Benzopyrans
TARGETMOL CHEMICALS INC DEGUELIN 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Deguelin ((-)-Deguelin) is a PI3K/AKT Inhibitor which is a natural product isolated from plants in the Mundulea sericea family. purity: 98%
Medchemexpress LLC Iclaprim | 192314-93-5 | MFCD09837803 | >98.0% | 354.40 g·mol⁻¹ | C19H22N4O3 | 10 MG
Iclaprim is a diaminopyrimidine antibiotic that inhibits bacterial dihydrofolate reductase and is active against Gram-positive organisms, including methicillin-resistant Staphylococcus aureus (MRSA). Supplied as a 10 mg research reagent, it is intended for in vitro studies and preclinical research. Molecular formula C19H22N4O3; molecular weight 354.40 g·mol⁻¹.
- Potent inhibitor of bacterial dihydrofolate reductase.
- Active against MRSA with reported MIC90 of 0.06 μg/mL.
- Provided as a small-scale research sample for in vitro assays.
- Well characterized chemically with defined formula and molecular weight.
- Purity commonly reported as >98% by HPLC in supplier listings.
Medchemexpress LLC Iclaprim | 192314-93-5 | MFCD09837803 | 98.9% | 354.40 g/mol | C19H22N4O3 | 1 ML
Iclaprim is a selective bacterial dihydrofolate reductase inhibitor used in research on Gram-positive organisms. It shows activity against Staphylococcus aureus, including MRSA, with a reported MIC90 of 0.06 μg/mL. The compound is supplied as a high-purity research reagent and is commonly provided as a 10 mM solution in DMSO for in vitro assays.
- High purity (98.9%).
- Active against Staphylococcus aureus, including MRSA (MIC90 0.06 μg/mL).
- Provided as a 10 mM solution in DMSO (1 mL) for in vitro studies.
- Recommended solvent DMSO; may require warming and sonication to dissolve.
- Molecular weight 354.40 g/mol; formula C19H22N4O3.
- Storage conditions available for powder and in-solution forms to preserve stability.
Medchemexpress LLC Iclaprim | 192314-93-5 | MFCD09837803 | 98.9% | 354.40 g/mol | C19H22N4O3 | 100 MG
Iclaprim is a bacterial dihydrofolate reductase inhibitor supplied as a research-grade powder for analytical and laboratory use. It demonstrates potent activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus, with a reported MIC90 of 0.06 μg/mL. Molecular formula C19H22N4O3; molecular weight 354.40 g/mol.
- Research-grade powder form for laboratory assays.
- High stated purity of 98.9% for reliable analytical results.
- Potent activity against Staphylococcus aureus (MRSA).
- Suitable as a reference standard or tool compound in microbiology studies.
- Available in 100 mg quantity for small-scale experiments.
Sigma Aldrich Fine Chemicals Biosciences (-)-Deguelin >98% (HPLC), powder | Purity: >98% (HPLC) | Mol Wt: 394.42 | 522-17-8 | MFCD01740600 | 5MG
(-)-Deguelin >98% (HPLC), powder | Purity: >98% (HPLC) | Mol Wt: 394.42 | 522-17-8 | MFCD01740600 | 5MG
Cayman Chemical Deguelin Enzyme Inhibitors
A rotenoid with diverse biological activities; inhibits mitochondrial complex I activity in bovine heart electron transport particles and phorbol 12-myristate 13-acetate-induced ODC activity in MCF-7 cells (IC50s = 6.9 and 11 nM, respectively); induces apoptosis in MCF-7 and SK-BR-3 cells at 100 nM; induces mortality in adult bruchid beetles (C. maculatus) from 10-500 ppm; induces nigrostriatal dopaminergic degeneration in rats at 6 mg/kg
Selleck Chemical LLC Deguelin
Deguelin a natural product isolated from plants in the Mundulea sericea family is an PI3K/AKT Inhibitor
AdipoGen Citrinin
Chemical. CAS 518-75-2. Formula C13H14O5. MW 250.3. Isolated from Penicillium citrinum strain FKI-4836. Antibiotic. Antiprotozoal. Antimicrobial. Cytotoxic and genotoxic in various mammalian cells. Mitochondrial permeability transition pore MPTP activator. Apoptosis inducer. ERK and JNK signaling pathways activator. Nephrotoxic mycotoxin. Suppresses NO and iNOS expression via inhibition of the JAK/STAT-1alpha and NF-kappaB signaling pathways. Tubulin polymerization and mitotic spindle assembly inhibitor. Increases reactive oxygen species ROS. Induces cell cycle arrest at the G0/G1 and G2/M phase.
Cayman Chemical Deguelin Enzyme Inhibitors
A rotenoid with diverse biological activities; inhibits mitochondrial complex I activity in bovine heart electron transport particles and phorbol 12-myristate 13-acetate-induced ODC activity in MCF-7 cells (IC50s = 6.9 and 11 nM, respectively); induces apoptosis in MCF-7 and SK-BR-3 cells at 100 nM; induces mortality in adult bruchid beetles (C. maculatus) from 10-500 ppm; induces nigrostriatal dopaminergic degeneration in rats at 6 mg/kg
Sigma Aldrich Fine Chemicals Biosciences Citrinin from Penicillium citrinum, >=98% (HPLC) | 518-75-2 | MFCD00006912 | 5MG
Citrinin from Penicillium citrinum, >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 250.25 | 518-75-2 | MFCD00006912 | 5MG
![Medchemexpress LLC Spiro[2H-1-benzopyran-2,4'-[4H]pyran], 2',3',5',6'-tetrahydro-6,7-bis[(4-nitrophenyl)methoxy]- | 2109805-75-4 | MFCD31692328 | 99.0% | 504.49 g/mol | C27H24N2O8 | 1 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000245852.png-250.jpg)
Medchemexpress LLC Spiro[2H-1-benzopyran-2,4'-[4H]pyran], 2',3',5',6'-tetrahydro-6,7-bis[(4-nitrophenyl)methoxy]- | 2109805-75-4 | MFCD31692328 | 99.0% | 504.49 g/mol | C27H24N2O8 | 1 MG
CU-CPT17e is a potent multi-Toll-like receptor (TLR) agonist used in research to activate TLR3, TLR8, and TLR9. It is provided as a high-purity small molecule for in vitro pharmacology and mechanistic studies.
- Potent multi-TLR agonist activating TLR3, TLR8, and TLR9.
- High purity (99.0%), suitable for research applications.
- Molecular weight 504.49 g/mol, formula C27H24N2O8.
- Soluble in DMSO for standard laboratory assays.
- Available in multiple pack sizes, including 1 mg screening quantities.
- Intended for in vitro pharmacology and mechanistic studies.
Selleck Chemical LLC Deguelin
Deguelin a natural product isolated from plants in the Mundulea sericea family is an PI3K/AKT Inhibitor