Category: Reagents

Filter By
Reference: A1922-25
€0.00 (tax incl.)
Caspase-2 inhibitor
Reference: BVT-0091-M001
€0.00 (tax incl.)
Antibiotic. Apoptosis and endoplasmic reticulum stress-mediated cell death inducer. Potent, selective and competitive cell permeable rasfarnesyltransferase inhibitor (IC50 = 30 nM). Does not affect...
Reference: 11622-1
€0.00 (tax incl.)
A prodrug formulation of HPA which may be useful in various biochemical studies and as a reference standard in analytical work
Reference: A1923-S
€0.00 (tax incl.)
Caspase-6 inhibitor
Reference: BVT-0091-M005
€0.00 (tax incl.)
Antibiotic. Apoptosis and endoplasmic reticulum stress-mediated cell death inducer. Potent, selective and competitive cell permeable rasfarnesyltransferase inhibitor (IC50 = 30 nM). Does not affect...
Reference: 11622-10
€0.00 (tax incl.)
A prodrug formulation of HPA which may be useful in various biochemical studies and as a reference standard in analytical work
Reference: A1923-1
€0.00 (tax incl.)
Caspase-6 inhibitor
Reference: BVT-0091-M010
€0.00 (tax incl.)
Antibiotic. Apoptosis and endoplasmic reticulum stress-mediated cell death inducer. Potent, selective and competitive cell permeable rasfarnesyltransferase inhibitor (IC50 = 30 nM). Does not affect...
Reference: 11622-5
€0.00 (tax incl.)
A prodrug formulation of HPA which may be useful in various biochemical studies and as a reference standard in analytical work
Reference: A1923-5
€0.00 (tax incl.)
Caspase-6 inhibitor
Reference: BVT-0092-M001
€0.00 (tax incl.)
Antibiotic. Cytochalasan analog with anti-fungal activity. Phytotoxic, nematicidal and anti-bacterial activity. Exhibits cytotoxic effects against human cancer cell lines. Induces apoptosis in lymphocytic leukemia...
Reference: 11910-100
€0.00 (tax incl.)
Base treatment of human seminal plasma extracts converts the 19-hydroxy PGE compounds present in the sample into the corresponding PGB compounds generating strong conjugated dienone chromophores. This method has been...
Reference: A1923-10
€0.00 (tax incl.)
Caspase-6 inhibitor
Reference: BVT-0092-M005
€0.00 (tax incl.)
Antibiotic. Cytochalasan analog with anti-fungal activity. Phytotoxic, nematicidal and anti-bacterial activity. Exhibits cytotoxic effects against human cancer cell lines. Induces apoptosis in lymphocytic leukemia...
Reference: 11910-50
€0.00 (tax incl.)
Base treatment of human seminal plasma extracts converts the 19-hydroxy PGE compounds present in the sample into the corresponding PGB compounds generating strong conjugated dienone chromophores. This method has been...
Reference: A1923-25
€0.00 (tax incl.)
Caspase-6 inhibitor
Reference: BVT-0095-M001
€0.00 (tax incl.)
Antibiotic. Shows weak cytotoxic activity against different tumor cell lines. Shows antiparasitic activity.
Reference: 11910-500
€0.00 (tax incl.)
Base treatment of human seminal plasma extracts converts the 19-hydroxy PGE compounds present in the sample into the corresponding PGB compounds generating strong conjugated dienone chromophores. This method has been...
Reference: A1924-1
€0.00 (tax incl.)
Caspase 5 inhibitor,potent,cell-permeable and irreversible
Reference: BVT-0097-M001
€0.00 (tax incl.)
Phytotoxin. Microtubule assembly inhibitor. Similar to curvularin.
Reference: 12210-1
€0.00 (tax incl.)
The trans isomer of PGD2 occurs as an impurity between 2-5% in most commercial preparations of the bulk drug product. This compound was prepared primarily as an analytical standard for detection and quantitation of...
Reference: A1924-5
€0.00 (tax incl.)
Caspase 5 inhibitor,potent,cell-permeable and irreversible
Reference: BVT-0098-C500
€0.00 (tax incl.)
Macrolide antibiotic. Bacterial, protozoan and mammalian threonyl-tRNA synthetase (THrRS) inhibitor. Antiangiogenic (IC50 = 0.8 nM) and anticancer agent. Induces the collapse of formed capillary tubes in a...
Reference: 12210-10
€0.00 (tax incl.)
The trans isomer of PGD2 occurs as an impurity between 2-5% in most commercial preparations of the bulk drug product. This compound was prepared primarily as an analytical standard for detection and quantitation of...
Reference: BVT-0098-M001
€0.00 (tax incl.)
Macrolide antibiotic. Bacterial, protozoan and mammalian threonyl-tRNA synthetase (THrRS) inhibitor. Antiangiogenic (IC50 = 0.8 nM) and anticancer agent. Induces the collapse of formed capillary tubes in a...
Reference: 12210-5
€0.00 (tax incl.)
The trans isomer of PGD2 occurs as an impurity between 2-5% in most commercial preparations of the bulk drug product. This compound was prepared primarily as an analytical standard for detection and quantitation of...
Reference: BVT-0098-M005
€0.00 (tax incl.)
Macrolide antibiotic. Bacterial, protozoan and mammalian threonyl-tRNA synthetase (THrRS) inhibitor. Antiangiogenic (IC50 = 0.8 nM) and anticancer agent. Induces the collapse of formed capillary tubes in a...
Reference: 13006-1
€0.00 (tax incl.)
A synthetic intermediate useful for pharmaceutical synthesis
Reference: BVT-0099-C250
€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.
Reference: 13006-250
€0.00 (tax incl.)
A synthetic intermediate useful for pharmaceutical synthesis
Reference: BVT-0099-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.
Reference: 13006-500
€0.00 (tax incl.)
A synthetic intermediate useful for pharmaceutical synthesis
Reference: BVT-0100-C250
€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...
Reference: 13006-5
€0.00 (tax incl.)
A synthetic intermediate useful for pharmaceutical synthesis
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...
Reference: 13048-1
€0.00 (tax incl.)
Contains a 50 µg vial of EPA-d5 and a precisely weighed vial of unlabeled EPA (weight provided on the vial) for the convenient, precise quantification of EPA by GC- or LC-MS
Reference: A1926-S
€0.00 (tax incl.)
Cathepsin B inhibitor
Reference: BVT-0107-C500
€0.00 (tax incl.)
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: A1926-1
€0.00 (tax incl.)
Cathepsin B inhibitor
Reference: BVT-0107-M001
€0.00 (tax incl.)
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: A1926-5
€0.00 (tax incl.)
Cathepsin B inhibitor
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: A1926-5.1
€0.00 (tax incl.)
Cathepsin B inhibitor
Reference: BVT-0112-M005
€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: 2110001
€0.00 (tax incl.)
research grade
Reference: A1926-10
€0.00 (tax incl.)
Cathepsin B inhibitor
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: 2110002
€0.00 (tax incl.)
research grade
Reference: A1926-25
€0.00 (tax incl.)
Cathepsin B inhibitor
Reference: BVT-0139-C250
€0.00 (tax incl.)
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...

Menu

Settings