Benzenesulfonamides
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NXT629, MedChemExpress
MedChemExpress NXT629 is a potent, selective, and competitive PPAR-α antagonist, with an IC50 of 77 nM for human PPARα, shows high selectivity over other nuclear hormone receptor, such as PPARδ, PPARγ, ERβ, GR and TRβ, IC50s are 6.0, 15, 15.2, 32.5 and >100 μM, respectively. NXT629 has potent anti-tumor activity and inhibits experimental metastasis of cancer cell in animal models.
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| Molecular Weight (g/mol) | 609.78 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | NXT629 |
| Grade | Research |
| SMILES | O=S(C1=CC=CC=C1)(NC2=CC=C(C3=CC=C(CCCC(N4CC)=NN(CC5=CC=C(C(C)(C)C)C=C5)C4=O)C=C3)N=C2)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.2% |
| CAS | 1454925-59-7 |
| Solubility Information | DMSO : 125 mg/mL (204.99 mM; Need ultrasonic) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C35H39N5O3S |
| Formula Weight | 609.78 |
TG101209, MedChemExpress
MedChemExpress TG101209 is a selective JAK2 inhibitor with IC50 of 6 nM, less potent to Flt3 and RET with IC50 of 25 nM and 17 nM, appr 30-fold selective for JAK2 than JAK3, and sensitive to JAK2V617F and MPLW515L/K mutations.
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| Molecular Weight (g/mol) | 509.67 |
|---|---|
| Color | Gray |
| Physical Form | Solid |
| Chemical Name or Material | TG101209 |
| Grade | Research |
| SMILES | O=S(C1=CC=CC(NC2=NC(NC3=CC=C(C=C3)N4CCN(CC4)C)=NC=C2C)=C1)(NC(C)(C)C)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.81% |
| CAS | 936091-14-4 |
| Solubility Information | DMSO : ≥ 50 mg/mL (98.10 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C26H35N7O2S |
| Formula Weight | 509.67 |
Acetohexamide, MedChemExpress
MedChemExpress Acetohexamide is a first-generation sulfonylurea medication used to treat diabetes mellitus type 2; stimulate the pancreas to secrete insulin.
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| Molecular Weight (g/mol) | 324.4 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Acetohexamide |
| Grade | Research |
| SMILES | O=S(C1=CC=C(C(C)=O)C=C1)(NC(NC2CCCCC2)=O)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.39% |
| CAS | 968-81-0 |
| Solubility Information | DMSO : 25 mg/mL (77.07 mM; Need ultrasonic) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C15H20N2O4S |
| Formula Weight | 324.4 |
HMN-176, MedChemExpress
MedChemExpress HMN-176 is a stilbene derivative which inhibits mitosis, interfering with polo-like kinase-1 (plk1), without significant effect on tubulin polymerization.
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| Molecular Weight (g/mol) | 382.43 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | HMN-176 |
| Grade | Research |
| SMILES | O=S(C1=CC=C(OC)C=C1)(NC2=CC=CC=C2/C=C/C3=CC=N(C=C3)=O)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.54% |
| CAS | 173529-10-7 |
| Solubility Information | DMSO : ≥ 30 mg/mL (78.45 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C20H18N2O4S |
| Formula Weight | 382.43 |
Alofanib, MedChemExpress
MedChemExpress Alofanib (RPT835) is a potent and selective allosteric inhibitor of fibroblast growth factor receptor 2 (FGFR2). Anticancer and antiangiogenic activity.
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| Molecular Weight (g/mol) | 413.4 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Alofanib |
| Grade | Research |
| SMILES | O=C(O)C1=CC=CC(S(=O)(NC2=CC(C3=CC=CN=C3)=C(C)C=C2[N+]([O-])=O)=O)=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.81% |
| CAS | 1612888-66-0 |
| Solubility Information | DMSO : ≥ 30.1 mg/mL (72.81 mM) |
| Synonym | RPT835 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C19H15N3O6S |
| Formula Weight | 413.4 |
L755507, MedChemExpress
MedChemExpress L755507 is a potent, selective agonist of β3-AR with an IC50 of 35 nM. L755507 enhances the homology-directed repair (HDR)-mediated genome editing in CRISPR/Cas9 nickase system.
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LX2343, MedChemExpress
MedChemExpress 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.
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| Molecular Weight (g/mol) | 474.91 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | LX2343 |
| Grade | Research |
| SMILES | O=C(NC1=CC=C(OCO2)C2=C1)CN(C3=CC(Cl)=CC=C3OC)S(=O)(C4=CC=CC=C4)=O |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 99.74% |
| CAS | 333745-53-2 |
| Solubility Information | DMSO : ≥ 100 mg/mL (210.57 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C22H19ClN2O6S |
| Formula Weight | 474.91 |
SU11274, MedChemExpress
MedChemExpress SU11274 is a selective Met inhibitor with IC50 of 10 nM, but has no effects on PGDFRβ, EGFR or Tie2.
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| Molecular Weight (g/mol) | 568.09 |
|---|---|
| Color | Orange |
| Physical Form | Solid |
| Chemical Name or Material | SU11274 |
| Grade | Research |
| SMILES | O=S(C1=CC2=C(C=C1)NC(/C2=C/C3=C(C(C(N4CCN(CC4)C)=O)=C(N3)C)C)=O)(N(C)C5=CC=CC(Cl)=C5)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.19% |
| CAS | 658084-23-2 |
| Solubility Information | DMSO : ≥ 100 mg/mL (176.03 mM) |
| Synonym | PKI-SU11274 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C28H30ClN5O4S |
| Formula Weight | 568.09 |
Etebenecid, MedChemExpress
MedChemExpress Etebenecid is a uricosuric agents, lower uric acid levels in the body by increasing the elimination of uric acid by the kidneys, also inhibits penicillin tubular secretion.
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Veralipride, MedChemExpress
MedChemExpress Veralipride is a D2 receptor antagonist. It is an alternative antidopaminergic treatment for menopausal symptoms.
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| Molecular Weight (g/mol) | 383.46 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Veralipride |
| Grade | Research |
| SMILES | O=C(NCC1N(CC=C)CCC1)C2=CC(S(=O)(N)=O)=CC(OC)=C2OC |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 99.57% |
| CAS | 66644-81-3 |
| Solubility Information | DMSO : ≥ 100 mg/mL (260.78 mM) |
| Synonym | (±)-Veralipride LIR166 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C17H25N3O5S |
| Formula Weight | 383.46 |
Hydroxyhexamide, MedChemExpress
MedChemExpress Hydroxyhexamide is a pharmacologically active metabolite of Acetohexamide, used as a hypoglycemic agents.
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| Molecular Weight (g/mol) | 326.41 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Hydroxyhexamide |
| Grade | Research |
| SMILES | O=S(C1=CC=C(C(O)C)C=C1)(NC(NC2CCCCC2)=O)=O |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.68% |
| CAS | 3168-01-2 |
| Solubility Information | DMSO : ≥ 300 mg/mL (919.09 mM) |
| Synonym | (±)-Hydroxyhexamid |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C15H22N2O4S |
| Formula Weight | 326.41 |
Sulfamethoxypyridazine, MedChemExpress
MedChemExpress Sulfamethoxypyridazine is a long-acting sulfonamide antibiotic, for treatment of Dermatitis herpetiformis.
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PKR-IN-2, MedChemExpress
MedChemExpress PKR-IN-2 is a pyruvate kinase isoform PKR activator extracted from patent WO2014139144A1, compound 160. PKR-IN-2 can be used for the research of PKR function related diseases, including cancer, diabetes, obesity, autoimmune disorders, and benign prostatic hyperplasia.
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| Molecular Weight (g/mol) | 468.57 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | PKR-IN-2 |
| Grade | Research |
| SMILES | N1C2C(=C(S(NC3=CC=C(C(N4CCC(O)(CC(C)C)CC4)=O)C=C3)(=O)=O)C=CC=2)N=CC=1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 95.14% |
| CAS | 1628428-01-2 |
| Solubility Information | DMSO : 50 mg/mL (106.71 mM; Need ultrasonic) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C24H28N4O4S |
| Formula Weight | 468.57 |
PF-06471553, MedChemExpress
MedChemExpress PF-06471553 is a potent, selective and orally available monoacylglycerol acyltransferase 3 (MGAT3) inhibitor, with an IC50 of 92 nM.
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| Molecular Weight (g/mol) | 467.54 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | PF-06471553 |
| Grade | Research |
| SMILES | O=S(C1=CC2=C(CN(C(CC3=CC=CC(OC)=C3)=O)C2)C=C1)(NC4=NN(C5CCC5)N=C4)=O |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 98.18% |
| CAS | 1808094-07-6 |
| Solubility Information | DMSO : ≥ 150 mg/mL (320.83 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C23H25N5O4S |
| Formula Weight | 467.54 |
AZD2098, MedChemExpress
MedChemExpress AZD2098 is a potent and selective CC-chemokine receptor 4 (CCR4) inhibitor with pIC50s of 7.8, 8.0, 8.0 and 7.6 for human, rat, mouse and dog respectively, used for asthma research.
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| Molecular Weight (g/mol) | 334.18 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | AZD2098 |
| Grade | Research |
| SMILES | O=S(C1=CC=CC(Cl)=C1Cl)(NC2=NC=CN=C2OC)=O |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.86% |
| CAS | 566203-88-1 |
| Solubility Information | DMSO : 100 mg/mL (299.24 mM; Need ultrasonic) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C11H9Cl2N3O3S |
| Formula Weight | 334.18 |