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Filtered Search Results
Matrix Scientific 2-CHLORO-6-FLUOROPHENYLACET-5G
2-Chloro-6-fluorophenylacetic acid, 98%-5g,C8H6ClFO2, MFCD00004319, mw 188.59,
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Medchemexpress LLC Retagliptin | 1174122-54-3 | 98.5% | 464.36 | C19H18F6N4O3 | 5 MG
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Retagliptin (SP2086) is a selective, competitive, and orally active dipeptidyl peptidase-4 (DPP-4) inhibitor used in preclinical research on type 2 diabetes mellitus (T2DM). By inhibiting DPP-4, it prevents GLP-1 degradation and amplifies incretin signaling to improve glycemic responses in research models. The compound is supplied as a solid with high purity suitable for biochemical and cellular assays.
- Selective, competitive DPP-4 inhibition for targeted mechanistic studies.
- Orally active compound class commonly used in T2DM research models.
- Inhibits GLP-1 degradation to amplify incretin-mediated insulin release.
- High purity (98.5%) suitable for biochemical and cellular assays.
- Solid form with defined molecular formula and molecular weight for analytical work.
- Provided in small research-scale packaging for screening and validation studies.
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Medchemexpress LLC Temafloxacin | 108319-06-8 | 99.65% | 417.38 | 5 MG
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Temafloxacin (TMFX) is an orally active quinolone broad-spectrum antibacterial agent. It is well tolerated in lower respiratory and genitourinary tract infections, demonstrating good antibacterial activity against gram-positive and gram-negative bacteria, with specific MIC ranges for E. coli, P. aeruginosa, and S. aureus. It shows good inhibitory activity in murine pyelonephritis and, as the hydrochloride form, rapid gastrointestinal absorption with excellent tissue and body fluid penetration.
- Orally active quinolone broad-spectrum antibacterial agent
- Well tolerated in lower respiratory and genitourinary tract infections
- Exhibits good antibacterial activity against gram-positive and gram-negative bacteria
- Demonstrates good inhibitory activity against murine pyelonephritis
- Rapid gastrointestinal absorption and excellent tissue and body fluid penetration
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Medchemexpress LLC JNJ 303 | 878489-28-2 | 98.7% | 440.98 | 5 MG
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JNJ-303 is a specific delayed rectifier Kv blocker that can potently inhibit IKs with an IC50 value of 64 nM. It is indicated for research related to diabetes, obesity, and the central nervous system.
- Specific delayed rectifier Kv blocker.
- Potently blocks IKs with an IC50 value of 64 nM.
- Can be utilized for research on diabetes, obesity, and the central nervous system.
- At a concentration of 3.3 μM, JNJ 303 shows no effects on other cardiac channels.
- It has been observed to induce QT-prolongations and unprovoked torsades de pointes (TdP).
- In mice, JNJ 303 recapitulates the Exn4-induced reduction in fasting blood glucose levels.
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eMolecules 936500-94-6 | Medchem Express | Elinogrel | 5mg | 475641490 | HY-11021 | MFCD16619373 | 523.94 | C20H15ClFN5O5S2
Medchem Express | Elinogrel | 5mg | 475641490 | HY-11021 | 936500-94-6 | MFCD16619373 | 523.940 | C20H15ClFN5O5S2
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eMolecules 350682-84-7 | 4-BIPHENYL-3',5'-DIFLUORO-CARBOXYLIC ACID | AstaTech | MFCD03839971 | 234.202 | C13H8F2O2 | 97.000 | OC(=O)c1ccc(cc1)-c1cc(F)cc(F)c1 | 0.25g | 112530510
4-BIPHENYL-3',5'-DIFLUORO-CARBOXYLIC ACID | AstaTech | 350682-84-7 | MFCD03839971 | 234.202 | C13H8F2O2 | 97.000 | OC(=O)c1ccc(cc1)-c1cc(F)cc(F)c1 | 0.25g | 112530510
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![Medchemexpress LLC 3-[4-[(dimethylamino)methyl]phenyl]-N-methyl-N-[5-[3-methyl-5-(1,3,5-trimethyl-1H-pyrazol-4-yl)-2-pyri... | 2830555-70-7 | 98.0% | C32H35N9O | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000259778.png-250.jpg)
Medchemexpress LLC 3-[4-[(dimethylamino)methyl]phenyl]-N-methyl-N-[5-[3-methyl-5-(1,3,5-trimethyl-1H-pyrazol-4-yl)-2-pyri... | 2830555-70-7 | 98.0% | C32H35N9O | 10MG
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AZ14145845 is a selective type I1/2 dual Mer and Axl kinase inhibitor developed for research use with demonstrated in vivo efficacy. It is supplied as a white to off-white solid, has molecular formula C32H35N9O and molecular weight 561.68, and is provided at high purity for preclinical and laboratory applications.
- Selective inhibition of Mer and Axl kinases.
- Demonstrated in vivo efficacy in preclinical models.
- High chemical purity suitable for biochemical and cellular assays.
- Available in small-scale quantities and solution formulations for screening.
- White to off-white solid with standard laboratory storage characteristics.
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Medchemexpress LLC Rac-lunresertib | 2719749-28-5 | MFCD34645920 | 99.7% | 324.38 | C18H20N4O2 | 5 MG
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(Rac)-lunresertib is a racemic, small-molecule inhibitor of the membrane-associated tyrosine- and threonine-specific kinase Myt1 (PKMYT1). It is used as a research reagent in preclinical studies of cell-cycle regulation and anticancer activity and is supplied as a solid or solution with high reported purity. Molecular formula C18H20N4O2; molecular weight 324.38 g/mol.
- Potent Myt1 inhibition with reported IC50 <10 nM.
- Suitable for in vitro and preclinical cell-cycle and oncology research.
- High reported purity (99.72%).
- Available as an off-white to yellow solid and as solution formulations.
- Racemic small molecule, convenient handling and storage for lab use.
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Accela Chembio Inc 3-amino-4-fluorobenzonitrile | 5g | 859855-53-1 | MFCD07787428 | 97+% | Shelf Life: 1440 Days | Light Sensitive/n2
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3-amino-4-fluorobenzonitrile | 5g | 859855-53-1 | MFCD07787428 | 97+% | Shelf Life: 1440 Days | Light Sensitive/n2
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Chemscene ChemScene | 2,6-Dichloro-4-fluoroaniline | 10G | CS-W017244 | 0.98 | 344-19-4| MFCD00142845 | 180.009
ChemScene | 2,6-Dichloro-4-fluoroaniline | 10G | CS-W017244 | 0.98 | 344-19-4| MFCD00142845 | 180.009
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Medchemexpress LLC Azd-4818 | 1003566-93-5 | 99.1% | 567.46 g/mol | C27H32Cl2N2O7 | 10 MG
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AZD-4818 is a potent, orally active antagonist of the chemokine receptor CCR1 used in respiratory inflammation research. It blocks CCR1-mediated recruitment of inflammatory cells and has been evaluated in preclinical models and clinical tolerability studies for chronic obstructive pulmonary disease. Supplied as a solid with documented solubility and storage instructions for laboratory use.
- Potent CCR1 antagonism, reducing monocyte and neutrophil recruitment.
- Orally bioavailable profile suitable for dosing studies.
- High chemical purity for reliable experimental results.
- Provided with solubility and storage data for reproducible handling.
- Multiple pack sizes available for flexible experimental needs.
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eMolecules 1233958-47-8 | ChemScene | 2-Ethoxy-3-fluoroaniline | 100mg | 714232371 | CS-0299307 | MFCD17014144 | 155.172 | C8H10FNO
Ambeed | 2-Fluoro-5-(methylsulfonamido)benzoic acid | 250mg | 682931880 | A790325 | 137315-01-6 | MFCD12149130 | 233.210 | C8H8FNO4S
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BLD PHARMATECH CO LIMITED 3-(4-Fluorophenyl)propanenitrile,25468-86-4
3-(4-Fluorophenyl)propanenitrile,25468-86-4
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Apexbio Technology LLC Penfluridol 26864-56-2 50mg
Penfluridol (CAS 26864-56-2) is a first-generation antipsychotic belonging to the diphenylbutylpiperidine class It acts primarily as a dopamine D2 receptor antagonist disrupting dopaminergic neurotransmission in the central nervous system Penfluridol has been widely used in research to investigate dopaminergic signaling pathways and the pharmacology of antipsychotic agents Its molecular profile supports studies of receptor binding antipsychotic efficacy and the neurobiological basis of schizophrenia and related disorders
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eMolecules 125995-03-1 | Medchem Express | Atorvastatin lactone | 5mg | 687442457 | HY-101873 | MFCD00899262 | 540.635 | C33H33FN2O4
Ambeed | 25-Dioxopyrrolidin-1-yl 3-(2-(2-(prop-2-yn-1-yloxy)ethoxy)ethoxy)propanoate | 250mg | 642080527 | A310681 | 1428629-71-3 | MFCD23726610 | 313.306 | C14H19NO7
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