Benzenesulfonamides
Medchemexpress LLC HY-15517A 5mg Medchemexpress, KN-92 (phosphate) CAS:1135280-28-2 Purity:>98%
Medchemexpress, HY-15517A 5mg KN-92 (phosphate) CAS:1135280-28-2 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.
Sigma Aldrich Fine Chemicals Biosciences SC-236 >=98% (HPLC) | 170569-86-5 | MFCD00941297 | 25MG
SC-236 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 401.79 | 170569-86-5 | MFCD00941297 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Glimepiride for system suitability European Pharmacopoeia (EP) Reference Standard | 93479-97-1 | MFCD00878417 |
Glimepiride for system suitability European Pharmacopoeia (EP) Reference Standard | Mol Wt: 490.62 | 93479-97-1 | MFCD00878417 |
Sigma Aldrich Fine Chemicals Biosciences Tamsulosin hydrochloride >=98% (HPLC) | 106463-17-6 | MFCD00922997 | 10MG
Tamsulosin hydrochloride >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 444.97 | 106463-17-6 | MFCD00922997 | 10MG
Apexbio Technology LLC Sulfasalazine 599-79-1 5g
Sulfasalazine (599-79-1) is a small-molecule inhibitor targeting the NF- B signaling pathway and the cystine-glutamate antiporter system (system Xc-) It is designed to suppress NF- B activation and inhibit cystine uptake thereby modulating inflammatory gene expression and intracellular glutathione synthesis Sulfasalazine exerts its biological activity primarily through inhibition of NF- B activation and blockade of system Xc- In in vitro studies sulfasalazine demonstrates growth inhibition and induction of apoptosis in several cancer cell lines including MIA PaCa-2 PANC-1 and glioblastoma cells with reported IC50 values ranging from approximately 0 2 to 0 5 mM depending on cell type and conditions Based on these pharmacological properties sulfasalazine holds research potential in inflammation NF- B signaling oxidative stress modulation and cancer studies
Medchemexpress LLC Deltasonamide 2 hydrochloride | 2448341-55-5 | 99.8% | 5 MG
Deltasonamide 2 hydrochloride is the hydrochloride salt of Deltasonamide 2, a competitive, high-affinity inhibitor of PDEδ (phosphodiesterase delta) with a reported Kd of ~385 pM. It is supplied as a solid research reagent, soluble in DMSO and water, and intended for biochemical and cellular studies probing PDEδ function.
- High reported binding affinity to PDEδ (Kd ~385 pM).
- High purity (reported 99.78%).
- Molecular weight 683.71 g/mol and formula C30H40Cl2N6O4S2.
- Hydrochloride salt form provided as a solid.
- Soluble in DMSO and water for assay preparation.
- Suitable for biochemical and cellular research applications.
eMolecules Ambeed / 1-(Phenylsulfonyl)-4-(4455-tetramethyl-132-dioxaborolan-2-yl)-1H-indole / 250mg / 728126188 / A1672659 / / 1334950-73-0 / MFCD12828205 / 383.270 / C20H22BNO4S
Ambeed / 1-(Phenylsulfonyl)-4-(4455-tetramethyl-132-dioxaborolan-2-yl)-1H-indole / 250mg / 728126188 / A1672659 / / 1334950-73-0 / MFCD12828205 / 383.270 / C20H22BNO4S
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
Sigma Aldrich Fine Chemicals Biosciences SC-236 >=98% (HPLC) | 170569-86-5 | MFCD00941297 | 5MG
SC-236 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 401.79 | 170569-86-5 | MFCD00941297 | 5MG
Sigma Aldrich Fine Chemicals Biosciences Tamsulosin hydrochloride British Pharmacopoeia (BP) Reference Standard | 106463-17-6 | MFCD00922997 |
Tamsulosin hydrochloride British Pharmacopoeia (BP) Reference Standard | Mol Wt: 444.97 | 106463-17-6 | MFCD00922997 |
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 Citrate (Generic Viagra) 100mg, 30 Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Sildenafil Citrate (Generic Viagra) 100mg, 30 Tablets
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 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