Category: Reagents

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-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-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-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-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-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-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: 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: 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-A0197-GG25
€0.00 (tax incl.)
A tetracycline derivative exhibiting no antibiotic activity. A useful effector of tetracycline-dependent gene expression in bacterial expression systems.
Reference: CDX-A0287-G005
€0.00 (tax incl.)
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-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-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-A0298-M025
€0.00 (tax incl.)
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-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-B0144-G025
€0.00 (tax incl.)
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-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-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-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-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-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-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-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-M100
€0.00 (tax incl.)
Biologically incactive urinary metabolite of Clarithromycin (oxidized by ozone), a macrolide antibiotic. Compound can be used as analytical reference material.
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-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-M100
€0.00 (tax incl.)
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-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-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-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-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-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-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-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-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-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-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-G100
€0.00 (tax incl.)
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-E0574-M001
€0.00 (tax incl.)
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-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-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-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-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-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-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-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-GG25
€0.00 (tax incl.)
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-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-J0009-L005
€0.00 (tax incl.)
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
€0.00 (tax incl.)
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-L005
€0.00 (tax incl.)
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-L0031-M025
€0.00 (tax incl.)
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...

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...

IDA

Reference: CDX-M0001-M025
€0.00 (tax incl.)
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-M250
€0.00 (tax incl.)
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-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.
Reference: CDX-M0091-G001
€0.00 (tax incl.)
A main acid metabolite of the antibiotic metronidazole showing some antibacterial activity. Compound can be used as analytical reference material.
Reference: CDX-M0161-M005
€0.00 (tax incl.)
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
€0.00 (tax incl.)
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-M025
€0.00 (tax incl.)
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-M0189-M050
€0.00 (tax incl.)
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-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-S0056-M025
€0.00 (tax incl.)
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-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-S0267-G010
€0.00 (tax incl.)
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-G025
€0.00 (tax incl.)
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-T0096-G005
€0.00 (tax incl.)
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-G025
€0.00 (tax incl.)
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-0253-M001
€0.00 (tax incl.)
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-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....

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