Benzenesulfonamides
Accela Chembio Inc N-fluorobenzenesulfonimide | 100g | 133745-75-2 | MFCD00144885 | 97% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive
N-fluorobenzenesulfonimide | 100g | 133745-75-2 | MFCD00144885 | 97% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive
Medchemexpress LLC HY-15383 5mg Medchemexpress, Glyparamide CAS:5581-42-0 Purity:>98%
Medchemexpress, HY-15383 5mg Glyparamide CAS:5581-42-0 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.
eMolecules 133745-75-2 | N-Fluorobenzenesulfonimide | Ambeed | MFCD00144885 | 315.330 | C12H10FNO4S2 | 98.000 | FN(S(=O)(=O)c1ccccc1)S(=O)(=O)c1ccccc1 | 10g | 490562797
N-Fluorobenzenesulfonimide | Ambeed | 133745-75-2 | MFCD00144885 | 315.330 | C12H10FNO4S2 | 98.000 | FN(S(=O)(=O)c1ccccc1)S(=O)(=O)c1ccccc1 | 10g | 490562797
Apexbio Technology LLC SUCCINYLSULFATHIAZOLE-200MG
Succinylsulfathiazole (CAS No 116-43-8) is an antibacterial agent primarily used in biomedical research focused on gastrointestinal infections Originating from the sulfonamide class of compounds it works by inhibiting the bacterial folic acid synthesis pathway hindering the growth and proliferation of pathogens Its in vitro activity is typically observed in the micromolar range making it effective in controlled environments Succinylsulfathiazole is commonly utilized in cell-based assays and animal models to study enteric bacterial infections and the efficacy of similar antimicrobial agents It plays a significant role in drug screening processes where its impact on various bacterial strains in the gastrointestinal tract is evaluated Experimental concentrations typically depend on the specific research design This compound remains an important tool for researchers exploring new ways to combat bacterial infections particularly those resistant to traditional antibiotics
Medchemexpress LLC IACS-13909 | 2160546-07-4 | 99.97% | 377.27 | 25 MG
IACS-13909 is a selective, potent, and orally active SHP2 allosteric inhibitor with an IC50 of 15.7 nM and a Kd of 32 nM. It demonstrates greater selectivity for SHP2 compared to other phosphatases, including SHP1. This compound exhibits antitumor activities and effectively suppresses MAPK pathway signaling in receptor tyrosine kinase (RTK)-dependent cancers.
- Selective, potent, and orally active SHP2 allosteric inhibitor
- Greater selectivity for SHP2 compared to other phosphatases
- Exhibits antitumor activities
- Suppresses MAPK pathway signaling in RTK-dependent cancers
Selleck Chemical LLC Sildenafil Citrate S1431-1g
Sildenafil Citrate a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5) is a well-tolerated and highly effective treatment for erectile dysfunction
eMolecules 1100095-14-4 | 4-Methoxy-3-(N-morpholinylsulfonyl)phenylboronic acid | Combi-Blocks | MFCD08056366 | 301.120 | C11H16BNO6S | 98.000 | COc1ccc(cc1S(=O)(=O)N1CCOCC1)B(O)O | 5g | 117522193
4-Methoxy-3-(N-morpholinylsulfonyl)phenylboronic acid | Combi-Blocks | 1100095-14-4 | MFCD08056366 | 301.120 | C11H16BNO6S | 98.000 | COc1ccc(cc1S(=O)(=O)N1CCOCC1)B(O)O | 5g | 117522193
Apexbio Technology LLC Sildenafil 139755-83-2 1mL(10 mM in DMSO)
Sildenafil (CAS 139755-83-2) is a small molecule inhibitor of phosphodiesterase type 5 (PDE5) By selectively blocking PDE5 activity sildenafil increases intracellular levels of cyclic guanosine monophosphate (cGMP) thereby modulating smooth muscle relaxation The compound exhibits an IC50 value of 5 22 nM against PDE5 indicating high potency in enzymatic assays Sildenafil is widely utilized in biomedical research to study cGMP signaling pathways and vascular smooth muscle physiology as well as to evaluate mechanisms underlying vasodilation and related pathophysiological conditions
Medchemexpress LLC HY-10341 500mg , Fasudil (Hydrochloride) HA-1077;AT-877;Fasudil HCl CAS:105628-07-7 Purity:98%
Medchemexpress, HY-10341 500mg Fasudil (Hydrochloride) HA-1077;AT-877;Fasudil HCl CAS:105628-07-7 Formula:C14H18ClN3O2S Ki: 0.33 μM (ROCK1), 1.0 μM (PKA), 9.3 μM (PKC), 55 μM (MLCK) [8] Purity:98% Fasudil Hydrochloride is a potent inhibitor of ROCK1 , PKA , PKC , and MLCK with K i of 0.33 μM, 1.0 μM, 9.3 μM and 55 μM, respectively. 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.