M005
€0.00 (tax incl.)
Antibiotic. More potent and specific H+-ATPase inhibitor than bafilomycin A1 (Prod. No. BVT-0252). Inhibits acidification of organelles such as lysosomes and the Golgi apparatus. Inhibitor of autophagic degradation by...
Reference: BVT-0237-M001
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Antibiotic. More potent and specific H+-ATPase inhibitor than bafilomycin A1 (Prod. No. BVT-0252). Inhibits acidification of organelles such as lysosomes and the Golgi apparatus. Inhibitor of autophagic degradation by...
Reference: BVT-0237-C100
€0.00 (tax incl.)
Antibiotic. More potent and specific H+-ATPase inhibitor than bafilomycin A1 (Prod. No. BVT-0252). Inhibits acidification of organelles such as lysosomes and the Golgi apparatus. Inhibitor of autophagic degradation by...
Reference: BVT-0237-C025
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Antibiotic. More potent and specific H+-ATPase inhibitor than bafilomycin A1 (Prod. No. BVT-0252). Inhibits acidification of organelles such as lysosomes and the Golgi apparatus. Inhibitor of autophagic degradation by...
Reference: BVT-0231-M005
€0.00 (tax incl.)
Tricyclic analog of agistatin A . Cholesterol biosynthesis inhibitor. Mycotoxin.
Reference: BVT-0231-M001
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Tricyclic analog of agistatin A . Cholesterol biosynthesis inhibitor. Mycotoxin.
Reference: BVT-0229-M010
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Modified base of mammalian DNA. Involved in regulation of stem cell processes, cellular development, neurodegeneration and carcinogenesis. Important epigenetic marker. Related to bacimethrin (Prod. No. BVT-0226...
Reference: BVT-0228-M001
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Isochromane quinone antibiotic. Antibacterial. Inhibits Trichomonas vaginalis (in vitro and in vivo). Inhibitor of the RNA synthesis.
Reference: BVT-0226-M001
€0.00 (tax incl.)
Derivative of 5-Hydoxymethylcytosine (Prod. No. BVT-0229). Antibiotic. Antibacterial. Thiamine antagonist. Phosphatase kinase inhibitor
Reference: BVT-0226-C500
€0.00 (tax incl.)
Derivative of 5-Hydoxymethylcytosine (Prod. No. BVT-0229). Antibiotic. Antibacterial. Thiamine antagonist. Phosphatase kinase inhibitor
Reference: BVT-0223-M005
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Tricyclic analog of agistatin A. Cholesterol biosynthesis inhibitor.
Reference: BVT-0223-M001
€0.00 (tax incl.)
Tricyclic analog of agistatin A. Cholesterol biosynthesis inhibitor.
Reference: BVT-0212-M001
€0.00 (tax incl.)
Shows weak cytotoxic activity against different tumor cell lines. Has antiparasitic activity.
Reference: BVT-0206-M005
€0.00 (tax incl.)
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: 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-0198-M005
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Antibiotic. Antibacterial. Moderate cytotoxic.
Reference: BVT-0198-M001
€0.00 (tax incl.)
Antibiotic. Antibacterial. Moderate cytotoxic.
Reference: BVT-0196-M005
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Antibiotic. Potent antitumor compound. pp60src tyrosine kinase inhibitor. Inhibits c-mycgene expression in murine lymphoblastoma cells. Inhibits the transforming activity of abl, erbB, fps, src and yes. Binds...
Reference: BVT-0196-M001
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Antibiotic. Potent antitumor compound. pp60src tyrosine kinase inhibitor. Inhibits c-mycgene expression in murine lymphoblastoma cells. Inhibits the transforming activity of abl, erbB, fps, src and yes. Binds...
Reference: BVT-0196-C500
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Antibiotic. Potent antitumor compound. pp60src tyrosine kinase inhibitor. Inhibits c-mycgene expression in murine lymphoblastoma cells. Inhibits the transforming activity of abl, erbB, fps, src and yes. Binds...
Reference: BVT-0196-C100
€0.00 (tax incl.)
Antibiotic. Potent antitumor compound. pp60src tyrosine kinase inhibitor. Inhibits c-mycgene expression in murine lymphoblastoma cells. Inhibits the transforming activity of abl, erbB, fps, src and yes. Binds...
Reference: BVT-0193-M010
€0.00 (tax incl.)
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-0190-M001
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Protein transport from ER to Golgi inhibitor. ADP-ribosylation factor (Arf) inhibitor. Cytotoxic. Antibiotic. Antiviral. Apoptosis inducer. Antitumor compound. Intracellular collagen degradation inhibitor Reviews.
Reference: BVT-0189-M001
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Mycotoxin. Cytotoxic. Tremorgenic. Potent and specific inhibitor of the breast cancer resistance protein (BCRP; ABCG2). Reverses multidrug resistance mediated by BCRP and increases cytotoxicity of several anticancer...
Reference: BVT-0189-C250
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Mycotoxin. Cytotoxic. Tremorgenic. Potent and specific inhibitor of the breast cancer resistance protein (BCRP; ABCG2). Reverses multidrug resistance mediated by BCRP and increases cytotoxicity of several anticancer...
Reference: BVT-0185-M001
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Antibiotic. Active against Gram-positive bacteria, protozoa and tumors. Testosterone 5alpha-reductase inhibitor. Nitric oxide synthase (NOS) inhibitor. Immunosuppressive. Enhances the antifungal activity of rapamycin.
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: BVT-0169-M005
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Mycotoxin. Intermediate of the biosynthetic pathway to aflatoxin B1. Cytotoxic against human solid tumor cell lines.
Reference: BVT-0169-M001
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Mycotoxin. Intermediate of the biosynthetic pathway to aflatoxin B1. Cytotoxic against human solid tumor cell lines.
Reference: BVT-0161-M005
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Antibiotic. Inhibitor of HIF-1 formation by disrupting the binding of p300 to both HIF-1alpha and HIF-2alpha. Histone H3K9 methyltransferases G9a and Suv39h inhibitor. Tumor growth inhibitor. Angiogenesis inhibitor....
Reference: BVT-0161-M001
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Antibiotic. Inhibitor of HIF-1 formation by disrupting the binding of p300 to both HIF-1alpha and HIF-2alpha. Histone H3K9 methyltransferases G9a and Suv39h inhibitor. Tumor growth inhibitor. Angiogenesis inhibitor....
Reference: BVT-0158-M001
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Derivative of the farnesyltransferase inhibitor Manumycin A (Prod. No. BVT-0091 http://www.adipogen.com/bvt-0091/manumycin-a.html ). This compound has not yet been thoroughly tested for its biological activity.
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-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: BVT-0150-M005
€0.00 (tax incl.)
Antibiotic. Antibacterial, antifungal and antiprotozoal. Cytotoxic against several tumor cell lines in vitro.
Reference: BVT-0150-M001
€0.00 (tax incl.)
Antibiotic. Antibacterial, antifungal and antiprotozoal. Cytotoxic against several tumor cell lines in vitro.
Reference: BVT-0139-M001
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Antibiotic. Weak topoisomerase I (Topo I) inhibitor. Structurally similar to staurosporine. Does not show any inhibitory activity against protein kinases. Shows significant antitumor properties in vitro (IC50 = 480 nM...
Reference: BVT-0139-C250
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Antibiotic. Weak topoisomerase I (Topo I) inhibitor. Structurally similar to staurosporine. Does not show any inhibitory activity against protein kinases. Shows significant antitumor properties in vitro (IC50 = 480 nM...
Reference: BVT-0130-M001
€0.00 (tax incl.)
alpha-Glucosidase inhibitor. Inhibitor of glycoprotein processing. Strong glycosyltransferase (GTF) inhibitor. Angiogenesis inhibitor. Reduces the size of myocardial infarcts.
Reference: BVT-0112-M005
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Polyhydroxylated piperidine alkaloid. alpha-Glucosidase I and II inhibitor. Antidiabetic. Antihyperglycaemic activity. Animal feedstuff additive. Antiviral. Shows anti-HIV activity.
Reference: BVT-0112-M001
€0.00 (tax incl.)
Polyhydroxylated piperidine alkaloid. alpha-Glucosidase I and II inhibitor. Antidiabetic. Antihyperglycaemic activity. Animal feedstuff additive. Antiviral. Shows anti-HIV activity.
Reference: BVT-0107-M001
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Antibiotic. Peptide lactone. Antibacterial agent (selective). Potent narrow-spectrum antibiotic against coryneform actinomycetes (MIC value 88 pM). Quorum sensing modulator. Shows hormonal activity. Inducer of...
Reference: BVT-0107-C500
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Antibiotic. Peptide lactone. Antibacterial agent (selective). Potent narrow-spectrum antibiotic against coryneform actinomycetes (MIC value 88 pM). Quorum sensing modulator. Shows hormonal activity. Inducer of...
Reference: BVT-0100-M001
€0.00 (tax incl.)
Antibiotic. Topoisomerase II inhibitor. Mediates a unique cross-linking reaction between DNA and histidine H3. Anti-neoplastic. Photosensitizing compound. Antitumor compound against human cell lines. Less potent than...

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