Category: Reagents

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-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
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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-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
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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-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
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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-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
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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-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-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-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
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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-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
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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-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
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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-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: 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: 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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