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Filtered Search Results
Accela Chembio Inc 4-(difluoromethoxy)aniline | 100g | 22236-10-8 | MFCD00085005 | 98% | D: 1.283 | Shelf Life: 1080 Days | Light Sensitive/n2/+4
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4-(difluoromethoxy)aniline | 100g | 22236-10-8 | MFCD00085005 | 98% | D: 1.283 | Shelf Life: 1080 Days | Light Sensitive/n2/+4
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Medchemexpress LLC N-((1R,3S)-3-(4-acetylpiperazin-1-yl)cyclohexyl)-7-fluoro-4-methyl-1H-indole-2-carboxamide | 2411748-50-8 | 99.1% | C22H29FN4O2 | 10MG
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EZM0414 is a selective, orally bioavailable small-molecule inhibitor of the histone methyltransferase SETD2, developed for preclinical research applications. It exhibits potent biochemical and cellular activity and is intended for laboratory research into SETD2-driven biology and oncology models.
- Selective SETD2 inhibitor with biochemical IC50 ~18 nM.
- Demonstrates cellular activity (IC50 ~34 nM).
- Orally bioavailable in preclinical models.
- High purity (≈99%) suitable for biochemical and cellular assays.
- Applicable to research on hematologic and solid tumor models.
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Medchemexpress LLC Emvododstat (PTC299) | 1256565-36-2 | 99.9% | 467.34 g/mol | C25H20Cl2N2O3 | 50MG
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PTC299 (emvododstat) is an orally active small-molecule inhibitor that selectively suppresses VEGFA mRNA translation and inhibits dihydroorotate dehydrogenase (DHODH). Provided for research use, it is supplied as solid samples and DMSO solutions and is used in studies of VEGF regulation, pyrimidine biosynthesis, and oncology and immunology research.
- High purity: 99.9% by assay.
- Molecular weight: 467.34 g/mol.
- Chemical formula: C25H20Cl2N2O3.
- Physical appearance: white to light yellow solid.
- Available as solid and as 10 mM solution in DMSO.
- Suitable for studies of VEGF regulation and DHODH-related pathways.
- Offered in multiple package sizes including 50 mg.
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![eMolecules 58879-34-8 | (S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502148824.JPG-250.jpg)
eMolecules 58879-34-8 | (S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944
(S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | 58879-34-8 | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944
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Medchemexpress LLC SRC INHIBITOR 1 5MG
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Src Inhibitor 1 is a potent, ATP-competitive and selective dual site Src tyrosine kinase inhibitor with IC50 values of 44 nM for Src and 88nM for Lck.CAS No. : 179248-59-0
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Medchemexpress LLC Gallopamil hydrochloride | 16662-46-7 | MFCD00867067 | 99.2% | C28H41ClN2O5 | 10MG
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Gallopamil hydrochloride is the hydrochloride salt of gallopamil, a methoxy derivative of verapamil and an L-type calcium channel blocker. It is supplied as a white to off-white solid and as a ready-to-use DMSO solution for in vitro research into calcium channel function and cardiovascular pharmacology.
- Potent L-type calcium channel blocker for pharmacology studies.
- Available as solid and 10 mM solution in DMSO for convenient dosing.
- High purity suitable for biochemical and cellular assays.
- Characterized by verified CAS, formula, and molecular weight for reproducibility.
- Provided with datasheet and certificate of analysis for traceability.
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Medchemexpress LLC Propoxycaine hydrochloride | 550-83-4 | MFCD01660627 | 99.7% | 330.85 | C16H27ClN2O3 | 10 MG
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Propoxycaine hydrochloride is an ester-type local anesthetic and sodium-channel inhibitor supplied as a solid research reagent. It is used in laboratory studies requiring blockade of voltage-gated sodium channels and is provided with documentation for purity and storage.
- Inhibits voltage-gated sodium channels, reducing nerve impulse conduction.
- Supplied as a white to light brown solid suitable for in vitro use.
- Molecular formula C16H27ClN2O3 and molecular weight 330.85 g/mol.
- High purity (≈99.7-99.98%) with available certificate of analysis.
- Storage recommendations: 4°C sealed for solid; in solvent -80°C (6 months) or -20°C (1 month).
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![Medchemexpress LLC 3-piperidinecarboxamide, 1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl) | 1207113-88-9 | 99.3% | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000232128.png-250.jpg)
Medchemexpress LLC 3-piperidinecarboxamide, 1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl) | 1207113-88-9 | 99.3% | 100 MG
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CCG-100602 is a small-molecule inhibitor that selectively blocks myocardin-related transcription factor A (MRTF-A) / serum response factor (SRF) signaling by preventing MRTF-A nuclear localization; supplied as a white to off-white solid for research use.
- Selective MRTF-A/SRF pathway inhibitor.
- CAS 1207113-88-9.
- Molecular weight 478.82 g/mol.
- Purity 99.29% (LCMS).
- Available as solid (5-500 mg) and as 10 mM DMSO solutions.
- Store solid at 4°C; in solvent store at -80°C for long-term.
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Medchemexpress LLC Mps1-IN-3 hydrochloride | 2989453-29-2 | 98.0% | 574.09 | C26H32ClN7O4S | 100MG
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Mps1-IN-3 hydrochloride is a potent, selective inhibitor of the Mps1 (TTK) kinase with an IC50 of approximately 50 nM. It inhibits proliferation of glioblastoma cells and sensitizes glioblastoma xenografts to vincristine in preclinical models. The compound is supplied as the hydrochloride salt in solid form for research use.
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eMolecules 2682097-49-8 | (S)-(1-Methylazetidin-2-yl)methanamine dihydrochloride | 100mg
Pharmablock | 4-chloro-8-methoxy-2-methylquinoline | 25mg | 794216359 | PB96024 | 64951-58-2 | MFCD00272401 | 207.660 | C11H10ClNO
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Selleck Chemical LLC AST-487
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AST-487 (NVP-AST487) a N N -diphenyl urea is an ATP competitive inhibitor of Flt3 with ki of 0 12 M Besides FLT3 AST487 also inhibits RET KDR c-KIT and c-ABL kinase with IC50 values below 1 M
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Medchemexpress LLC N-[4-[(E)-2-[3-t-Bu-5-(2,4-dioxopyrimidin-1-yl)-2-methoxyphenyl]ethenyl]phenyl]methanesulfonamide | 1132936-00-5 | MFCD28502074 | 99.8% | 469.6 g/mol | C24H27N3O5S | 50 MG
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ABT-072 is an orally active, non-nucleoside inhibitor of the hepatitis C virus NS5B polymerase used as a research compound. It demonstrates sub-nanomolar to low-nanomolar antiviral activity against genotype 1 polymerases and is supplied for in vitro and preclinical investigations.
- Potent NS5B inhibition (GT1a EC50 = 1 nM; GT1b EC50 = 0.3 nM).
- Orally bioavailable profile observed in preclinical studies.
- High purity suitable for research use.
- Well-characterized chemical identity (CAS 1132936-00-5).
- Suitable as a reference compound in antiviral assays.
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eMolecules 677772-84-8 | Medchem Express | MRK-560 | 5mg | 482204368 | HY-14174 | MFCD09970622 | 517.91 | C19H17ClF5NO4S2
Medchem Express | MRK-560 | 5mg | 482204368 | HY-14174 | 677772-84-8 | MFCD09970622 | 517.910 | C19H17ClF5NO4S2
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eMolecules 103860-60-2 | 2,3-Dihydroxynaphthalene-1,4-dicarbaldehyde | MFCD09800457 | 100mg
Medchem Express | Terevalefim | 5mg | 665626281 | HY-137455 | 1070881-42-3 | 176.240 | C9H8N2S
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Medchemexpress LLC Propoxycaine hydrochloride | 550-83-4 | 99.7% | 100 MG
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Propoxycaine hydrochloride inhibits voltage-gated sodium channels, and thereby inhibits the ionic flux required for the initiation and conduction of impulses. Propoxycaine hydrochloride application can lead to a loss of sensation.
- Sodium channel inhibitor
- Inhibits voltage-gated sodium channels
- Inhibits the ionic flux required for the initiation and conduction of impulses
- Can lead to a loss of sensation
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