Benzenesulfonamides
![eMolecules 23672-07-3 | N-{[(2S)-1-Ethylpyrrolidin-2-yl]methyl}-2-methoxy-5-sulfamoylbenzamide | Combi-Blocks | MFCD00055220 | 341.430 | C15H23N3O4S | 98.000 | CCN1CCC[C@H]1CNC(=O)c1cc(ccc1OC)S(N)(=O)=O | 25g | 205398828](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502184054.JPG-250.jpg)
eMolecules 23672-07-3 | N-{[(2S)-1-Ethylpyrrolidin-2-yl]methyl}-2-methoxy-5-sulfamoylbenzamide | Combi-Blocks | MFCD00055220 | 341.430 | C15H23N3O4S | 98.000 | CCN1CCC[C@H]1CNC(=O)c1cc(ccc1OC)S(N)(=O)=O | 25g | 205398828
N-{[(2S)-1-Ethylpyrrolidin-2-yl]methyl}-2-methoxy-5-sulfamoylbenzamide | Combi-Blocks | 23672-07-3 | MFCD00055220 | 341.430 | C15H23N3O4S | 98.000 | CCN1CCC[C@H]1CNC(=O)c1cc(ccc1OC)S(N)(=O)=O | 25g | 205398828
Medchemexpress LLC HY-15465 5mg Medchemexpress, KN-93 CAS:139298-40-1 Purity:>98%
Medchemexpress, HY-15465 5mg KN-93 CAS:139298-40-1 KN-93 is a cell-permeable, reversible and competitive inhibitor calmodulin-dependent kinase type II (CaMKII) with a Ki of 370 nM. 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-A0013A 500mg Medchemexpress, Bosentan (hydrate) CAS:157212-55-0 Purity:>98%
Medchemexpress, HY-A0013A 500mg Bosentan (hydrate) CAS:157212-55-0 Bosentan hydrate is a competitive and dual antagonist of endothelin-1 (ET) for the ETA and ETB receptors with Ki of 4.7 nM and 95 nM in human SMC, respectively. 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.
Cayman Chemical Ndesmethyl Sildenafil citrat
A major metabolite of sildenafil; formed via oxidative metabolism of sildenafil by CYP3A4, CYP3A5, and CYP3A7
eMolecules 1808260-84-5 | Medchem Express | FASN-IN-1 | 5mg | 455326028 | HY-111777 | 395.54 | C18H25N3O3S2
Ambeed | (4S4S)-22-(13-Bis(4-(adamantan-1-yl)phenyl)propane-22-diyl)bis(4-benzyl-45-dihydrooxazole) | 250mg | 696731484 | A1501027 | 2757085-43-9 | 783.113 | C55H62N2O2
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Selleck Chemical LLC Sildenafil Mesylate S4683-500mg
Sildenafil Mesylate(UK-92480 Mesylate) is a mesylate form of Sildenafil an inhibitor of Phosphodiesterase 5
Medchemexpress LLC Rac-osmi-1 | 2748153-92-4 | 96.5% | 50 MG
Rac-OSMI-1 is the racemate of OSMI-1, a cell-permeable small-molecule inhibitor of O-GlcNAc transferase (OGT) used in cellular research to reduce protein O-linked N-acetylglucosamine (O-GlcNAc) modification.
- Inhibits O-GlcNAc transferase with reported IC50 ≈ 2.7 μM.
- Racemic small molecule for cellular research.
- Molecular weight 563.64 g/mol.
- Reported purity 96.5%.
- Available as a solid in a 50 mg package.
![Medchemexpress LLC 4-[[4-(2-butynyloxy)phenyl]sulfonyl]-N-hydroxy-2,2-dimethyl-(3S)thiomorpholinecarboxamide | 287403-39-8 | 99.6% | 398.50 g/mol | C17H22N2O5S2 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000248736.png-250.jpg)
Medchemexpress LLC 4-[[4-(2-butynyloxy)phenyl]sulfonyl]-N-hydroxy-2,2-dimethyl-(3S)thiomorpholinecarboxamide | 287403-39-8 | 99.6% | 398.50 g/mol | C17H22N2O5S2 | 100 MG
TMI-1 (WAY-171318) is a small-molecule inhibitor of TNF-α converting enzyme (TACE) with reported activity against ADAM-17, ADAMTS-4, and multiple MMPs. Supplied for research use, it has demonstrated oral activity and induces apoptosis in cancer cell models, and is provided with analytical documentation for laboratory studies.
- Purity 99.57%.
- Molecular formula C17H22N2O5S2.
- Molecular weight 398.50 g/mol.
- Available as solid (5 mg, 10 mg, 25 mg, 50 mg, 100 mg) and solution (10 mM in DMSO).
- Includes datasheet, COA, and SDS documentation.
- Suitable for biochemical, cell-based, and in vivo oral dosing research (research use only).
Medchemexpress LLC Sultiame | 61-56-3 | 98.9% | 290.36 g/mol | C10H14N2O4S2 | 100 MG
Sultiame is a carbonic anhydrase inhibitor widely used as an antiepileptic agent. This product is provided as research-grade analytical material intended for laboratory studies, assay calibration, and pharmacology investigations.
- Provides carbonic anhydrase inhibition for mechanism-of-action studies.
- Used as an antiepileptic agent in pharmacology and toxicology research.
- Analytical standard suitable for assay, calibration, and reference use.
- High purity, approximately 98.9%.
- Molecular weight 290.36 g/mol; formula C10H14N2O4S2.
- CAS number 61-56-3 for unambiguous identification.
- Available as solid and as a 10 mM DMSO solution for ready-to-use preparations.
- Multiple pack sizes available, including 100 MG solid.
Medchemexpress LLC Fedratinib hydrochloride hydrate | 1374744-69-0 | MFCD28137677 | 99.9% | 615.62 g·mol⁻¹ | C27H40Cl2N6O4S | 200 MG
Fedratinib (hydrochloride hydrate) is a potent, selective, ATP-competitive JAK2 inhibitor supplied as a solid for research into myeloproliferative disorders and cancer biology. The compound is well characterized chemically, with a defined formula and molecular weight suitable for biochemical and cellular studies.
- Potent, selective JAK2 inhibitor with low-nanomolar potency.
- High purity (>99.9%) confirmed by certificate of analysis.
- Molecular weight 615.62 g·mol⁻¹ and formula C27H40Cl2N6O4S.
- Supplied as a white to yellow solid, suitable for handling and storage.
- Available in multiple pack sizes, including a 200 MG unit.
- Suitable for in vitro and in vivo research applications.