Cell Culture Media, Supplements, and Reagents
Bioworld Bialaphos, 500 mg
Naturally occurring antibiotic making it a particularly useful agent for selection in transformation research.Bialaphos is a natural herbicide produced by the bacteria Streptomyces hygroscopicus and Streptomyces viridochromegenes. Bialaphos is made of two alanine resudies and the glutamic acid analog phosphinothricin. It is commonly used as a gene selector in plants. Commonly used plasmids include: pGreenII 0229 and pGreenII 0229 62-SK.• Bialaphos Sodium Salt • Plant Tissue Culture TestedAppearance: SolidMelting Point: 160 °C
Medchemexpress LLC HY-12750 100mg , AZD3965 CAS:1448671-31-5 Purity:98%
Medchemexpress, HY-12750 100mg AZD3965 CAS:1448671-31-5 Formula:C21H24F3N5O5S Ki: 1.6 nM (MCT1) Purity:98% AZD3965 is a selective MCT1 inhibitor, it inhibits MCT1 with a binding affinity ( K i ) 1.6 nM and it is 6 fold selective over MCT2 and does not inhibit MCT3 or 4 at 10 μM concentrations. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC Bafilomycin B1 | 88899-56-3 | 1 MG
Bafilomycin B1 is a macrolide antibiotic isolated from mycelium of *Streptomyces gresuis*. It acts as a neuroprotective agent against Chloroquine-induced death and is a structural analog of Bafilomycin A1, capable of inhibiting V-ATPase. Bafilomycin B1 also significantly inhibits the oxidized low-density lipoprotein (LDL)-induced accumulation of lipid droplets.
- Significantly inhibits chloroquine-induced death of cerebellar granule neurons.
- Attenuates chloroquine-induced cell death in SH-SY5Y cells.
- Inhibits [14C]oleate incorporation into cholesteryl esters in J774 cells.
- Inhibits surface binding, intracellular accumulation, and degradation of oxidized 125I-LDL.
- Inhibits endosomal and lysosomal functions.
- Causes a reduction of cell surface receptors for oxidized LDL.
- Offers protection against α-synuclein-induced dopaminergic degeneration in worms.
Medchemexpress LLC Alamethicin | 27061-78-5 | 10 MG
Alamethicin is a linear 20-amino acid antibiotic that induces voltage-gated conductance in model and cell membranes. It exhibits antimicrobial activity against Gram-positive bacteria, but not Gram-negative bacteria. Alamethicin can form an amphipathic α-helical structure in biological membranes.
- Induces voltage-gated conductance in model and cell membranes.
- Exhibits antimicrobial activity against gram-positive bacteria.
- Forms an amphipathic α-helical structure in biological membranes.
- Possesses an unusual primary sequence with non-standard amino acids and modifications.
- Forms barrel-stave pores in model lipid multilayers.
Sigma Aldrich Fine Chemicals Biosciences Luliconazole >=98% (HPLC) | 187164-19-8 | MFCD00953915 | 50MG
Luliconazole >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 354.28 | 187164-19-8 | MFCD00953915 | 50MG
![Medchemexpress LLC 1,2-Ethanediamine, N1-[[3-[4,4-bis(ethoxymethyl)cyclohexyl]-1H-pyrazol-4-yl]methyl]-N1,N2-dimethyl | 1629013-22-4 | 99.4% | 366.54 g/mol | C20H38N4O2 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000262265.png-250.jpg)
Medchemexpress LLC 1,2-Ethanediamine, N1-[[3-[4,4-bis(ethoxymethyl)cyclohexyl]-1H-pyrazol-4-yl]methyl]-N1,N2-dimethyl | 1629013-22-4 | 99.4% | 366.54 g/mol | C20H38N4O2 | 5 MG
GSK3368715 (EPZ019997) is an orally active, reversible, S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferase (PRMT) inhibitor used for biochemical and cell-based research into arginine methylation and oncology-related pathways.
- Orally active, reversible type I PRMT inhibitor.
- SAM uncompetitive mechanism of action.
- Potent activity with low-nanomolar activity against PRMT1 and PRMT8.
- High purity (99.4% by HPLC) for research applications.
- Molecular formula C20H38N4O2; molecular weight 366.54 g/mol.
- Intended for in vitro and cellular research use only.
- Supplied in small research pack sizes suitable for screening and assays.
Medchemexpress LLC Huperzine B | 103548-82-9 | MFCD01716207 | 98.7% | 256.34 g/mol | C16H20N2O | 10 MG
Huperzine B is a Lycopodium alkaloid and a selective acetylcholinesterase (AChE) inhibitor used as a research reagent. It is supplied as a purified white to off-white solid with high purity and is suitable for biochemical and pharmacological studies.
- Selective acetylcholinesterase inhibitor.
- High purity (98.7%).
- White to off-white solid form.
- Available in milligram quantities and in DMSO solution for assays.
- Suitable for biochemical and pharmacological research applications.
Medchemexpress LLC Panobinostat | 404950-80-7 | MFCD09833242 | 10mg
Panobinostat | Purity: 99.20% | MW: 349.43 | 404950-80-7 | MFCD09833242 | 10mg
Sigma Aldrich Fine Chemicals Biosciences Lomustine Related Compound C United States Pharmacopeia (USP) Reference Standard | 2387-23-7 | MFCD00003829 | 25MG
Lomustine Related Compound C United States Pharmacopeia (USP) Reference Standard | Mol Wt: 224.34 | 2387-23-7 | MFCD00003829 | 25MG
Medchemexpress LLC HY-14229 5mg Medchemexpress, TGR5 Receptor Agonist CAS:1197300-24-5 Purity:>98%
Medchemexpress, HY-14229 5mg TGR5 Receptor Agonist CAS:1197300-24-5 TGR5 Receptor Agonist (CCDC), a potent TGR5(GPCR19) agonist, shows improved potency in the U2-OS cell assay (pEC50=6.8) and in melanophore cells (pEC50=7.5). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
eMolecules Medchem Express / Huperzine B / 5mg / 495802442 / HY-N2043 / / 103548-82-9 / MFCD01716207 / 256.349 / C16H20N2O
Medchem Express / Huperzine B / 5mg / 495802442 / HY-N2043 / / 103548-82-9 / MFCD01716207 / 256.349 / C16H20N2O
Medchemexpress LLC HY-19312 100mg Medchemexpress, 3-Methyladenine CAS:5142-23-4 Purity:>98%
Medchemexpress, HY-19312 100mg 3-Methyladenine CAS:5142-23-4 3-Methyladenine (3-MA) is a PI3K inhibitor. 3-Methyladenine is a widely used inhibitor of autophagy via its inhibitory effect on class III PI3K. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-17422 50mg Medchemexpress, Acyclovir CAS:59277-89-3 Purity:>98%
Medchemexpress, HY-17422 50mg Acyclovir CAS:59277-89-3 Acyclovir (Aciclovir) is a guanosine analogue and an orally active antiviral agent. Acyclovir inhibits HSV-1 (IC50 of 0.85 μM), HSV-2 (IC50 of 0.86 μM) and varicella-zoster virus. Acyclovir can be phosphorylated by viral thymidine kinase (TK), and Acyclovir triphosphate interferes with viral DNA polymerization through competitive inhibition with guanosine triphosphate and obligatory chain termination. Acyclovir prevents bacterial infections during induction therapy for acute leukaemia[4]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
AG Scientific Inc Valinomycin 100 MG
Valinomycin is an antibiotic which acts as a potassium (K+) ionophore. Induces K+ conductivity in cell membranes. Also active in vitro against Mycobacterium tuberculosis, and as an apoptosis inducer. Isolated from Streptomyces fulvissimus.Valinomycin is used diagnostically in ion selective electrodes because of its preferential ability to conduct K+ across the electrodes membrane. Valinomycin induced stimulation of mitochondrial energy dependent reversible swelling, supported by succinate oxidation, cytochrome c (cyto-c) and sulfite oxidase (Sox) (both are present in the mitochondrial intermembrane space (MIS)) are released outside.Valinomycin also inhibits hyphal growth in other dimorphic fungi, Candida tropicalis and Aureobasidium pullulan. It affects the morphology of Candida albicans.
eMolecules AstaTech / SR9009 / 0.25g / 411869817 / 40199 / 97.000 / 1379686-30-2 / MFCD29472236 / 437.940 / C20H24ClN3O4S
AstaTech / SR9009 / 0.25g / 411869817 / 40199 / 97.000 / 1379686-30-2 / MFCD29472236 / 437.940 / C20H24ClN3O4S