Oxazoles
Medchemexpress LLC 4-(Chloromethyl)-7-hydroxycoumarin | 25392-41-0 | 98.0% | C10H7ClO3 | 250 MG
4-(Chloromethyl)-7-hydroxycoumarin is a hydroxycoumarin derivative exhibiting potent antioxidant effects and high hydroxyl radical-scavenging properties. It contains a methyl group and a chlorine group within its heterocyclic ring. This compound has been investigated for its ability to inhibit the zinc enzyme carbonic anhydrase, particularly tumor-associated isoforms CA IX and XII.
- Exhibits potent antioxidant effect
- Possesses high hydroxyl radical-scavenging property
- Contains methyl and chlorine groups in the heterocyclic ring
- Investigated as an inhibitor of zinc enzyme carbonic anhydrase
- Targets tumor-associated isoforms CA IX and XII
- For research use only
Chem Service Inc TERBUTRYNE 250MG
This item has a minimum order quantity of 2 per supplier requirements
Medchemexpress LLC Ethyl oxazole-4-carboxylate | 23012-14-8 | >99.9% | C6H7NO3 | 25 G
Ethyl oxazole-4-carboxylate is a biochemical reagent suitable for life science related research. It serves as a biological material or organic compound for laboratory applications and substance manufacturing. This product is for research use only and not intended for medical applications or patient use.
- Biochemical reagent for life science research
- High purity (>99.9%)
- Solid appearance, light yellow to yellow color
- Stable in powder form: store at -20°C for 3 years or 4°C for 2 years
- Stable in solvent: store at -80°C for 6 months or -20°C for 1 month
- Melting point of 48°C
- Boiling point of 202°C at 760 mmHg
Medchemexpress LLC Dimethyl octadecaned 5g
Dimethyl octadecanedioate (Octadecanedioic acid dimethyl ester) is an ester product
eMolecules 5-Phenyl-oxazol-2-ylamine | 6826-24-0 | MFCD00087876 | 5g
J & W PharmLab LLC | 5-Phenyl-oxazol-2-ylamine | 5g | 289353109 | 56R0018 | 96.000 | 6826-24-0 | MFCD00087876 | 160.176 | C9H8N2O
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eMolecules Building Block Tool
Ethos Biosciences Cytoplasmic Counterstain Histology Cytology 1/EA
Eosin Y Intensified is a ready-to-use cytoplasmic counterstain formulated to provide enhanced staining intensity in routine histology and cytology applications Designed for use in hematoxylin and eosin (H E) procedures it produces deeper pink to red coloration of cytoplasm connective tissue and extracellular components improving contrast and tissue definition The intensified formulation supports consistent color development and is suitable for manual or automated staining systems Ideal for clinical research and educational laboratories Eosin Y Intensified delivers reliable reproducible results for routine tissue evaluation and morphology studies
Medchemexpress LLC An-12-H5 intermediate-3 | 851314-03-9 | 95.8% | 330.18 g/mol | C13H16BrNO4 | 500 MG
AN-12-H5 intermediate-3 is a chemical intermediate used to synthesize the antiviral inhibitor AN-12-H5 and as a building block for antibody-drug conjugate (ADC) development. The material is supplied for research use and is characterized by reported purity, molecular identifiers, and supplier storage recommendations.
- High reported purity of 95.8%.
- Molecular formula C13H16BrNO4 and molecular weight 330.18 g/mol.
- Suitable as a building block for antiviral compound synthesis and ADC conjugation.
- Available in research pack sizes including 500 mg.
- Recommended storage: powder at -20°C for long-term, 4°C for short-term.
Medchemexpress LLC 1-(4-methoxyphenyl)-3-methyl-1H-pyrazol-5(4H)-one | 60798-06-3 | MFCD01361012 | 99.5% | 204.22 g/mol | C11H12N2O2 | 250 MG
- reported antiprion activity in ScN2a and F3 cell assays (IC50 ~13 nM and 25 nM)
- high chemical purity suitable for biological assays
- well-defined molecular identity (CAS 60798-06-3, C11H12N2O2)
- commonly used in small-molecule screening and neurodegeneration research
Medchemexpress LLC 2-Pyrrolidinone, 5-[(3S)-3-hydroxy-4-phenyl-1-buten-1-yl]-1-[6-(2H-tetrazol-5-yl)hexyl]- | 346673-06-1 | 98.3% | 383.49 | 50 MG
TCS 2510 is a selective EP4 agonist and can be used for the research of metabolic diseases. It stimulates glucagon-like peptide 1 and 2 secretion, activates the Gas signaling pathway, and increases Gcg mRNA expression levels. In vivo studies show it elevates plasma glucagon-like peptide 1 and 2 levels in mice.
- Stimulates glucagon-like peptide 1 secretion.
- Activates the Gas signaling pathway.
- Increases Gcg mRNA expression levels.
- Produces a concentration-dependent increase in cAMP levels in GLUTag cells.
- Decreases cell impedance in GLUTag cells.
- Produces a concentration-dependent increase in glucagon-like peptide 2 secretion.
- Elevates plasma glucagon-like peptide 1 levels in fasted mice.
- Increases plasma glucagon-like peptide 2 levels in mice.
Selleck Chemical LLC Y-27632
Y-27632 is a selective ROCK1 and ROCK2 inhibitor with a Ki of 140 nM and 300nM in a cell-free assay exhibits 200-fold selectivity over other kinases including PKC cAMP-dependent protein kinase MLCK and PAK
![Medchemexpress LLC N-(octahydrobenzo[e]pyrido[1,2-a]diazepin-8-yl)thiophene-2-sulfonamide | 1193340-31-6 | 98.0% | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000230745.png-250.jpg)
Medchemexpress LLC N-(octahydrobenzo[e]pyrido[1,2-a]diazepin-8-yl)thiophene-2-sulfonamide | 1193340-31-6 | 98.0% | 10 MG
AN-12-H5 is a small-molecule antienterovirus research compound that inhibits replication of poliovirus (PV) and enterovirus 71 (EV71). It is supplied as a solid or as a DMSO solution and is intended for laboratory research use only.
- Targets viral replication of PV and EV71.
- High purity (≈98%).
- Soluble in DMSO (100 mg/mL); ultrasonic recommended.
- Provided as solid or pre-dissolved DMSO solution for convenient use in assays.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC Y-33075 dihydrochloride | 173897-44-4 | 98.0% | 353.25 | C16H18Cl2N4O | 100 MG
A potent, selective Rho-associated protein kinase (ROCK) inhibitor supplied as the dihydrochloride salt for research use, suitable for cellular and biochemical assays.
- Selective Rho-associated protein kinase (ROCK) inhibition with an IC50 of 3.6 nM.
- High purity (98.02%), appropriate for preclinical research applications.
- Well-characterized chemical identity: C16H18Cl2N4O, MW 353.25, CAS 173897-44-4.
- Available in multiple pack sizes, including 100 MG, for experimental flexibility.
- Accompanied by datasheet and batch-specific certificate of analysis for quality assurance.