Category: Reagents

Reference: BVT-0254-M001
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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-M001
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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: 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: 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: 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: 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: CDX-M0091-G001
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A main acid metabolite of the antibiotic metronidazole showing some antibacterial activity. Compound can be used as analytical reference material.
Reference: CDX-M0091-M100
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A main acid metabolite of the antibiotic metronidazole showing some antibacterial activity. Compound can be used as analytical reference material.

IDA

Reference: CDX-M0001-M250
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Amino compounds having primary groups such as amino acids or aminocyclitol antibiotics lack chromopores or fluorophores in their molecules. Derivatization is required for their detection with high sensitivity using...

IDA

Reference: CDX-M0001-M025
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Amino compounds having primary groups such as amino acids or aminocyclitol antibiotics lack chromopores or fluorophores in their molecules. Derivatization is required for their detection with high sensitivity using...

IDA

Reference: CDX-M0001-M005
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Amino compounds having primary groups such as amino acids or aminocyclitol antibiotics lack chromopores or fluorophores in their molecules. Derivatization is required for their detection with high sensitivity using...
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: CDX-J0010-L005
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Josamycin is a member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. It is an antimicrobial against a wide variety of pathogens. It has activity against Gram-positive an...
Reference: CDX-J0010-L001
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Josamycin is a member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. It is an antimicrobial against a wide variety of pathogens. It has activity against Gram-positive an...
Reference: CDX-J0009-L005
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Josamycin is a member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. It is an antimicrobial against a wide variety of pathogens. It has activity against Gram-positive an...
Reference: CDX-J0009-L001
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Josamycin is a member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. It is an antimicrobial against a wide variety of pathogens. It has activity against Gram-positive an...
Reference: CDX-J0001-GG25
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A member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. May overcome anticancer drug resistance by inhibiting the binding of vinblastine or cyclosporin A to P-glycoprotein...
Reference: CDX-J0001-M200
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A member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. May overcome anticancer drug resistance by inhibiting the binding of vinblastine or cyclosporin A to P-glycoprotein...
Reference: CDX-J0001-M050
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A member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. May overcome anticancer drug resistance by inhibiting the binding of vinblastine or cyclosporin A to P-glycoprotein...
Reference: CDX-H0100-M010
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Hydroxystilbamidine (also called Fluoro Gold) is a cationic dye used for staining DNA and RNA. It exhibits distinctively different fluorescence emission profiles when bound to DNA compared to RNA. It is also...
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: CDX-F0079-G025
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Flumequine is a fluoroquinolone synthetic chemotherapeutic antibiotic used to treat bacterial infections. Targets primarily gram negative bacteria, especially those which cause enteric infections in animals. It is...
Reference: CDX-F0079-G005
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Flumequine is a fluoroquinolone synthetic chemotherapeutic antibiotic used to treat bacterial infections. Targets primarily gram negative bacteria, especially those which cause enteric infections in animals. It is...
Reference: CDX-E0574-M001
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Potent immunosuppressant. Binds with high affinity to the FK506 binding protein-12 (FKBP-12) to generate an immunosuppressive complex that inhibits the...
Reference: CDX-E0237-G100
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Ethionamide is an antimycobacterial antibiotic that is active against M. tuberculosis (MICs = 0.3-1.25 µg/ml). Ethionamide is a prodrug activated via oxidation by ethA (a flavin monooxygenase) and leading to the...
Reference: CDX-E0237-G025
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Ethionamide is an antimycobacterial antibiotic that is active against M. tuberculosis (MICs = 0.3-1.25 µg/ml). Ethionamide is a prodrug activated via oxidation by ethA (a flavin monooxygenase) and leading to the...
Reference: CDX-E0237-G005
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Ethionamide is an antimycobacterial antibiotic that is active against M. tuberculosis (MICs = 0.3-1.25 µg/ml). Ethionamide is a prodrug activated via oxidation by ethA (a flavin monooxygenase) and leading to the...
Reference: CDX-E0074-M250
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Potent immunosuppressant. Binds with high affinity to the FK506 binding protein-12 (FKBP-12) to generate an immunosuppressive complex that inhibits the...
Reference: CDX-E0074-M100
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Macrolide antibiotic, inhibiting bacterial protein synthesis. Potent immunosuppressant. Binds with high affinity to the FK506 binding protein-12 (FKBP-12) to generate an immunosuppressive complex that inhibits the...
Reference: CDX-D0356-G005
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D-cycloserine (DCS) is an antibiotic, inhibiting cell-wall biosynthesis in bacteria. It is a tuberculostatic agent, that inhibits L-alanine racemase and D-alanine:D-alanine ligase, enzymes essential to peptidoglycan...
Reference: CDX-D0356-G001
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D-cycloserine (DCS) is an antibiotic, inhibiting cell-wall biosynthesis in bacteria. It is a tuberculostatic agent, that inhibits L-alanine racemase and D-alanine:D-alanine ligase, enzymes essential to peptidoglycan...
Reference: CDX-C0702-M050
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Cryptochlorogenic acid (isomer of chlorogenic acid) is a phenolic acid found in various plant species, displaying diverse biological activities. It inhibits rat lens aldose reductase (RLAR) in vitro. Cryptochlorogenic...
Reference: CDX-C0702-M010
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Cryptochlorogenic acid (isomer of chlorogenic acid) is a phenolic acid found in various plant species, displaying diverse biological activities. It inhibits rat lens aldose reductase (RLAR) in vitro. Cryptochlorogenic...
Reference: CDX-C0361-M100
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Cefpodoxime is a metabolite of cefpodoxime proxetil, an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria (MIC90 ranges from 0.015-8 µg/ml). It is...
Reference: CDX-C0361-M025
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Cefpodoxime is a metabolite of cefpodoxime proxetil, an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria (MIC90 ranges from 0.015-8 µg/ml). It is...
Reference: CDX-C0339-M100
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Cordycepin is a nucleoside (adenosine analog) antibiotic that acts as a polyadenylation inhibitor when converted to 3’-deoxyadenosine triphosphate (3'-dATP), which inhibits ATP-dependent DNA and RNA synthesis....
Reference: CDX-C0339-M025
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Cordycepin is a nucleoside (adenosine analog) antibiotic that acts as a polyadenylation inhibitor when converted to 3’-deoxyadenosine triphosphate (3'-dATP), which inhibits ATP-dependent DNA and RNA synthesis....
Reference: CDX-C0339-M010
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Cordycepin is a nucleoside (adenosine analog) antibiotic that acts as a polyadenylation inhibitor when converted to 3’-deoxyadenosine triphosphate (3'-dATP), which inhibits ATP-dependent DNA and RNA synthesis....
Reference: CDX-C0310-M100
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Biologically incactive urinary metabolite of Clarithromycin (oxidized by ozone), a macrolide antibiotic. Compound can be used as analytical reference material.
Reference: CDX-C0310-M025
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Biologically incactive urinary metabolite of Clarithromycin (oxidized by ozone), a macrolide antibiotic. Compound can be used as analytical reference material.
Reference: CDX-C0310-M010
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Biologically incactive urinary metabolite of Clarithromycin (oxidized by ozone), a macrolide antibiotic. Compound can be used as analytical reference material.
Reference: CDX-C0058-M025
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Amine-reactive form of 6-carboxytetramethylrhodamine single isomer used for labeling of peptides and aminoglycoside antibiotics. It is also most commonly used in automated DNA sequencing.
Reference: CDX-C0058-M005
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Amine-reactive form of 6-carboxytetramethylrhodamine single isomer used for labeling of peptides and aminoglycoside antibiotics. It is also most commonly used in automated DNA sequencing.
Reference: CDX-B0302-M100
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Fluoroquinolone antibiotic with potent bactericidal activity. Inhibits the synthesis of bacterial DNA by interfering with the the supercoiling activity of DNA gyrase.
Reference: CDX-B0302-M025
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Fluoroquinolone antibiotic with potent bactericidal activity. Inhibits the synthesis of bacterial DNA by interfering with the the supercoiling activity of DNA gyrase.
Reference: CDX-B0144-G100
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Building block for synthesis. Key building block for synthesis of syringaldehyde (3,5-Dimethoxy-4-hydroxybenzaldehyde), which is a precursor of the widely spread antibiotic trimethoprim (TMP).
Reference: CDX-B0144-G025
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Building block for synthesis. Key building block for synthesis of syringaldehyde (3,5-Dimethoxy-4-hydroxybenzaldehyde), which is a precursor of the widely spread antibiotic trimethoprim (TMP).
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: 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-A0287-G005
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Broad-spectrum semisynthetic aminoglycoside antibiotic derived from kanamycin A, which is effective against Gram-negative and Gram-positive bacteria. Aminoglycoside antibiotics bind the 30s ribosomal subunit, causing...
Reference: CDX-A0197-GG25
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A tetracycline derivative exhibiting no antibiotic activity. A useful effector of tetracycline-dependent gene expression in bacterial expression systems.
Reference: CDX-A0197-M500
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A tetracycline derivative exhibiting no antibiotic activity. A useful effector of tetracycline-dependent gene expression in bacterial expression systems.
Reference: CDX-A0043-M020
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Biochemical/physiological actions: An antineoplastic antibiotic that inhibits cell proliferation by forming a stable complex with DNA and blocking the movement of RNA polymerase which interferes with DNA-dependent RNA...
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: BVT-L001-1
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The birch tree has been known for a long time for its healing properties in folk medicine. It can be expected that Betulin an active principle of the birch tree could be used for the treatment of various pathologies....
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: 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-0475-M001
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Macrolide antibiotic. Bafilomycin derivative, in which the characteristic hemiketal portion has been opened. Potent and specific vacuolar-type H+-ATPase inhibitor (V-ATPase). Antiproliferative agent against selected...
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-0472-M001
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Anthraquinone derivative derived from an angucyclinone precursor. Antibiotic. Antibacterial agent.
Reference: BVT-0470-M001
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C-glycosidic angucyclinone derivative. Antibiotic. Antitumor agent. Antibacterial agent. Isomer of fridamycin A (Prod. No. BVT-0469).
Reference: BVT-0469-M001
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C-glycosidic angucyclinone derivative. Antibiotic. Antitumor agent. Antibacterial agent. Isomer of fridamycin B (Prod. No. BVT-0470).
Reference: BVT-0468-M100
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Naturally occurring organosulfur compound. Osmolyte, osmoprotectant. Antioxidant. Cryoprotectant. Neuroprotective agent. Neuritogenic. Acts against immune-deficient diseases (e.g. cancer). Important in geochemistry,...
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
€0.00 (tax incl.)
Unique fungal allene derivative. Similar to A 82775C and iso-A 82775C. Biological activity not tested yet.
Reference: BVT-0466-M005
€0.00 (tax incl.)
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-0465-M005
€0.00 (tax incl.)
Mycotoxin. Phytotoxin. Shows cytotoxic, teratogenic, mutagenic and genotoxic properties by DNA intercalation. Induces several types of DNA damage, including oxidative DNA damage, single-stranded DNA breaks (SSB) and...
Reference: BVT-0465-M001
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Mycotoxin. Phytotoxin. Shows cytotoxic, teratogenic, mutagenic and genotoxic properties by DNA intercalation. Induces several types of DNA damage, including oxidative DNA damage, single-stranded DNA breaks (SSB) and...
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-0462-M010
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Hydroquinone antibiotic. Antibacterial and antifungal activity.
Reference: BVT-0462-M005
€0.00 (tax incl.)
Hydroquinone antibiotic. Antibacterial and antifungal activity.
Reference: BVT-0462-M001
€0.00 (tax incl.)
Hydroquinone antibiotic. Antibacterial and antifungal activity.
Reference: BVT-0461-M001
€0.00 (tax incl.)
Cytochalasan mycotoxin, derivative of chaetoglobosin A (Prod. No. BVT-0092 http://www.adipogen.com/bvt-0092/chaetoglobosin-a.html ). Phytotoxic. Cytotoxic against HCT116 (human colon cancer cells). Antibacterial (Ps....
Reference: BVT-0460-M001
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Cytochalasan mycotoxin, derivative of chaetoglobosin A (Prod. No. BVT-0092 http://www.adipogen.com/bvt-0092/chaetoglobosin-a.html ). Phytotoxic and antifungal compound. Moderate cytotoxic compound.
Reference: BVT-0458-M001
€0.00 (tax incl.)
Dimeric spiro-azaphilone. Mycotoxin.
Reference: BVT-0457-M001
€0.00 (tax incl.)
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-0456-M010
€0.00 (tax incl.)
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
€0.00 (tax incl.)
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-0455-M001
€0.00 (tax incl.)
Cyclodepsipeptide antibiotic. Unusual 12-membered macrocyclic depsipeptide comprises three unique subunits incorporating two substituted pyridines. Potent antitubercular agent. Inhibitor of NADH-dependent enoyl...
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-0453-M005
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Mycotoxin Antibacterial against Gram-positive bacteria. Shows antimalarial and antitubercular activity. Anticancer compound. Cytotoxic against several cancer cell lines (pro-apoptotic activity). Active against plant...
Reference: BVT-0452-M001
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Derivative of Aphidicolin (BVT-0307) http://www.adipogen.com/bvt-0307/-aphidicolin.html . Mycotoxin. So far no comparison to aphidicolin's biological activity (DNA polymerase alpha antiviral and antitumor activity)...
Reference: BVT-0452-C250
€0.00 (tax incl.)
Derivative of Aphidicolin (BVT-0307) http://www.adipogen.com/bvt-0307/-aphidicolin.html . Mycotoxin. So far no comparison to aphidicolin's biological activity (DNA polymerase alpha antiviral and antitumor activity)...

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