Pyrroles
Cayman Chemical SBromoenol lactone
A selective iPLA2β inhibitor; inhibits vasopressin-induced release of arachidonate from cultured rat aortic smooth muscle (A10) cells (IC50 = 2 µM); >1,000-fold selective for iPLA2 versus cPLA2 and 10-fold selective for iPLA2β versus iPLA2γ
eMolecules Medchem Express / Bazedoxifene / 5mg / 415688411 / HY-A0031 / / 198481-32-2 / MFCD05148441 / 470.613 / C30H34N2O3
Medchem Express / Bazedoxifene / 5mg / 415688411 / HY-A0031 / / 198481-32-2 / MFCD05148441 / 470.613 / C30H34N2O3
Medchemexpress LLC 1-phenylpyrrole | 635-90-5 | MFCD00005343 | 99.9% | 143.19 g/mol | C10H9N | 5G
1-Phenylpyrrole is a small organic compound that exhibits polarity-dependent dual fluorescence, showing a single emission band in nonpolar solvents and a red-shifted band in polar solvents. It is supplied as a solid and as a concentrated DMSO solution for use in photophysical and fluorescence studies.
- Exhibits dual fluorescence dependent on solvent polarity.
- High purity (99.94%) suitable for research applications.
- Molecular formula C10H9N; molecular weight 143.19 g/mol.
- Available as solid and 10 mM solution in DMSO; DMSO solubility 100 mg/mL.
- Physical appearance: light yellow to light brown solid.
- Storage: powder at -20°C (up to 3 years) or 4°C (up to 2 years); stock solutions at -80°C (6 months).
- Intended for fluorescence and solvent-dependent photophysical investigations.
Apexbio Technology LLC Bromoenol lactone 88070-98-8 10mg
Bromoenol lactone (CAS 88070-98-8) is an irreversible inhibitor of cytosolic calcium-independent phospholipase A2 (iPLA2) an enzyme involved in the regulation of arachidonic acid release and lysophospholipid production iPLA2 activity is associated with phospholipid remodeling and the generation of signaling molecules that modulate processes such as eicosanoid synthesis insulin secretion apoptosis and cellular proliferation In cellular assays bromoenol lactone induces apoptosis in various cell lines and promotes proteolysis of procaspase-9 and procaspase-3 It also inhibits phosphatidic acid phosphohydrolase activity and disrupts triacylglycerol biosynthesis in macrophage models Bromoenol lactone is widely utilized in studies investigating lipid signaling cell death mechanisms and metabolic pathways
Medchemexpress LLC Pitavastatin lactone | 141750-63-2 | 99.3% | 403.45 g/mol | C25H22FNO3 | 25MG
Pitavastatin lactone is the lactone metabolite of pitavastatin, provided as a high-purity analytical standard for in vitro and metabolic studies. The material is supplied as a white to off-white solid with specified solubility in DMSO and recommended low-temperature storage to preserve stability and integrity for analytical workflows.
- High purity: 99.3%.
- Molecular formula: C25H22FNO3; molecular weight: 403.45 g/mol.
- Appearance: white to off-white solid.
- Solubility: DMSO 100 mg/mL; ultrasonic assistance recommended.
- Storage: powder at -20°C (stable up to 3 years); in solvent -80°C for 6 months or -20°C for 1 month.
- Supplied in small pack sizes suitable for analytical testing.
- For research use only; not for human or clinical use.
Medchemexpress LLC HY-101971 5mg Medchemexpress, AZ PFKFB3 26 CAS:1704740-52-2 Purity:>98%
Medchemexpress, HY-101971 5mg AZ PFKFB3 26 CAS:1704740-52-2 AZ PFKFB3 26 is a potent and selective inhibitor of the metabolic kinase PFKFB3 with an IC50 of 23 nM. AZ PFKFB3 26 inhibits PFKFB1 and PFKFB2 with IC50s of 2.06 and 0.384 μM, respectively. 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 L-Gulono-1,4-lactone | 1128-23-0 | MFCD00064331 | 178.14 g/mol | C6H10O6 | 1 ML
L-Gulono-1,4-lactone is an endogenous metabolite and precursor to ascorbic acid, supplied as a 10 mM aqueous solution (1 mL) intended for research and analytical applications. It is provided as an analytical standard for qualitative and quantitative assays and is compatible with HPLC, GC, and MS workflows.
- Analytical standard quality suitable for HPLC, GC, and MS
- Provides a stable precursor for ascorbic acid biosynthesis studies
- Ready-to-use aqueous solution for convenient experimental setup
- Small vial volume minimizes waste for low-volume assays
- Intended for research and analytical applications
eMolecules 3-Bromo-6-ethoxy-2-fluorophenylboronic acid | 1309980-98-0 | MFCD12026724 | 1g
Combi-Blocks | 3-Bromo-6-ethoxy-2-fluorophenylboronic acid | 1g | 482931609 | FA-3805 | 95.000 | 1309980-98-0 | MFCD12026724 | 262.870 | C8H9BBrFO3
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Medchemexpress LLC Az PFKFB3 26 | 1704740-52-2 | MFCD30742931 | 98.3% | 402.49 | C24H26N4O2 | 25 MG
AZ PFKFB3 26 is a potent, selective small-molecule inhibitor of PFKFB3 used in research on glycolytic regulation and cancer metabolism. It displays low-nanomolar biochemical potency and measurable cellular effects in tumor cell assays, and is provided as a high-purity solid for laboratory use.
- Potent PFKFB3 biochemical inhibitor (IC50 23 nM).
- Selective over PFKFB1 and PFKFB2 (IC50s 2.06 μM and 0.384 μM).
- Active in A549 cells (fructose-1,6-bisphosphate reduction IC50 0.343 μM).
- High-purity research-grade material suitable for in vitro studies.
- Available in small pack sizes for preclinical experiments.
Medchemexpress LLC Atorvastatin methyl ester | 345891-62-5 | MFCD21363420 | 98.8% | C34H37FN2O5 | 10MG
Atorvastatin methyl ester is a methyl-esterified derivative of atorvastatin provided for laboratory research. It is used as a drug derivative and has been reported to inhibit 9-cis-RA-induced Gal4 reporter activity more strongly than atorvastatin. The compound is supplied as solids and as a DMSO solution for in vitro experiments.
- Methyl-esterified derivative of atorvastatin used for research
- Reported to inhibit 9-cis-RA-induced Gal4 reporter activity more strongly than atorvastatin
- Available as solid quantities (10 mg-500 mg) and 10 mM solution in DMSO
- High purity (approx. 98.8%) suitable for in vitro studies
- Useful structural analogue for metabolism and activity studies
Medchemexpress LLC HY-19889 5mg Medchemexpress, JNJ-18038683 CAS:851376-05-1 Purity:>98%
Medchemexpress, HY-19889 5mg JNJ-18038683 CAS:851376-05-1 JNJ-18038683 is a 5-Hydroxytryptamine Type 7 (5-HT7) receptor antagonist, with pKis of 8.19, 8.20 for rat and human 5-HT7 in HEK293 cells, respectively. 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.