Pyrroles
Medchemexpress LLC Varespladib methyl | 172733-08-3 | 99.9% | 394.42 g/mol | C22H22N2O5 | 10 MG
Varespladib methyl is a small-molecule research compound that selectively inhibits group II secretory phospholipase A2 (sPLA2). It is supplied as a high-purity solid for biochemical and pharmacological studies, and is commonly used in in vitro enzyme inhibition assays, mechanistic studies of inflammatory pathways, and preclinical research on venom neutralization.
- Selective inhibitor of group II secretory phospholipase A2 (sPLA2).
- High purity suitable for research use (reported 99.90%).
- Molecular formula C22H22N2O5; molecular weight 394.42 g/mol.
- Available in small vial sizes for laboratory workflows.
- Suitable for in vitro assays and preclinical studies involving PLA2 pathways.
Medchemexpress LLC HY-12981 5mg Medchemexpress, RG7713 CAS:920022-47-5 Purity:>98%
Medchemexpress, HY-12981 5mg RG7713 CAS:920022-47-5 RG7713 (RO5028442) is a highly potent and selective Brain-Penetrant Vasopressin 1a (V1a) receptor antagonist with Kis of 1 nM (hV1a) and 39 nM (mV1a). 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-B0002A 50mg Medchemexpress, Ondansetron (hydrochloride dihydrate) CAS:103639-04-9 Purity:>98%
Medchemexpress, HY-B0002A 50mg Ondansetron (hydrochloride dihydrate) CAS:103639-04-9 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-U00070 1mg Medchemexpress, Dirlotapide CAS:481658-94-0 Purity:>98%
Medchemexpress, HY-U00070 1mg Dirlotapide CAS:481658-94-0 Dirlotapide (CP742033) is a gut-selective inhibitor of microsomal triglyceride transfer protein (MTP) that reliably produces weight loss in obese dogs. 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.
Selleck Chemical LLC Ac-YVAD-cmk-5mg
Ac-YVAD-cmk (Caspase-1 Inhibitor II) is a selective IL-1β converting enzyme (ICE) inhibitor with neuroprotective and anti-inflammatory effects, effectively suppresses the expression of IL-1β and IL-18.
Selleck Chemical LLC 1-Furfurylpyrrole
1-Furfurylpyrrole (N-Furfurylpyrrole) is a potential contributor of flavor and aroma to popcorn
Medchemexpress LLC Cevidoplenib dimesylate | 2043659-93-2 | 99.0% | 665.74 | 1 ML
Cevidoplenib is an orally available inhibitor of spleen tyrosine kinase (Syk), with potential anti-inflammatory and immunomodulating activities.
- Orally available inhibitor of spleen tyrosine kinase (Syk).
- Possesses potential anti-inflammatory activities.
- Exhibits potential immunomodulating activities.
eMolecules 66635-93-6 | Medchem Express | (R)-Ketorolac | 5mg | 482204529 | HY-B0580B | MFCD00871492 | 255.273 | C15H13NO3
Medchem Express | (R)-Ketorolac | 5mg | 482204529 | HY-B0580B | 66635-93-6 | MFCD00871492 | 255.273 | C15H13NO3
Medchemexpress LLC Quiflapon (MK-591) | 136668-42-3 | 99.4% | 587.2 g/mol | C34H35ClN2O3S | 100 MG
Quiflapon (MK-591) is a selective and specific 5-lipoxygenase-activating protein (FLAP) inhibitor used in research to study leukotriene biosynthesis and FLAP-mediated pathways. It demonstrates high potency (IC50 = 1.6 nM in a FLAP binding assay) and is supplied as a high-purity analytical standard for assay development and in vitro studies.
- Selective FLAP inhibition with IC50 = 1.6 nM.
- High purity (99.44%) suitable for analytical use.
- Available in multiple formats, including 10 mM solution and 5 mg-100 mg solid quantities.
- Intended for research and assay development applications.
eMolecules 880813-36-5 | Medchem Express | PhiKan 083 | 5mg | 441681796 | HY-108637 | MFCD07366384 | 238.334 | C16H18N2
Medchem Express | PhiKan 083 | 5mg | 441681796 | HY-108637 | 880813-36-5 | MFCD07366384 | 238.334 | C16H18N2
Medchemexpress LLC JNJ-63576253 | 50MG
JNJ-63576253 (TRC-253) is a potent and orally active full antagonist of androgen receptor (AR) with IC50s of 37 and 54 nM for F877L mutant AR and wild-type AR in LNCaP cells JNJ-63576253 can be used for the research of castration-resistant prostate cancer (CRPC)[1]
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 Mutated EGFR-IN-1 (osimertinib analog) | 1421372-66-8 | 99.9% | C25H31N7O | 500 MG
Mutated EGFR-IN-1 (osimertinib analog) | 1421372-66-8 | 99.9% | C25H31N7O | 500 MG