Benzenesulfonamides
eMolecules 942206-85-1 | Medchem Express | GSK1016790A | 5mg | 446269983 | HY-19608 | MFCD12912413 | 655.61 | C28H32Cl2N4O6S2
Medchem Express | GSK1016790A | 5mg | 446269983 | HY-19608 | 942206-85-1 | MFCD12912413 | 655.610 | C28H32Cl2N4O6S2
Medchemexpress LLC HY-B0397 10mg Medchemexpress, Dichlorphenamide CAS:120-97-8 Purity:>98%
Medchemexpress, HY-B0397 10mg Dichlorphenamide CAS:120-97-8 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 17497-85-7 | 1,3,5-Tribromo-1,3,5-triazinane-2,4,6-trione | Accela ChemBio (ASD) | MFCD21604032 | 365.763 | C3Br3N3O3 | 95.000 | Brn1c(=O)n(Br)c(=O)n(Br)c1=O | 10g | 510410089
1,3,5-Tribromo-1,3,5-triazinane-2,4,6-trione | Accela ChemBio (ASD) | 17497-85-7 | MFCD21604032 | 365.763 | C3Br3N3O3 | 95.000 | Brn1c(=O)n(Br)c(=O)n(Br)c1=O | 10g | 510410089
Apexbio Technology LLC N-Desmethyl Sildenafil 139755-82-1 5mg
N-Desmethyl Sildenafil (CAS 139755-82-1) is a pharmacologically active metabolite of sildenafil It acts as a selective inhibitor of phosphodiesterase type 5 (PDE5) modulating intracellular signaling pathways by preventing the degradation of cyclic guanosine monophosphate (cGMP) Experimental studies have demonstrated its inhibitory activity toward PDE5 implicating a role in the modulation of vascular and smooth muscle functions N-Desmethyl Sildenafil is utilized in biomedical research to study PDE5-related cellular processes and to explore potential therapeutic strategies targeting this enzyme
Medchemexpress LLC Furosemide sodium | 41733-55-5 | MFCD23379919 | 99.9% | 500 MG
Furosemide sodium is a potent and orally active inhibitor of Na+/K+/2Cl- (NKCC) cotransporter, specifically NKCC1 and NKCC2. It also acts as a GABAA receptors antagonist, exhibiting 100-fold selectivity for α6-containing receptors over α1-containing receptors. This compound functions as a loop diuretic and is utilized in the study of congestive heart failure, hypertension, and edema. It is intended for research use only and is not sold to patients.
- Potent and orally active inhibitor of NKCC1 and NKCC2 cotransporters
- Functions as a GABAA receptors antagonist
- Exhibits 100-fold selectivity for α6-containing receptors over α1-containing receptors
- Acts as a loop diuretic
- Used in studies of congestive heart failure, hypertension, and edema
- Intended for research use only
Medchemexpress LLC Glimepiride impurity 1 | 119018-30-3 | MFCD08282469 | 25mg
Glimepiride impurity 1 is an impurity of Glimepiride (HY-B0104)
Medchemexpress LLC HY-15370A 10mg Medchemexpress, SB-269970 (hydrochloride) CAS:261901-57-9 Purity:>98%
Medchemexpress, HY-15370A 10mg SB-269970 (hydrochloride) CAS:261901-57-9 SB269970 hydrochloride (SB-269970A) is a hydrochloride salt form of SB-269970, which is a 5-HT7 receptor antagonist with the pKi of 8.3, exhibits >50-fold selectivity against other receptors. 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 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.
Sigma Aldrich Fine Chemicals Biosciences Glimepiride | 93479-97-1 | MFCD00878417 | 50 mg
Glimepiride | Purity: ≥98% | Mol Wt: 490.62 | 93479-97-1 | MFCD00878417 | 50 mg
Apexbio Technology LLC N-Desmethyl Sildenafil 139755-82-1 25mg
N-Desmethyl Sildenafil (CAS 139755-82-1) is a pharmacologically active metabolite of sildenafil It acts as a selective inhibitor of phosphodiesterase type 5 (PDE5) modulating intracellular signaling pathways by preventing the degradation of cyclic guanosine monophosphate (cGMP) Experimental studies have demonstrated its inhibitory activity toward PDE5 implicating a role in the modulation of vascular and smooth muscle functions N-Desmethyl Sildenafil is utilized in biomedical research to study PDE5-related cellular processes and to explore potential therapeutic strategies targeting this enzyme
Medchemexpress LLC Yap/taz inhibitor-2 | 2762617-31-0 | 99.8% | C19H14F4N4O | 10MG
YAP/TAZ inhibitor-2 is a small-molecule TEAD-YAP/TAZ inhibitor with potent nanomolar activity that disrupts TEAD-YAP/TAZ signaling, shows antiproliferative effects in cancer cell lines, and demonstrates oral activity in vivo. The compound is supplied as a light yellow solid with documented solubility, storage, and purity information.
- Potent TEAD-YAP/TAZ inhibition (EC50 = 3 nM).
- Antiproliferative activity in NCI-H226 cells (IC50 = 5.33 nM).
- High chemical purity (99.81%).
- Soluble in DMSO (100 mg/mL).
- Stable as powder at -20°C for long-term storage.
- Light yellow to yellow solid appearance.
Med Vet International Sildenafil, (Generic Viagra), 50mg, 100ct Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
RX SILDENAFIL, (GENERIC VIAGRA), 50MG, 100CT TABLETS
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
Aobchem N N-diethylthiophene-2-sulfonamide | 95% | CAS 41895-11-8 | C8H13NO2S2 | 5g
N N-diethylthiophene-2-sulfonamide | 95% | CAS 41895-11-8 | C8H13NO2S2 | 5g
Aobchem Benzenesulfonamide 3-methoxy-N N 4-trimethyl- | 95% | CAS 3101349-66-7 | C10H15NO3S | 1g
Benzenesulfonamide 3-methoxy-N N 4-trimethyl- | 95% | CAS 3101349-66-7 | C10H15NO3S | 1g