Thiophenes
eMolecules 21314-77-2 | (3-Pyridyl)-thiophen-2-yl-methanol | Chem-Impex | MFCD01108848 | 191.250 | C10H9NOS | 95.000 | OC(c1cccs1)c1cccnc1 | 250mg | 449074524
(3-Pyridyl)-thiophen-2-yl-methanol | Chem-Impex | 21314-77-2 | MFCD01108848 | 191.250 | C10H9NOS | 95.000 | OC(c1cccs1)c1cccnc1 | 250mg | 449074524
![eMolecules 21222-61-7 | 1-(2-Aminobenzo[d]thiazol-6-yl)ethanone | Combi-Blocks, Inc. | MFCD00548461 | 192.240 | C9H8N2OS | 95.000 | CC(=O)c1ccc2nc(N)sc2c1 | 1g | 603147161](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502192384.JPG-250.jpg)
eMolecules 21222-61-7 | 1-(2-Aminobenzo[d]thiazol-6-yl)ethanone | Combi-Blocks, Inc. | MFCD00548461 | 192.240 | C9H8N2OS | 95.000 | CC(=O)c1ccc2nc(N)sc2c1 | 1g | 603147161
1-(2-Aminobenzo[d]thiazol-6-yl)ethanone | Combi-Blocks, Inc. | 21222-61-7 | MFCD00548461 | 192.240 | C9H8N2OS | 95.000 | CC(=O)c1ccc2nc(N)sc2c1 | 1g | 603147161
Aobchem (2 6-Difluorophenyl)(thiophen-2-yl)methanol | 95% | CAS 1249018-33-4 | C11H8F2OS | 250mg
(2 6-Difluorophenyl)(thiophen-2-yl)methanol | 95% | CAS 1249018-33-4 | C11H8F2OS | 250mg
Aobchem 2-Chloro-4-fluoro-3-(methylthio)pyridine | 97% | CAS 1935995-08-6 | C6H5ClFNS | 1g
2-Chloro-4-fluoro-3-(methylthio)pyridine | 97% | CAS 1935995-08-6 | C6H5ClFNS | 1g
Medchemexpress LLC PF-670462 dihydrochloride | 950912-80-8 | C19H22Cl2FN5 | 5 MG
PF-670462 dihydrochloride is a potent and selective inhibitor of casein kinase (CK1ε and CK1δ) and a potent inhibitor of Wnt/β-catenin signaling. In vivo, it produces robust phase delays in circadian rhythms, affecting gene transcription in the liver, pancreas, and suprachiasmatic nucleus.
- Potent and selective inhibitor of CKIε and CKIδ
- Potent inhibitor of Wnt/β-catenin signaling
- Lower selectivity for EGFR and SAPK2A/p38
- Causes GFP signal redistribution to the cytoplasm
- Produces robust phase delays in circadian rhythms in rats
- Delays rhythmic transcription of Bmal1, Per1, Per2, and Nr1d1 in liver and pancreas
- Delays Nr1d1 and Dbp mRNA expression in the suprachiasmatic nucleus
Medchemexpress LLC Methyl 3-aminopyridine-4-carboxylate | 55279-30-6 | 152.15 | 10 G
Methyl 3-aminopyridine-4-carboxylate is a biochemical reagent suitable for life science-related research. This compound is provided as an off-white to yellow solid.
- Biochemical reagent for research
- Suitable for biological material or organic compound studies
- Appears as an off-white to yellow solid
- Requires protection from light during storage
Medchemexpress LLC 2-Chloro-5-thiophenecarboxaldehyde | 7283-96-7 | 146.59 | 10 G
2-Chloro-5-thiophenecarboxaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
- Biochemical reagent
- Used as a biological material or organic compound for life science related research
Medchemexpress LLC Lesopitron dihydrochloride | 132449-89-9 | 98.0% | 393.74 g/mol | C15H23Cl3N6 | 5 MG
Lesopitron dihydrochloride is a selective, full agonist of the 5-HT1A receptor used in research to investigate serotonergic signaling and pharmacology. Supplier-reported data indicate activity in rodent tissues (IC50 ≈125 nM) and effects on adenylate cyclase activity and neuronal firing, supporting use in both in vitro and in vivo studies.
- Selective full 5-HT1A receptor agonist.
- Reported IC50 ≈125 nM in rat hippocampal membranes.
- Modulates forskolin-stimulated adenylate cyclase activity.
- Demonstrated activity in vitro and in vivo assays.
- Supplied in small, research-oriented pack sizes for pharmacology studies.
Medchemexpress LLC Way-100135 dihydrochloride | 149055-79-8 | 98.1% | 468.46 g/mol | C24H35Cl2N3O2 | 5 MG
WAY-100135 dihydrochloride is a research-grade small molecule used as a selective antagonist at presynaptic and postsynaptic 5-HT1A receptors. Supplied as the dihydrochloride salt with reported in vitro potency (IC50 ≈ 34 nM) and high purity, it is intended for pharmacology and neuroscience studies.
- Selective antagonist of 5-HT1A receptors.
- High purity suitable for analytical and preclinical research.
- Commonly used for receptor pharmacology and signaling studies.
- Available in small pack sizes for laboratory experiments.
- Molecular weight provided for dosing and calculation purposes.
Medchemexpress LLC Thiophene-2-amidoxim 500mg | 108443-93-2 | 142.18 g/mol | C5H6N2OS | 500 MG
Thiophene-2-amidoxime is a small-molecule synthetic intermediate used in pharmaceutical and medicinal chemistry as a precursor for constructing heterocyclic compounds and for method development in drug synthesis. It is supplied as a solid at research-grade purity for laboratory use.
- High purity suitable for research and synthesis applications.
- Solid form, easy to weigh and handle in standard laboratory procedures.
- Commonly used as a building block in heterocyclic and medicinal chemistry.
- Available in small lab-scale quantities for method development.
- Compatible with common organic solvents and standard synthetic reactions.
eMolecules 36052-27-4 | Methyl 3-aminopicolinate | ChemScene | MFCD08695602 | 152.153 | C7H8N2O2 | 97.000 | COC(=O)c1ncccc1N | 10g | 536904939
Methyl 3-aminopicolinate | ChemScene | 36052-27-4 | MFCD08695602 | 152.153 | C7H8N2O2 | 97.000 | COC(=O)c1ncccc1N | 10g | 536904939
Medchemexpress LLC Gyki 52466 dihydrochloride | 2319722-40-0 | MFCD00153803 | 99.8% | 366.24 g/mol | C17H17Cl2N3O2 | 10 MG
GYKI 52466 dihydrochloride is a selective, noncompetitive antagonist of AMPA and kainate ionotropic glutamate receptors used in pharmacological research into anticonvulsant effects, neuroprotection, and excitatory neurotransmission studies.
- Selective noncompetitive AMPA/kainate receptor antagonist.
- Orally active with documented anticonvulsant activity.
- High purity for research use (≈99.8%).
- Supplied in small-molecule research quantities (e.g., 10 MG).
- Molecular weight 366.24 g/mol; CAS 2319722-40-0.
- Store sealed, away from moisture and light; recommended storage at 4°C (in solvent: -80°C/-20°C for long-term/short-term).