Benzenesulfonamides
![eMolecules Medchem Express / FASN-IN-1 / 5mg / 455326028 / HY-111777 / / 1808260-84-5 / [null] / 395.540 / C18H25N3O3S2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502468017.JPG-250.jpg)
eMolecules Medchem Express / FASN-IN-1 / 5mg / 455326028 / HY-111777 / / 1808260-84-5 / [null] / 395.540 / C18H25N3O3S2
Medchem Express / FASN-IN-1 / 5mg / 455326028 / HY-111777 / / 1808260-84-5 / [null] / 395.540 / C18H25N3O3S2
eMolecules N-Benzyl 3-boronobenzenesulfonamide | 690662-91-0 | 1G | Purity: 98%
Combi-Blocks | N-Benzyl 3-boronobenzenesulfonamide | 1G | 690662-91-0 | MFCD07783857
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FUJIFILM BIOSCIENCES INC P-BROMOBENZENESULFONAMIDE 5 G
*Orders for this supplier are non-cancellable/non-returnable once they are processed.* P-bromobenzenesulfonamide 5 G. 701-34-8 MFCD00051977
Apexbio Technology LLC Sildenafil mesylate 1308285-21-3 500mg
Sildenafil mesylate (CAS 1308285-21-3) is a potent and selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5) exhibiting an IC50 of 3 5 nM By inhibiting PDE5-mediated cGMP hydrolysis it enhances endogenous cGMP levels particularly within corpus cavernosum tissue In vitro sildenafil mesylate reversibly potentiates relaxation responses in precontracted corpus cavernosum strips following sodium nitroprusside exposure or electrical stimulation and increases intracellular cGMP in treated smooth muscle cells In vivo it augments erectile responses in anesthetized canine models This compound is widely used for studying PDE5-related signaling pathways and pharmacological modulation in erectile and vascular function research
![eMolecules Medchem Express / Rezivertinib analogue 1 / 5mg / 728132635 / HY-148053 / / 2227103-37-7 / [null] / 487.608 / C27H33N7O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502455808.PNG-250.jpg)
eMolecules Medchem Express / Rezivertinib analogue 1 / 5mg / 728132635 / HY-148053 / / 2227103-37-7 / [null] / 487.608 / C27H33N7O2
Medchem Express / Rezivertinib analogue 1 / 5mg / 728132635 / HY-148053 / / 2227103-37-7 / [null] / 487.608 / C27H33N7O2
Medchemexpress LLC Oregon green 488 azide | 2648246-11-9 | 98.0% | 637.67 | C33H37F2N5O6 | 10 MG
Oregon Green 488 azide is a green-fluorescent azide reagent used to label alkyne-modified biomolecules via copper-catalyzed azide-alkyne cycloaddition (click chemistry). It is supplied as a solid dye with high purity for biochemical assays and fluorescence labeling.
- Bright green-fluorescent azide probe for click chemistry.
- Reacts selectively with terminal alkynes via copper-catalyzed azide-alkyne cycloaddition.
- High purity (98.0%) suitable for biochemical assays.
- Solid, orange to red appearance for easy handling and storage.
- Storage: sealed, away from moisture and light; in solvent: -80°C (6 months), -20°C (1 month).
- Available in multiple pack sizes, including 10 MG.
![Medchemexpress LLC 4-[[(hexylamino)carbonyl]amino]-N-[4-[2-[[(2S)-2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethyl]-phe | 159182-43-1 | 98.9% | 584.73 g/mol | C30H40N4O6S | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000298390.png-250.jpg)
Medchemexpress LLC 4-[[(hexylamino)carbonyl]amino]-N-[4-[2-[[(2S)-2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethyl]-phe | 159182-43-1 | 98.9% | 584.73 g/mol | C30H40N4O6S | 10 MG
This compound is a potent, selective β3-adrenergic receptor agonist (IC50 35 nM) reported to enhance homology-directed repair (HDR)-mediated genome editing. It is supplied as a high-purity solid with characterized molecular and storage properties suitable for pharmacology and genome-editing research.
- Potent β3-adrenergic receptor agonist with IC50 of 35 nM.
- Enhances homology-directed repair (HDR) for genome-editing applications.
- High purity suitable for research use.
- Solid, white to off-white appearance for easy handling.
- Stable storage profile for powder and for solutions.