Benzenesulfonamides
eMolecules 608512-97-6 | Medchem Express | PKR-IN-C16 | 5mg | 705860907 | HY-13977A | MFCD28135662 | 268.29 | C13H8N4OS
Medchem Express | PKR-IN-C16 | 5mg | 705860907 | HY-13977A | 608512-97-6 | MFCD28135662 | 268.290 | C13H8N4OS
Selleck Chemical LLC Sulfasalazine S1576-1g
Sulfasalazine is a sulfa derivative of mesalazine used as an anti-inflammatory agent to treat bowel disease and rheumatoid arthritis Sulfasalazine is a potent and specific inhibitor of nuclear factor kappa B (NF- B) TGF- and COX-2 Sulfasalazine induces ferroptosis apoptosis and autophagy
Apexbio Technology LLC Glimepiride 93479-97-1 10mM (in 1mL DMSO)
Glimepiride (CAS 93479-97-1) is a sulfonylurea compound widely used in research on type 2 diabetes It primarily acts by enhancing glucose uptake both in the presence and absence of insulin In cultured cells glimepiride (10 M) increases 2-deoxyglucose uptake to 186% of control and upregulates GLUT1 and GLUT4 expression to 164% and 148% of control respectively indicating insulin-independent mechanisms for stimulating cardiac glucose uptake In rodent models glimepiride administration reduced diabetes incidence by 23% in BB rats and decreased blood glucose HbA1c and plasma insulin levels in KK-Ay mice highlighting its utility for investigating glucose metabolism and diabetes pathophysiology
Medchemexpress LLC HY-111383 5mg Medchemexpress, LX2343 CAS:333745-53-2 Purity:>98%
Medchemexpress, HY-111383 5mg LX2343 CAS:333745-53-2 LX2343 is a BACE1 enzyme inhibitor with an IC50 value of 11.43±0.36 μM. LX2343 acts as a non-ATP competitive PI3K inhibitor with an IC50 of 15.99±3.23 μM. LX2343 stimulates autophagy in its promotion of Aβ clearance. 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 871266-63-6 | PCI-27483 | MFCD25976837 | 0.1g
AstaTech | PCI-27483 | 0.1g | 551677127 | 40610 | 95.000 | 871266-63-6 | MFCD25976837 | 596.570 | C26H24N6O9S
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eMolecules 151720-43-3 | Medchem Express | Oxamflatin | 1mg | 446257610 | HY-102033 | MFCD00949087 | 342.37 | C17H14N2O4S
ChemScene | 1-Methyl-1H-indole-6-carbonitrile | 1g | 791178640 | CS-0043605 | 20996-87-6 | MFCD08690254 | 156.188 | C10H8N2
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Medchemexpress LLC Sildenafil (citrate) | 171599-83-0 | C28H38N6O11S | 5 G
Sildenafil citrate is a potent phosphodiesterase type 5 (PDE5) inhibitor with an IC50 of 5.22 nM. It is intended for research use only.
- Potent phosphodiesterase type 5 (PDE5) inhibitor with IC50 of 5.22 nM.
- Potentiates phosphorylation of ERK1/ERK2.
- Increases percentage of cells in S phase and cell proliferation.
- Enhances upregulation of ERK1/ERK2 phosphorylation induced by serotonin.
- Increases intracavernosal pressure (ICP) and ICP/BP in dog models.
- Reduces the number of TL+-cells and microglia/macrophages in ischemic models.
- Decreases flap necrosis by increasing growth factors (FGF and VEGF).
- Used in clinical trials for pulmonary arterial hypertension, erectile dysfunction, spinal cord injuries, pregnancy complication, cancer, and more.
Apexbio Technology LLC Glimepiride 93479-97-1 5g
Glimepiride (CAS 93479-97-1) is a sulfonylurea compound widely used in research on type 2 diabetes It primarily acts by enhancing glucose uptake both in the presence and absence of insulin In cultured cells glimepiride (10 M) increases 2-deoxyglucose uptake to 186% of control and upregulates GLUT1 and GLUT4 expression to 164% and 148% of control respectively indicating insulin-independent mechanisms for stimulating cardiac glucose uptake In rodent models glimepiride administration reduced diabetes incidence by 23% in BB rats and decreased blood glucose HbA1c and plasma insulin levels in KK-Ay mice highlighting its utility for investigating glucose metabolism and diabetes pathophysiology
Cayman Chemical Ndesmethyl Sildenafil citrat
A major metabolite of sildenafil; formed via oxidative metabolism of sildenafil by CYP3A4, CYP3A5, and CYP3A7
Medchemexpress LLC HY-100573 5mg Medchemexpress, (E)-Necrosulfonamide CAS:1360614-48-7 Purity:>98%
Medchemexpress, HY-100573 5mg (E)-Necrosulfonamide CAS:1360614-48-7 (E)-Necrosulfonamide is a necroptosis inhibitor acting by selectively targeting the mixed lineage kinase domain-like protein (MLKL) to block the necrosome formation. 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 1315323-00-2 | Medchem Express | Pyr10 | 5mg | 446269836 | HY-19408 | MFCD28411625 | 449.37 | C18H13F6N3O2S
Ambeed | 4-(ethoxymethylene)-2-phenyloxazol-5(4H)-one | 1g | 572842109 | A818543 | 15646-46-5 | 217.224 | C12H11NO3
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eMolecules 330161-87-0 | SU6656 | MFCD10565928 | 50mg
Ambeed | 3-(Furan-2-ylmethyl)-18-dimethyl-1H-purine-26(3H7H)-dione | 1mg | 598442356 | A389771 | 80288-49-9 | MFCD00153799 | 260.253 | C12H12N4O3
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eMolecules 402713-81-9 | Medchem Express | SB-399885 hydrochloride | 5mg | 446257985 | HY-103099 | MFCD09970355 | 482.8 | C18H22Cl3N3O4S
Medchem Express | BPU-11 | 5mg | 784543790 | HY-119102 | 909664-41-1 | 501.634 | C32H31N5O
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eMolecules 221290-14-8 | t-Butyl 3-boronobenzenesulfonamide | Combi-Blocks | MFCD06659842 | 257.110 | C10H16BNO4S | 98.000 | CC(C)(C)NS(=O)(=O)c1cccc(c1)B(O)O | 1g | 117521151
t-Butyl 3-boronobenzenesulfonamide | Combi-Blocks | 221290-14-8 | MFCD06659842 | 257.110 | C10H16BNO4S | 98.000 | CC(C)(C)NS(=O)(=O)c1cccc(c1)B(O)O | 1g | 117521151